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MyeloMATCH MSRP: En screeningsundersøgelse for at tildele mennesker med myeloid kræft til en behandlingsundersøgelse

30. oktober 2026 opdateret af: National Cancer Institute (NCI)

Master Screening and Reassessment Protocol (MSRP) for NCI MyeloMATCH kliniske forsøg

This MyeloMATCH Master Screening and Reassessment Protocol (MSRP) evaluates the use of a screening tool and specific laboratory tests to help improve participants' ability to register to clinical trials throughout the course of their myeloid cancer (acute myeloid leukemia or myelodysplastic syndrome) treatment. This study involves testing patients' bone marrow and blood for certain biomarkers. A biomarker (sometimes called a marker) is any molecule in the body that can be measured. Doctors look at markers to learn what is happening in the body. Knowing about certain markers can give doctors more information about what is driving the cancer and how to treat it. Testing patients' bone marrow and blood will show doctors if patients have markers that specific drugs can target. The marker testing in this study will let doctors know if they can match patients with a treatment study (myeloMATCH clinical trial) that tests treatment for the type of cancer they have or continue standard of care treatment with their doctor on the Tier Advancement Pathway (TAP).

Studieoversigt

Status

Rekruttering

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

PRIMARY OBJECTIVES:

I. Screening and Reassessment (MSRP): To evaluate the feasibility of MATCHBox receiving and organizing all data needed for assignment to a myeloMATCH clinical trial or Tier Advancement Pathway (TAP) within 72 hours of MDNet receipt of all required specimens for initial therapy and within 10 days for subsequent therapy.

II. Tier Advancement Pathway (TAP): To enable participants who are not matched to an investigational myeloMATCH treatment substudy to receive standard of care (SOC) while remaining on the MSRP to maintain access to later tiers of treatment substudies.

SECONDARY OBJECTIVES:

I. Screening and Reassessment (MSRP):

Ia. To describe the time to generation of all data required for treatment substudy (or TAP) assignment, time to treatment substudy (or TAP) assignment, percent assigned to a myeloMATCH treatment substudy, and the percent of screened participants who register to a myeloMATCH investigational treatment substudy or are assigned to TAP:

Iai. Separately within each tier of myeloMATCH treatment substudy and analogous TAP assignment; Ibi. Separately within each clinical basket of myeloMATCH treatment substudies; Ici. Over time, across and within the categories above.

II. Tier Advancement Pathway (TAP):

IIa. To evaluate participants for assignment to higher tier treatment substudies within myeloMATCH; IIb. To describe, within tier- and basket- levels of TAP, measurable residual disease (MRD) rates and clonal evolution; IIc. To describe, within tier- and basket- levels of TAP, remission status and overall survival of participants who receive standard of care therapy; IId. To obtain MDNet specimens for translational medicine and biobanking.

OUTLINE:

REGISTRATION: Patients undergo bone marrow aspiration and collection of blood on study. Patients' bone marrow and blood specimens undergo rapid genetic testing. Patients are then assigned to a specific substudy containing a therapy targeted to the patient's mutational profile. If there is no targetable mutation, the patient is placed on a substudy testing novel combinations that do not contain a target-specific drug. Patients who are not eligible for any MYELOMATCH substudy are assigned to TAP.

TAP: Patients continue SOC treatment and undergo continued bone marrow aspiration and blood collection for possible future substudy assignment.

TREATMENT: Patients are assigned to a specific treatment substudy.

MM1YA-CTG01: Younger patients (age 18-59 years) with intermediate risk acute myeloid leukemia (AML) are randomized to 1 of 3 arms.

ARM I: Patients receive daunorubicin intravenously (IV) on days 2-4, cytarabine IV continuously on days 2-8, and venetoclax orally (PO) once daily (QD) on days 1-11. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Based on a bone marrow aspiration assessment (completed at the discretion of the treating investigator), patients may receive reinduction consisting of daunorubicin IV on days 2-3, cytarabine IV continuously on days 2-6, and venetoclax PO QD on days 1-8. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow aspiration and collection of blood samples on study and as clinically indicated. Additionally, patients undergo echocardiography (ECHO) or multigated acquisition scan (MUGA) during screening.

ARM II: Patients receive azacitidine IV or subcutaneously (SC) on days 1-7 or days 1-5 and 8-9 and venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for a total of 2 cycles, in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow aspiration and collection of blood samples on study and as clinically indicated. Additionally, patients undergo ECHO or MUGA during screening.

ARM III: Patients receive daunorubicin IV on days 1-3 and cytarabine IV, continuously, on days 1-7. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Based on a bone marrow aspiration assessment (completed at the discretion of the treating investigator), patients may receive reinduction consisting of cytarabine IV, continuously, on days 1-5 and daunorubicin IV on days 1-2. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow aspiration and collection of blood samples on study and as clinically indicated. Additionally, patients undergo ECHO or MUGA during screening.

MM1YA-S01: Younger patients (age 18-59 years) with high-risk AML are randomized to 1 of 5 arms.

ARM I: Patients receive cytarabine IV continuously on days 1-7 and daunorubicin IV on days 1-3 per standard approach of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of cytarabine IV continuously on days 1-5 and daunorubicin IV on days 1-2. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.

ARM II: Patients receive cytarabine IV continuously on days 2-8 and daunorubicin IV on days 2-4 with venetoclax PO on days 1-11 of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of cytarabine IV continuously on days 2-6 and daunorubicin IV on days 2-3 with venetoclax PO on days 1-8. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.

ARM III: Patients receive azacitidine SC or IV on days 1-7 and venetoclax PO on days 1-28 of each cycle. Cycles repeat every 28 days for 2 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.

ARM IV: Patients receive daunorubicin and cytarabine liposome IV over 90 minutes on days 1, 3, and 5 of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of daunorubicin and cytarabine liposome IV over 90 minutes on days 1 and 3. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.

ARM V: Patients receive daunorubicin and cytarabine liposome IV over 90 minutes on days 1, 3, and 5 and venetoclax PO on days 1-14 of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of daunorubicin and cytarabine liposome IV over 90 minutes on days 1 and 3 and venetoclax PO on days 1-7. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.

MM2YA-EA01: Younger patients (age 18-59 years) with AML or secondary AML who have completed a tier 1 MyeloMATCH treatment study with complete remission (CR) or CR with partial hematologic recovery (CRh) and have detectable minimal residual disease (MRD) (> 0.1%) are randomized to 1 of 4 arms.

ARM A: Patients receive cytarabine IV on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.

ARM B: Patients receive cytarabine IV and venetoclax PO on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.

ARM C: Patients receive Vyxeos IV and venetoclax PO on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.

ARM D: Patients receive azacitidine IV or SC and venetoclax PO on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.

MM1OA-EA02: Patients are randomized to 1 of 3 regimens.

REGIMEN 1:

INDUCTION: Patients receive azacitidine IV or SC on days 1-7 of each cycle and venetoclax PO on days 1-28 of each cycle. Treatment repeats every 28 days for up to 2 cycles or until bone marrow assessment shows at least an MLFS response or better ("better" defined as CR, CRi, CRh), in the absence of disease progression or unacceptable toxicity.

CONSOLIDATION: Patients receive azacitidine IV or SC on days 1-7 and venetoclax PO on days 1-28 of each cycle. Cycles repeat every 28 days for 2 years in the absence of disease progression or unacceptable toxicity.

REGIMEN 2:

INDUCTION: Patients receive azacitidine IV or SC on days 1-7 and venetoclax and gilteritinib PO on days 1-28 of each cycle. Treatment repeats every 28 days for up to 2 cycles or until bone marrow assessment shows at least an MLFS response or better ("better" defined as CR, CRi, CRh), in the absence of disease progression or unacceptable toxicity.

CONSOLIDATION: Patients receive azacitidine IV or SC on days 1-5, venetoclax PO on days 1-7 and gilteritinib PO on days 1-28 of each cycle. Cycles repeat every 28 days for 2 years in the absence of disease progression or unacceptable toxicity.

REGIMEN 3:

INDUCTION: Patients receive azacitidine IV or SC on days 1-7 and venetoclax PO on days 1-28, and gilteritinib PO on days 8-21 of each cycle. Treatment repeats every 28 days for up to 2 cycles or until bone marrow assessment shows at least an MLFS response or better ("better" defined as CR, CRi, CRh), in the absence of disease progression or unacceptable toxicity.

CONSOLIDATION: Patients receive azacitidine IV or SC on days 1-5, venetoclax PO on days 1-14 and gilteritinib PO on days 8-21 of each cycle. Cycles repeat every 28 days for 2 years in the absence of disease progression or unacceptable toxicity.

MM1MDS-A01: Patients are randomized to 1 of 2 regimens.

REGIMEN 1: Patients receive ASTX727 PO QD on days 1-5 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients who do not achieve a CR, CRL, or CRh at the end of cycle 6 may cross-over to Regimen 1. Patients who experience CR, PR, or stable disease (SD) any time after 4 cycles of treatment may be reassessed in order to go to a higher myeloMATCH tier assignment or to TAP. Patients also undergo bone marrow biopsy and aspiration throughout the study. Patients may also undergo optional buccal swab on study, and/or optional additional bone marrow aspiration and blood sample collection on study and at disease progression.

REGIMEN 2: Patients receive ASTX727 PO QD on days 1-5 and enasidenib PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients who experience CR, PR, or SD any time after 4 cycles of treatment may be reassessed in order to go to a higher myeloMATCH tier assignment or to TAP. Patients also undergo bone marrow biopsy and aspiration throughout the study. Patients may also undergo optional buccal swab on study, and/or optional additional bone marrow aspiration and blood sample collection on study and at disease progression.

MM1OA-S03: Patients are randomized to 1 of 2 arms.

ARM 1: Patients receive ASTX727 PO QD on days 1-5 and venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo blood sample collection, bone marrow aspiration, and bone marrow biopsy throughout the trial.

ARM 2: Patients receive ASTX727 PO QD on days 1-5, venetoclax PO QD on days 1-28, and enasidenib PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo blood sample collection, bone marrow aspiration, and bone marrow biopsy throughout the trial.

MM1YA-A04: Patients are randomized to 1 of 2 regimens.

REGIMEN 1: Patients receive gemtuzumab ozogamicin IV on day 1, 2 or 3 and on day 4, 5, or 6 (NOTE: two doses must be at least 3 days apart), as well as cytarabine IV, continuously, on days 1-7 and daunorubicin IV on days 1-3 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or MUGA scan during screening, as well as bone marrow aspiration and blood sample collection throughout the study.

REGIMEN 2: Patients receive venetoclax PO QD on days 1-11, cytarabine IV, continuously, on days 2-8 and daunorubicin IV on days 2-4 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or MUGA scan during screening and bone marrow aspiration, as well as blood sample collection throughout the study.

MM3TCT-A03: Patients with matched donors are randomized to conditioning 1A or 1B. Patients with haploidentical or mismatched unrelated donors are randomized to conditioning 2A or 2B.

CONDITIONING 1A: Patients receive venetoclax PO QD on days -10 to -2, fludarabine IV on days -6 or -5 to -2 and busulfan IV on days -3 to -2 or twice daily (BID) on days -5 to -2 or melphalan IV on day -2. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity.

CONDITIONING 1B: Patients receive placebo PO QD on days -10 to -2, fludarabine IV on days -6 or -5 to -2 and busulfan IV on days -3 to -2 or BID on days -5 to -2 or melphalan IV on day -2. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity.

CONDITIONING 2A: Patients receive venetoclax PO QD on days -10 to -2, melphalan IV on day -6, fludarabine IV on days -5 to -2 and undergo total body irradiation once on day -1. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity.

CONDITIONING 2B: Patients receive placebo PO QD on days -10 to -2, melphalan IV on day -6, fludarabine IV on days -5 to -2 and undergo total body irradiation once on day -1. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity.

MAINTENANCE: All patients without evidence of relapse at day +100 are re-randomized to maintenance I or II.

MAINTENANCE I: Patients receive venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for up to 1 year post transplant (9 cycles) in the absence of disease progression or unacceptable toxicity.

MAINTENANCE II: Patients receive placebo PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for up to 1 year post transplant (9 cycles) in the absence of disease progression or unacceptable toxicity.

Patients undergo chest x-ray, echocardiography or MUGA during screening, and bone marrow biopsy and blood, urine and buccal swab collection throughout the study. Patients may also undergo positron emission tomography (PET) scan and/or computed tomography (CT) scan throughout the study.

MM1OA-MDS-A05: Patients are assigned to 1 of 3 cohorts.

COHORT A: Patients are randomized to 1 of 2 arms.

ARM 1: Patients receive ASTX727 PO QD on days 1-5 of each cycle and venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for 4 cycles in the absence of disease progression or unacceptable toxicity. Patients with CR, CRh, or CRi after cycle 4 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.

ARM 2: Patients receive ASTX727 PO QD on days 1-5 of each cycle, venetoclax PO QD on days 1-28 of each cycle, and olutasidenib PO BID on days 1-28 of each cycle. Cycles repeat every 28 days for 4 cycles in the absence of disease progression or unacceptable toxicity. Patients with CR, CRh, or CRi after cycle 4 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.

COHORT B: Patients are randomized to 1 of 2 arms.

ARM 3: Patients receive ASTX727 PO QD on days 1-5 of each cycle and olutasidenib PO BID on days 1-28 of each cycle. Cycles repeat every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients with CR continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.

ARM 4: Patients receive ASTX727 PO QD on days 1-5 of each cycle. Cycles repeat every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients without CR after cycle 6 may then cross-over to Arm 3. Patients with CR, as well as patients without CR but deriving clinical benefit after cycle 6 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.

COHORT C: Patients receive olutasidenib PO BID on days 1-28 of each cycle. Cycles repeat every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients deriving clinical benefit after cycle 6 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.

MM1MDS-CTG02: This is a dose-escalation study of luspatercept in combination, dependent upon arms assignments, with fixed dose epoetin alfa or emavusertib. Patients are randomized to 1 of 3 arms.

ARM 1: Patients receive luspatercept SC on day 1 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.

ARM 2: Patients receive luspatercept SC on day 1 and epoetin alfa SC once weekly (QW) for each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.

ARM 3: Patients receive luspatercept SC on day 1 and emavusertib PO BID on days 1-21 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.

MM1YA-EA05: Patients are randomized to 1 of 2 arms.

ARM A:

INDUCTION: Patients receive cytarabine IV, over 24 hours, on days 1-7, daunorubicin IV on days 1-3, and quizartinib PO QD on days 8-21 in the absence of disease progression or unacceptable toxicity. Patients then undergo bone marrow aspiration/biopsy. Patients with ≥ 20% bone marrow cellularity and > 5% bone marrow leukemic blasts may repeat induction as described starting on day 28-45. Patients with ≥ 20% bone marrow cellularity and ≤ 5% bone marrow leukemic blasts proceed to consolidation, following count recovery, by 30 days post-confirmation of CR/CRi. Patients with < 20% bone marrow cellularity and > 5% bone marrow leukemic blasts repeat the bone marrow aspiration/biopsy 1 week later and then either repeat induction or proceed to consolidation, based on results. Patients with < 20% bone marrow cellularity and ≤ 5% bone marrow leukemic blasts proceed to consolidation.

CONSOLIDATION: Patients receive cytarabine IV, over 1-3 hours, every 12 hours on days 1, 3 and 5 and quizartinib PO QD on days 6-19 in the absence of disease progression or unacceptable toxicity.

ARM B:

CYCLE 1: Patients receive azacitidine IV or SC on days 1-7 or days 1-5 and 8-9, venetoclax PO QD on days 1-28, and quizartinib PO QD on days 1-28 in the absence of disease progression or unacceptable toxicity and based on bone marrow findings. Patients undergo bone marrow aspiration/biopsy on day 14 of cycle 1. Patients with ≥ 20% bone marrow cellularity and > 5% bone marrow leukemic blasts continue treatment as described through day 28 of cycle 1 and then proceed to cycle 2 without interruption or delay, as long as repeat bone marrow aspiration/biopsy on day 28 of cycle 1 is consistent with persistent blasts > 5%. Patients with ≥ 20% bone marrow cellularity and ≤ 5% bone marrow leukemic blasts interrupt venetoclax and quizartinib for the remainder of the cycle (through day 28) and then proceed to cycle 2 of treatment as described following count recovery. Patients without count recovery by day 42 undergo repeat bone marrow aspiration/biopsy. Patients with count recovery by day 42 proceed to cycle 2 (by day 50). For patients without count recovery by day 50 whose repeat bone marrow aspiration/biopsy shows no blasts, initiation of cycle 2 will be discussed with the study chairs. Patients with < 20% bone marrow cellularity and > 5% bone marrow leukemic blasts interrupt venetoclax and quizartinib, undergo repeat bone marrow aspiration/biopsy 1 week later, and proceed based on repeat biopsy results as described. Patients with < 20% bone marrow cellularity and ≤ 5% bone marrow leukemic blasts interrupt venetoclax and quizartinib for the remainder of the cycle (through day 28) and then proceed to cycle 2 of treatment as described following count recovery. Patients without count recovery by day 42 undergo repeat bone marrow aspiration/biopsy. Patients with count recovery by day 42 proceed to cycle 2 (by day 50). For patients without count recovery by day 50 whose repeat bone marrow aspiration/biopsy shows no blasts, initiation of cycle 2 will be discussed with the study chairs.

CYCLE 2: Patients receive azacitidine IV or SC on days 1-7 or days 1-5 and 8-9, venetoclax PO QD on days 1-28, and quizartinib PO QD on days 1-28 in the absence of disease progression or unacceptable toxicity and based on bone marrow findings. Patients who do not achieve response after completion of cycle 1 undergo bone marrow aspiration/biopsy on day 14 of cycle 2. Patients with ≥ 20% bone marrow cellularity and > 5% bone marrow leukemic blasts continue venetoclax and quizartinib as described through day 28 of cycle 2. Patients with ≥ 20% bone marrow cellularity and ≤ 5% bone marrow leukemic blasts interrupt venetoclax and quizartinib for the remainder of the cycle (through day 28). Patients with < 20% bone marrow cellularity and > 5% bone marrow leukemic blasts interrupt venetoclax and quizartinib, undergo repeat bone marrow aspiration/biopsy 1 week later, and proceed based on repeat aspiration/biopsy results as described. Patients with < 20% bone marrow cellularity and ≤ 5% bone marrow leukemic blasts interrupt venetoclax and quizartinib for the remainder of the cycle (through day 28).

Upon completion of two cycles of therapy on either Arm A or Arm B, patients who are eligible can proceed to allogeneic stem cell transplant; while awaiting allogeneic stem cell transplant, patients should continue standard of care therapy.

Patients undergo echocardiography or MUGA scan during screening and undergo bone marrow aspiration and biopsy as well as blood sample collection throughout the study.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

2000

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Canada
    • Alberta
      • Calgary, Alberta, Canada, T2N 5G2
        • Rekruttering
        • Arthur J E Child Comprehensive Cancer Centre
        • Kontakt:
        • Ledende efterforsker:
          • Mary L. Savoie
      • Edmonton, Alberta, Canada, T6G 2B7
        • Rekruttering
        • University of Alberta Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Joseph M. Brandwein
    • Manitoba
      • Winnipeg, Manitoba, Canada, R3E 0V9
        • Rekruttering
        • CancerCare Manitoba
        • Kontakt:
        • Ledende efterforsker:
          • Brett L. Houston
    • Nova Scotia
      • Halifax, Nova Scotia, Canada, B3H 2Y9
        • Rekruttering
        • QEII Health Sciences Centre/Nova Scotia Health Authority
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 902-473-6000
        • Ledende efterforsker:
          • Mahmoud Elsawy
    • Ontario
      • Hamilton, Ontario, Canada, L8V 5C2
        • Rekruttering
        • Juravinski Cancer Centre at Hamilton Health Sciences
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 905-387-9495
        • Ledende efterforsker:
          • Alejandro Garcia-Horton
      • Ottawa, Ontario, Canada, K1H 8L6
        • Rekruttering
        • Ottawa Hospital and Cancer Center-General Campus
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 613-761-4395
        • Ledende efterforsker:
          • Mitchell Sabloff
      • Toronto, Ontario, Canada, M5G 2M9
        • Suspenderet
        • University Health Network-Princess Margaret Hospital
      • Toronto, Ontario, Canada, M4N 3M5
        • Rekruttering
        • Odette Cancer Centre- Sunnybrook Health Sciences Centre
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 416-480-5000
        • Ledende efterforsker:
          • Rena J. Buckstein
    • Quebec
      • Greenfield Park, Quebec, Canada, J4V 2H1
        • Rekruttering
        • CSSS Champlain-Charles Le Moyne
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 450-466-5065
        • Ledende efterforsker:
          • Sami Morin-Ben Abdallah
      • Montreal, Quebec, Canada, H3T 1E2
        • Rekruttering
        • Jewish General Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 8248 514-340-8222
        • Ledende efterforsker:
          • Sarit E. Assouline
      • Montreal, Quebec, Canada, H1T 2M4
        • Rekruttering
        • CIUSSSEMTL-Hopital Maisonneuve-Rosemont
        • Ledende efterforsker:
          • Julie Bergeron
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 3329 514-252-3400
  • Forenede Stater
    • Alabama
      • Birmingham, Alabama, Forenede Stater, 35233
        • Rekruttering
        • University of Alabama at Birmingham Cancer Center
        • Ledende efterforsker:
          • Razan Mohty
        • Kontakt:
    • Arizona
      • Phoenix, Arizona, Forenede Stater, 85054
        • Rekruttering
        • Mayo Clinic Hospital in Arizona
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 855-776-0015
        • Ledende efterforsker:
          • James M. Foran
      • Tucson, Arizona, Forenede Stater, 85719
        • Rekruttering
        • Banner University Medical Center - Tucson
        • Ledende efterforsker:
          • Sharad Khurana
        • Kontakt:
      • Tucson, Arizona, Forenede Stater, 85719
        • Rekruttering
        • University of Arizona Cancer Center-North Campus
        • Ledende efterforsker:
          • Sharad Khurana
        • Kontakt:
    • Arkansas
      • Little Rock, Arkansas, Forenede Stater, 72205
        • Rekruttering
        • University of Arkansas for Medical Sciences
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 501-686-8274
        • Ledende efterforsker:
          • Ankur Varma
    • California
      • Berkeley, California, Forenede Stater, 94704
        • Aktiv, ikke rekrutterende
        • Alta Bates Summit Medical Center-Herrick Campus
      • Dublin, California, Forenede Stater, 94568
        • Rekruttering
        • Kaiser Permanente Dublin
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Fremont, California, Forenede Stater, 94538
        • Rekruttering
        • Kaiser Permanente-Fremont
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Fresno, California, Forenede Stater, 93720
        • Suspenderet
        • Kaiser Permanente-Fresno
      • Fresno, California, Forenede Stater, 93720
        • Rekruttering
        • Kaiser Permanente Fresno Orchard Plaza
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 833-574-2273
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Irvine, California, Forenede Stater, 92612
        • Rekruttering
        • UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care
        • Ledende efterforsker:
          • Deepa Jeyakumar
        • Kontakt:
      • Long Beach, California, Forenede Stater, 90822
        • Aktiv, ikke rekrutterende
        • Tibor Rubin VA Medical Center
      • Los Angeles, California, Forenede Stater, 90048
        • Rekruttering
        • Cedars-Sinai Medical Center
        • Ledende efterforsker:
          • Noah M. Merin
        • Kontakt:
      • Modesto, California, Forenede Stater, 95356
        • Suspenderet
        • Kaiser Permanente-Modesto
      • Modesto, California, Forenede Stater, 95356
        • Rekruttering
        • Kaiser Permanente- Modesto MOB II
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Oakland, California, Forenede Stater, 94611
        • Rekruttering
        • Kaiser Permanente-Oakland
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Orange, California, Forenede Stater, 92868
        • Rekruttering
        • UC Irvine Health/Chao Family Comprehensive Cancer Center
        • Ledende efterforsker:
          • Deepa Jeyakumar
        • Kontakt:
      • Roseville, California, Forenede Stater, 95661
        • Rekruttering
        • Kaiser Permanente-Roseville
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Sacramento, California, Forenede Stater, 95817
        • Rekruttering
        • University of California Davis Comprehensive Cancer Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 916-734-3089
        • Ledende efterforsker:
          • Brian A. Jonas
      • Sacramento, California, Forenede Stater, 95814
        • Rekruttering
        • Kaiser Permanente Downtown Commons
        • Ledende efterforsker:
          • Faisal N. Cheema
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: kpoct@kp.org
      • Sacramento, California, Forenede Stater, 95823
        • Rekruttering
        • Kaiser Permanente-South Sacramento
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • San Francisco, California, Forenede Stater, 94115
        • Rekruttering
        • Kaiser Permanente-San Francisco
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • San Francisco, California, Forenede Stater, 94143
        • Rekruttering
        • UCSF Medical Center-Parnassus
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-827-3222
        • Ledende efterforsker:
          • Timothy Ferng
      • San Jose, California, Forenede Stater, 95119
        • Rekruttering
        • Kaiser Permanente-Santa Teresa-San Jose
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • San Leandro, California, Forenede Stater, 94577
        • Rekruttering
        • Kaiser Permanente San Leandro
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • San Rafael, California, Forenede Stater, 94903
        • Rekruttering
        • Kaiser San Rafael-Gallinas
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Santa Clara, California, Forenede Stater, 95051
        • Rekruttering
        • Kaiser Permanente Medical Center - Santa Clara
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Santa Rosa, California, Forenede Stater, 95403
        • Rekruttering
        • Kaiser Permanente-Santa Rosa
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • South San Francisco, California, Forenede Stater, 94080
        • Rekruttering
        • Kaiser Permanente-South San Francisco
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Vallejo, California, Forenede Stater, 94589
        • Rekruttering
        • Kaiser Permanente-Vallejo
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
      • Walnut Creek, California, Forenede Stater, 94596
        • Rekruttering
        • Kaiser Permanente-Walnut Creek
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Ledende efterforsker:
          • Faisal N. Cheema
    • Connecticut
      • New Haven, Connecticut, Forenede Stater, 06520
        • Rekruttering
        • Yale University
        • Kontakt:
        • Ledende efterforsker:
          • Jan P. Bewersdorf
      • West Haven, Connecticut, Forenede Stater, 06516
        • Rekruttering
        • Veterans Affairs Connecticut Healthcare System-West Haven Campus
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 2832 203-937-3421
        • Ledende efterforsker:
          • Alexander Pine
    • Florida
      • Gainesville, Florida, Forenede Stater, 32610
        • Rekruttering
        • UF Health Cancer Institute - Gainesville
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 352-273-8010
        • Ledende efterforsker:
          • Dina G. Khalaf
      • Jacksonville, Florida, Forenede Stater, 32224-9980
        • Rekruttering
        • Mayo Clinic in Florida
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 855-776-0015
        • Ledende efterforsker:
          • James M. Foran
      • Miami, Florida, Forenede Stater, 33176
        • Rekruttering
        • Miami Cancer Institute
        • Ledende efterforsker:
          • Firas El Chaer
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 786-596-2000
      • Pembroke Pines, Florida, Forenede Stater, 33028
        • Rekruttering
        • Memorial Hospital West
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 954-265-4325
        • Ledende efterforsker:
          • Yehuda E. Deutsch
      • Ruskin, Florida, Forenede Stater, 33570
        • Rekruttering
        • Moffitt Cancer Center at SouthShore
        • Ledende efterforsker:
          • Rory M. Shallis
        • Kontakt:
      • Tampa, Florida, Forenede Stater, 33607
        • Rekruttering
        • Moffitt Cancer Center-International Plaza
        • Ledende efterforsker:
          • Rory M. Shallis
        • Kontakt:
      • Tampa, Florida, Forenede Stater, 33612
        • Rekruttering
        • Moffitt Cancer Center - McKinley Campus
        • Ledende efterforsker:
          • Rory M. Shallis
        • Kontakt:
      • Tampa, Florida, Forenede Stater, 33612
        • Rekruttering
        • Moffitt Cancer Center
        • Ledende efterforsker:
          • Rory M. Shallis
        • Kontakt:
      • Wesley Chapel, Florida, Forenede Stater, 33544
        • Rekruttering
        • Moffitt Cancer Center at Wesley Chapel
        • Ledende efterforsker:
          • Rory M. Shallis
        • Kontakt:
    • Georgia
      • Albany, Georgia, Forenede Stater, 31701
        • Rekruttering
        • Phoebe Putney Memorial Hospital
        • Ledende efterforsker:
          • Vamsi Kota
        • Kontakt:
      • Augusta, Georgia, Forenede Stater, 30912
        • Rekruttering
        • Augusta University Medical Center
        • Ledende efterforsker:
          • Vamsi Kota
        • Kontakt:
    • Hawaii
      • Honolulu, Hawaii, Forenede Stater, 96826
        • Rekruttering
        • Kapiolani Medical Center for Women and Children
        • Ledende efterforsker:
          • Craig S. Boddy
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 808-983-6090
      • Honolulu, Hawaii, Forenede Stater, 96813
        • Rekruttering
        • Hawaii Cancer Care Inc - Waterfront Plaza
        • Ledende efterforsker:
          • Craig S. Boddy
        • Kontakt:
      • Honolulu, Hawaii, Forenede Stater, 96813
        • Rekruttering
        • Straub Clinic and Hospital
        • Ledende efterforsker:
          • Craig S. Boddy
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 808-522-4333
      • Honolulu, Hawaii, Forenede Stater, 96819
        • Rekruttering
        • Kaiser Permanente Moanalua Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Faisal N. Cheema
      • ‘Aiea, Hawaii, Forenede Stater, 96701
        • Rekruttering
        • Hawaii Cancer Care - Westridge
        • Ledende efterforsker:
          • Craig S. Boddy
        • Kontakt:
      • ‘Aiea, Hawaii, Forenede Stater, 96701
        • Rekruttering
        • Pali Momi Medical Center
        • Ledende efterforsker:
          • Craig S. Boddy
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 808-486-6000
    • Idaho
      • Boise, Idaho, Forenede Stater, 83712
        • Rekruttering
        • Saint Luke's Cancer Institute - Boise
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Boise, Idaho, Forenede Stater, 83706
        • Rekruttering
        • Saint Alphonsus Cancer Care Center-Boise
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Caldwell, Idaho, Forenede Stater, 83605
        • Rekruttering
        • Saint Alphonsus Cancer Care Center-Caldwell
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Coeur d'Alene, Idaho, Forenede Stater, 83814
        • Rekruttering
        • Kootenai Health - Coeur d'Alene
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
      • Fruitland, Idaho, Forenede Stater, 83619
        • Rekruttering
        • Saint Luke's Cancer Institute - Fruitland
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Meridian, Idaho, Forenede Stater, 83642
        • Rekruttering
        • Saint Luke's Cancer Institute - Meridian
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Nampa, Idaho, Forenede Stater, 83687
        • Rekruttering
        • Saint Luke's Cancer Institute - Nampa
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Nampa, Idaho, Forenede Stater, 83687
        • Rekruttering
        • Saint Alphonsus Cancer Care Center-Nampa
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Post Falls, Idaho, Forenede Stater, 83854
        • Rekruttering
        • Kootenai Clinic Cancer Services - Post Falls
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
      • Sandpoint, Idaho, Forenede Stater, 83864
        • Rekruttering
        • Kootenai Clinic Cancer Services - Sandpoint
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
    • Illinois
      • Aurora, Illinois, Forenede Stater, 60506
        • Rekruttering
        • Advocate Outpatient Center - Aurora
        • Ledende efterforsker:
          • Thomas J. Saphner
        • Kontakt:
      • Barrington, Illinois, Forenede Stater, 60010
        • Rekruttering
        • Advocate Good Shepherd Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 847-842-4847
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Bloomington, Illinois, Forenede Stater, 61704
        • Rekruttering
        • Illinois CancerCare-Bloomington
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Bloomington, Illinois, Forenede Stater, 61701
        • Rekruttering
        • OSF Saint Joseph Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Canton, Illinois, Forenede Stater, 61520
        • Rekruttering
        • Illinois CancerCare-Canton
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Carthage, Illinois, Forenede Stater, 62321
        • Rekruttering
        • Illinois CancerCare-Carthage
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Chicago, Illinois, Forenede Stater, 60637
        • Rekruttering
        • University of Chicago Comprehensive Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Olatoyosi M. Odenike
      • Chicago, Illinois, Forenede Stater, 60611
        • Rekruttering
        • Northwestern University
        • Ledende efterforsker:
          • Jessica K. Altman
        • Kontakt:
      • Chicago, Illinois, Forenede Stater, 60612
        • Rekruttering
        • University of Illinois
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 312-355-3046
        • Ledende efterforsker:
          • Noah Birch
      • Chicago, Illinois, Forenede Stater, 60657
        • Rekruttering
        • Advocate Illinois Masonic Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 773-296-5360
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Chicago, Illinois, Forenede Stater, 60612
        • Rekruttering
        • Rush MD Anderson Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Melissa L. Larson
      • Crystal Lake, Illinois, Forenede Stater, 60014
        • Rekruttering
        • AMG Crystal Lake - Oncology
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Danville, Illinois, Forenede Stater, 61832
        • Rekruttering
        • Carle at The Riverfront
        • Ledende efterforsker:
          • Suparna Mantha
        • Kontakt:
      • DeKalb, Illinois, Forenede Stater, 60115
        • Rekruttering
        • Northwestern Medicine Cancer Center Kishwaukee
        • Ledende efterforsker:
          • Jessica K. Altman
        • Kontakt:
      • Decatur, Illinois, Forenede Stater, 62526
        • Rekruttering
        • Cancer Care Specialists of Illinois - Decatur
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
      • Decatur, Illinois, Forenede Stater, 62526
        • Rekruttering
        • Decatur Memorial Hospital
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
      • Dixon, Illinois, Forenede Stater, 61021
        • Rekruttering
        • Illinois CancerCare-Dixon
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 815-285-7800
      • Downers Grove, Illinois, Forenede Stater, 60515
        • Rekruttering
        • Advocate Good Samaritan Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Effingham, Illinois, Forenede Stater, 62401
        • Rekruttering
        • Carle Physician Group-Effingham
        • Ledende efterforsker:
          • Suparna Mantha
        • Kontakt:
      • Effingham, Illinois, Forenede Stater, 62401
        • Rekruttering
        • Crossroads Cancer Center
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
      • Elgin, Illinois, Forenede Stater, 60123
        • Rekruttering
        • Advocate Sherman Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 847-429-2907
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Eureka, Illinois, Forenede Stater, 61530
        • Rekruttering
        • Illinois CancerCare-Eureka
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Evanston, Illinois, Forenede Stater, 60201
        • Rekruttering
        • NorthShore University HealthSystem-Evanston Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 847-570-2109
        • Ledende efterforsker:
          • Robert M. Eisner
      • Galesburg, Illinois, Forenede Stater, 61401
        • Rekruttering
        • Illinois CancerCare-Galesburg
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Geneva, Illinois, Forenede Stater, 60134
        • Rekruttering
        • Northwestern Medicine Cancer Center Delnor
        • Ledende efterforsker:
          • Jessica K. Altman
        • Kontakt:
      • Glenview, Illinois, Forenede Stater, 60026
        • Rekruttering
        • NorthShore University HealthSystem-Glenbrook Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 847-570-2109
        • Ledende efterforsker:
          • Robert M. Eisner
      • Glenview, Illinois, Forenede Stater, 60026
        • Rekruttering
        • Northwestern Medicine Glenview Outpatient Center
        • Ledende efterforsker:
          • Jessica K. Altman
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 312-695-1102
      • Grayslake, Illinois, Forenede Stater, 60030
        • Rekruttering
        • Northwestern Medicine Grayslake Outpatient Center
        • Ledende efterforsker:
          • Jessica K. Altman
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 312-695-1102
      • Harvey, Illinois, Forenede Stater, 60426
        • Rekruttering
        • Ingalls Memorial Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Kimberly R. Kruczek
      • Hazel Crest, Illinois, Forenede Stater, 60429
        • Rekruttering
        • Advocate South Suburban Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 708-799-9995
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Highland Park, Illinois, Forenede Stater, 60035
        • Rekruttering
        • NorthShore University HealthSystem-Highland Park Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 847-570-2109
        • Ledende efterforsker:
          • Robert M. Eisner
      • Hines, Illinois, Forenede Stater, 60141
        • Rekruttering
        • Edward Hines Jr VA Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 708-202-8387
        • Ledende efterforsker:
          • Jorgena Kosti-Schwartz
      • Kewanee, Illinois, Forenede Stater, 61443
        • Rekruttering
        • Illinois CancerCare-Kewanee Clinic
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Lake Forest, Illinois, Forenede Stater, 60045
        • Rekruttering
        • Northwestern Medicine Lake Forest Hospital
        • Ledende efterforsker:
          • Jessica K. Altman
        • Kontakt:
      • Libertyville, Illinois, Forenede Stater, 60048
        • Rekruttering
        • AMG Libertyville - Oncology
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Libertyville, Illinois, Forenede Stater, 60048
        • Rekruttering
        • Condell Memorial Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Macomb, Illinois, Forenede Stater, 61455
        • Rekruttering
        • Illinois CancerCare-Macomb
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Mattoon, Illinois, Forenede Stater, 61938
        • Rekruttering
        • Carle Physician Group-Mattoon/Charleston
        • Ledende efterforsker:
          • Suparna Mantha
        • Kontakt:
      • Maywood, Illinois, Forenede Stater, 60153
        • Rekruttering
        • Loyola University Medical Center
        • Ledende efterforsker:
          • Stephanie B. Tsai
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 708-226-4357
      • O'Fallon, Illinois, Forenede Stater, 62269
        • Rekruttering
        • Cancer Care Center of O'Fallon
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
      • Oak Lawn, Illinois, Forenede Stater, 60453-2699
        • Rekruttering
        • Advocate Christ Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 800-323-8622
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Oak Lawn, Illinois, Forenede Stater, 60453
        • Rekruttering
        • Advocate Outpatient Center - Oak Lawn
        • Ledende efterforsker:
          • Thomas J. Saphner
        • Kontakt:
      • Orland Park, Illinois, Forenede Stater, 60462
      • Ottawa, Illinois, Forenede Stater, 61350
        • Rekruttering
        • Illinois CancerCare-Ottawa Clinic
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Palos Heights, Illinois, Forenede Stater, 60463
        • Rekruttering
        • Advocate High Tech Medical Park
        • Ledende efterforsker:
          • Thomas J. Saphner
        • Kontakt:
      • Park Ridge, Illinois, Forenede Stater, 60068
        • Rekruttering
        • Advocate Lutheran General Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 847-384-3621
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Pekin, Illinois, Forenede Stater, 61554
        • Rekruttering
        • Illinois CancerCare-Pekin
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Peoria, Illinois, Forenede Stater, 61615
        • Rekruttering
        • Illinois CancerCare-Peoria
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Peoria, Illinois, Forenede Stater, 61636
        • Rekruttering
        • Methodist Medical Center of Illinois
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Peoria, Illinois, Forenede Stater, 61637
        • Rekruttering
        • OSF Saint Francis Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Peru, Illinois, Forenede Stater, 61354
        • Rekruttering
        • Illinois CancerCare-Peru
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Princeton, Illinois, Forenede Stater, 61356
        • Rekruttering
        • Illinois CancerCare-Princeton
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
      • Springfield, Illinois, Forenede Stater, 62702
        • Rekruttering
        • Southern Illinois University School of Medicine
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 217-545-7929
      • Springfield, Illinois, Forenede Stater, 62702
        • Rekruttering
        • Springfield Clinic
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 800-444-7541
      • Springfield, Illinois, Forenede Stater, 62781
        • Rekruttering
        • Springfield Memorial Hospital
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
      • Urbana, Illinois, Forenede Stater, 61801
        • Rekruttering
        • Carle Cancer Center
        • Ledende efterforsker:
          • Suparna Mantha
        • Kontakt:
      • Warrenville, Illinois, Forenede Stater, 60555
        • Rekruttering
        • Northwestern Medicine Cancer Center Warrenville
        • Ledende efterforsker:
          • Jessica K. Altman
        • Kontakt:
      • Washington, Illinois, Forenede Stater, 61571
        • Rekruttering
        • Illinois CancerCare - Washington
        • Kontakt:
        • Ledende efterforsker:
          • Bryan A. Faller
    • Indiana
      • Indianapolis, Indiana, Forenede Stater, 46202
        • Rekruttering
        • Indiana University/Melvin and Bren Simon Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Rita Assi
    • Iowa
      • Ankeny, Iowa, Forenede Stater, 50023
        • Rekruttering
        • UI Health Care Mission Cancer and Blood - Ankeny Clinic
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-241-3305
        • Ledende efterforsker:
          • Seema Harichand-Herdt
      • Clive, Iowa, Forenede Stater, 50325
        • Rekruttering
        • UI Health Care Mission Cancer and Blood - West Des Moines Clinic
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-241-3305
        • Ledende efterforsker:
          • Seema Harichand-Herdt
      • Des Moines, Iowa, Forenede Stater, 50314
        • Rekruttering
        • Mercy Medical Center - Des Moines
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-241-3305
        • Ledende efterforsker:
          • Richard L. Deming
      • Des Moines, Iowa, Forenede Stater, 50309
        • Rekruttering
        • Iowa Methodist Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-241-6727
        • Ledende efterforsker:
          • Seema Harichand-Herdt
      • Des Moines, Iowa, Forenede Stater, 50309
        • Rekruttering
        • UI Health Care Mission Cancer and Blood - Des Moines Clinic
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-241-3305
        • Ledende efterforsker:
          • Seema Harichand-Herdt
      • Des Moines, Iowa, Forenede Stater, 50314
        • Rekruttering
        • UI Health Care Mission Cancer and Blood - Laurel Clinic
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-241-3305
        • Ledende efterforsker:
          • Seema Harichand-Herdt
      • Iowa City, Iowa, Forenede Stater, 52242
        • Rekruttering
        • University of Iowa/Holden Comprehensive Cancer Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 800-237-1225
        • Ledende efterforsker:
          • Prajwal Dhakal
      • Pella, Iowa, Forenede Stater, 50219
        • Rekruttering
        • UI Healthcare Mission Cancer and Blood - Pella
        • Ledende efterforsker:
          • Seema Harichand-Herdt
        • Kontakt:
      • Waukee, Iowa, Forenede Stater, 50263
        • Rekruttering
        • UI Health Care Mission Cancer and Blood - Waukee Clinic
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-241-3305
        • Ledende efterforsker:
          • Seema Harichand-Herdt
      • West Des Moines, Iowa, Forenede Stater, 50266
        • Rekruttering
        • The Iowa Clinic PC
        • Ledende efterforsker:
          • Seema Harichand-Herdt
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 515-875-9815
    • Kansas
      • Fairway, Kansas, Forenede Stater, 66205
        • Rekruttering
        • University of Kansas Clinical Research Center
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Hays, Kansas, Forenede Stater, 67601
        • Rekruttering
        • HaysMed
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 785-623-5774
        • Ledende efterforsker:
          • Tara L. Lin
      • Kansas City, Kansas, Forenede Stater, 66160
        • Rekruttering
        • University of Kansas Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Lawrence, Kansas, Forenede Stater, 66044
        • Rekruttering
        • Lawrence Memorial Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Olathe, Kansas, Forenede Stater, 66061
        • Rekruttering
        • The University of Kansas Cancer Center - Olathe
        • Ledende efterforsker:
          • Tara L. Lin
        • Kontakt:
      • Overland Park, Kansas, Forenede Stater, 66211
        • Rekruttering
        • University of Kansas Hospital-Indian Creek Campus
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Overland Park, Kansas, Forenede Stater, 66210
        • Rekruttering
        • University of Kansas Cancer Center-Overland Park
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Salina, Kansas, Forenede Stater, 67401
        • Rekruttering
        • Salina Regional Health Center
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Topeka, Kansas, Forenede Stater, 66606
        • Rekruttering
        • University of Kansas Health System Saint Francis Campus
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 785-295-8000
        • Ledende efterforsker:
          • Tara L. Lin
      • Topeka, Kansas, Forenede Stater, 66606
        • Suspenderet
        • Cotton O'Neil Cancer Center / Stormont Vail Health
      • Westwood, Kansas, Forenede Stater, 66205
        • Rekruttering
        • University of Kansas Hospital-Westwood Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
    • Kentucky
      • Lexington, Kentucky, Forenede Stater, 40536
        • Rekruttering
        • University of Kentucky/Markey Cancer Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 859-257-3379
        • Ledende efterforsker:
          • Ayman Qasrawi
      • Louisville, Kentucky, Forenede Stater, 40202
        • Rekruttering
        • The James Graham Brown Cancer Center at University of Louisville
        • Ledende efterforsker:
          • Mohamed M. Hegazi
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 502-562-3429
      • Louisville, Kentucky, Forenede Stater, 40245
        • Rekruttering
        • UofL Health Medical Center Northeast
        • Ledende efterforsker:
          • Mohamed M. Hegazi
        • Kontakt:
    • Louisiana
      • Baton Rouge, Louisiana, Forenede Stater, 70805
        • Rekruttering
        • LSU Health Baton Rouge-North Clinic
        • Kontakt:
        • Ledende efterforsker:
          • Harry G. Sequeira Gross
      • Baton Rouge, Louisiana, Forenede Stater, 70808
        • Rekruttering
        • Our Lady of The Lake
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 225-765-7659
        • Ledende efterforsker:
          • Harry G. Sequeira Gross
      • Baton Rouge, Louisiana, Forenede Stater, 70808
        • Rekruttering
        • Our Lady of the Lake Physician Group
        • Kontakt:
        • Ledende efterforsker:
          • Harry G. Sequeira Gross
    • Maine
      • Brunswick, Maine, Forenede Stater, 04011
        • Rekruttering
        • Mid Coast Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Pamela Egan
      • Brunswick, Maine, Forenede Stater, 04011
        • Rekruttering
        • MaineHealth Cancer Care and IV Therapy - Brunswick
        • Ledende efterforsker:
          • Pamela Egan
        • Kontakt:
      • Portland, Maine, Forenede Stater, 04102
        • Rekruttering
        • MaineHealth Maine Medical Center - Portland
        • Ledende efterforsker:
          • Pamela Egan
        • Kontakt:
      • Scarborough, Maine, Forenede Stater, 04074
        • Rekruttering
        • MaineHealth Maine Medical Center- Scarborough
        • Ledende efterforsker:
          • Pamela Egan
        • Kontakt:
      • South Portland, Maine, Forenede Stater, 04106
        • Rekruttering
        • MaineHealth Cancer Care and IV Therapy - South Portland
        • Ledende efterforsker:
          • Pamela Egan
        • Kontakt:
    • Maryland
      • Baltimore, Maryland, Forenede Stater, 21287
        • Rekruttering
        • Johns Hopkins University/Sidney Kimmel Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Alexander J. Ambinder
      • Bethesda, Maryland, Forenede Stater, 20889-5600
        • Suspenderet
        • Walter Reed National Military Medical Center
    • Massachusetts
      • Boston, Massachusetts, Forenede Stater, 02215
        • Rekruttering
        • Dana-Farber Cancer Institute
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 877-442-3324
        • Ledende efterforsker:
          • Richard M. Stone
      • Boston, Massachusetts, Forenede Stater, 02215
        • Rekruttering
        • Beth Israel Deaconess Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 617-667-9925
        • Ledende efterforsker:
          • Malgorzata McMasters
      • Boston, Massachusetts, Forenede Stater, 02111
      • Worcester, Massachusetts, Forenede Stater, 01655
        • Rekruttering
        • UMass Memorial Medical Center - University Campus
        • Ledende efterforsker:
          • Jan Cerny
        • Kontakt:
    • Michigan
      • Ann Arbor, Michigan, Forenede Stater, 48106
        • Rekruttering
        • Trinity Health Saint Joseph Mercy Hospital Ann Arbor
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Brighton, Michigan, Forenede Stater, 48114
        • Rekruttering
        • Trinity Health IHA Medical Group Hematology Oncology - Brighton
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Canton, Michigan, Forenede Stater, 48188
        • Rekruttering
        • Trinity Health IHA Medical Group Hematology Oncology - Canton
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Chelsea, Michigan, Forenede Stater, 48118
        • Rekruttering
        • Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Clinton Township, Michigan, Forenede Stater, 48038
        • Rekruttering
        • Henry Ford Macomb Hospital-Clinton Township
        • Kontakt:
        • Ledende efterforsker:
          • Ahmad H. Mattour
      • Detroit, Michigan, Forenede Stater, 48201
        • Rekruttering
        • Wayne State University/Karmanos Cancer Institute
        • Ledende efterforsker:
          • Vijendra Singh
        • Kontakt:
      • Detroit, Michigan, Forenede Stater, 48202
        • Rekruttering
        • Henry Ford Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Ahmad H. Mattour
      • Farmington Hills, Michigan, Forenede Stater, 48334
        • Rekruttering
        • Weisberg Cancer Treatment Center
        • Kontakt:
        • Ledende efterforsker:
          • Vijendra Singh
      • Flint, Michigan, Forenede Stater, 48503
        • Rekruttering
        • Genesys Hurley Cancer Institute
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Flint, Michigan, Forenede Stater, 48503
        • Rekruttering
        • Hurley Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Flint, Michigan, Forenede Stater, 48503
        • Suspenderet
        • Genesee Hematology Oncology PC
      • Flint, Michigan, Forenede Stater, 48503
        • Rekruttering
        • Cancer Hematology Centers - Flint
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Jackson, Michigan, Forenede Stater, 49201
        • Rekruttering
        • Allegiance Health
        • Kontakt:
        • Ledende efterforsker:
          • Ahmad H. Mattour
      • Livonia, Michigan, Forenede Stater, 48154
        • Rekruttering
        • Trinity Health Saint Mary Mercy Livonia Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Novi, Michigan, Forenede Stater, 48377
        • Rekruttering
        • Henry Ford Medical Center-Columbus
        • Kontakt:
        • Ledende efterforsker:
          • Ahmad H. Mattour
      • Pontiac, Michigan, Forenede Stater, 48341
        • Rekruttering
        • Trinity Health Saint Joseph Mercy Oakland Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • West Bloomfield, Michigan, Forenede Stater, 48322
        • Rekruttering
        • Henry Ford West Bloomfield Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Ahmad H. Mattour
      • Ypsilanti, Michigan, Forenede Stater, 48197
        • Rekruttering
        • Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
    • Minnesota
      • Bemidji, Minnesota, Forenede Stater, 56601
      • Coon Rapids, Minnesota, Forenede Stater, 55433
        • Rekruttering
        • Mercy Hospital
        • Kontakt:
        • Ledende efterforsker:
          • David M. King
      • Deer River, Minnesota, Forenede Stater, 56636
        • Rekruttering
        • Essentia Health - Deer River Clinic
        • Kontakt:
        • Ledende efterforsker:
          • Bret E. Friday
      • Duluth, Minnesota, Forenede Stater, 55805
        • Rekruttering
        • Essentia Health Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Bret E. Friday
      • Edina, Minnesota, Forenede Stater, 55435
        • Rekruttering
        • Fairview Southdale Hospital
        • Kontakt:
        • Ledende efterforsker:
          • David M. King
      • Edina, Minnesota, Forenede Stater, 55435
        • Rekruttering
        • Minnesota Oncology - Edina
        • Kontakt:
        • Ledende efterforsker:
          • David M. King
      • Hibbing, Minnesota, Forenede Stater, 55746
        • Rekruttering
        • Essentia Health Hibbing Clinic
        • Ledende efterforsker:
          • Bret E. Friday
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 218-786-3308
      • Minneapolis, Minnesota, Forenede Stater, 55407
        • Rekruttering
        • Abbott-Northwestern Hospital
        • Kontakt:
        • Ledende efterforsker:
          • David M. King
      • Rochester, Minnesota, Forenede Stater, 55905
        • Rekruttering
        • Mayo Clinic in Rochester
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 855-776-0015
        • Ledende efterforsker:
          • James M. Foran
      • Saint Louis Park, Minnesota, Forenede Stater, 55416
        • Rekruttering
        • Park Nicollet Clinic - Saint Louis Park
        • Kontakt:
        • Ledende efterforsker:
          • David M. King
      • Saint Paul, Minnesota, Forenede Stater, 55101
        • Rekruttering
        • Regions Hospital
        • Kontakt:
        • Ledende efterforsker:
          • David M. King
      • Saint Paul, Minnesota, Forenede Stater, 55102
        • Rekruttering
        • United Hospital
        • Kontakt:
        • Ledende efterforsker:
          • David M. King
      • Virginia, Minnesota, Forenede Stater, 55792
        • Rekruttering
        • Essentia Health Virginia Clinic
        • Kontakt:
        • Ledende efterforsker:
          • Bret E. Friday
    • Mississippi
      • Columbus, Mississippi, Forenede Stater, 39705
        • Rekruttering
        • Baptist Memorial Hospital and Cancer Center-Golden Triangle
        • Ledende efterforsker:
          • Salil Goorha
        • Kontakt:
      • Grenada, Mississippi, Forenede Stater, 38901
        • Rekruttering
        • Baptist Cancer Center-Grenada
        • Ledende efterforsker:
          • Salil Goorha
        • Kontakt:
      • New Albany, Mississippi, Forenede Stater, 38652
        • Rekruttering
        • Baptist Memorial Hospital and Cancer Center-Union County
        • Ledende efterforsker:
          • Salil Goorha
        • Kontakt:
      • Oxford, Mississippi, Forenede Stater, 38655
        • Rekruttering
        • Baptist Memorial Hospital and Cancer Center-Oxford
        • Ledende efterforsker:
          • Salil Goorha
        • Kontakt:
      • Southhaven, Mississippi, Forenede Stater, 38671
        • Rekruttering
        • Baptist Memorial Hospital and Cancer Center-Desoto
        • Ledende efterforsker:
          • Salil Goorha
        • Kontakt:
    • Missouri
      • City of Saint Peters, Missouri, Forenede Stater, 63376
        • Rekruttering
        • Siteman Cancer Center at Saint Peters Hospital
        • Ledende efterforsker:
          • Geoffrey L. Uy
        • Kontakt:
      • Creve Coeur, Missouri, Forenede Stater, 63141
        • Rekruttering
        • Siteman Cancer Center at West County Hospital
        • Ledende efterforsker:
          • Geoffrey L. Uy
        • Kontakt:
      • Farmington, Missouri, Forenede Stater, 63640
        • Rekruttering
        • Parkland Health Center - Farmington
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 314-996-5569
      • Kansas City, Missouri, Forenede Stater, 64154
        • Rekruttering
        • University of Kansas Cancer Center - North
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Kansas City, Missouri, Forenede Stater, 64108
        • Rekruttering
        • University Health Truman Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 816-404-4375
        • Ledende efterforsker:
          • Tara L. Lin
      • Kansas City, Missouri, Forenede Stater, 64116
        • Rekruttering
        • University of Kansas Cancer Center - Briarcliff
        • Ledende efterforsker:
          • Tara L. Lin
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 913-588-3671
      • Lee's Summit, Missouri, Forenede Stater, 64064
        • Rekruttering
        • University of Kansas Cancer Center - Lee's Summit
        • Kontakt:
        • Ledende efterforsker:
          • Tara L. Lin
      • Saint Joseph, Missouri, Forenede Stater, 64506
        • Suspenderet
        • Heartland Regional Medical Center
      • Sainte Genevieve, Missouri, Forenede Stater, 63670
        • Rekruttering
        • Sainte Genevieve County Memorial Hospital
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 314-996-5569
      • St Louis, Missouri, Forenede Stater, 63110
        • Rekruttering
        • Washington University School of Medicine
        • Ledende efterforsker:
          • Geoffrey L. Uy
        • Kontakt:
      • St Louis, Missouri, Forenede Stater, 63129
        • Rekruttering
        • Siteman Cancer Center-South County
        • Ledende efterforsker:
          • Geoffrey L. Uy
        • Kontakt:
      • St Louis, Missouri, Forenede Stater, 63136
        • Rekruttering
        • Siteman Cancer Center at Christian Hospital
        • Ledende efterforsker:
          • Geoffrey L. Uy
        • Kontakt:
      • St Louis, Missouri, Forenede Stater, 63131
        • Rekruttering
        • Missouri Baptist Medical Center
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 314-996-5569
      • St Louis, Missouri, Forenede Stater, 63128
        • Suspenderet
        • Mercy Hospital South
      • Sullivan, Missouri, Forenede Stater, 63080
        • Rekruttering
        • Missouri Baptist Sullivan Hospital
        • Ledende efterforsker:
          • Bryan A. Faller
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 314-996-5569
    • Montana
      • Anaconda, Montana, Forenede Stater, 59711
        • Rekruttering
        • Community Hospital of Anaconda
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
      • Billings, Montana, Forenede Stater, 59101
        • Rekruttering
        • Billings Clinic Cancer Center
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
      • Bozeman, Montana, Forenede Stater, 59715
        • Rekruttering
        • Bozeman Health Deaconess Hospital
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
      • Great Falls, Montana, Forenede Stater, 59405
        • Rekruttering
        • Benefis Sletten Cancer Institute
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
      • Kalispell, Montana, Forenede Stater, 59901
        • Rekruttering
        • Logan Health Medical Center
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
      • Missoula, Montana, Forenede Stater, 59802
        • Rekruttering
        • Saint Patrick Hospital - Community Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Missoula, Montana, Forenede Stater, 59804
        • Rekruttering
        • Community Medical Center
        • Ledende efterforsker:
          • John M. Schallenkamp
        • Kontakt:
    • Nebraska
      • Bellevue, Nebraska, Forenede Stater, 68123
        • Rekruttering
        • Nebraska Medicine-Bellevue
        • Kontakt:
        • Ledende efterforsker:
          • Michael Haddadin
      • Omaha, Nebraska, Forenede Stater, 68198
        • Rekruttering
        • University of Nebraska Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Michael Haddadin
      • Omaha, Nebraska, Forenede Stater, 68118
        • Rekruttering
        • Nebraska Medicine-Village Pointe
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 402-559-5600
        • Ledende efterforsker:
          • Michael Haddadin
    • Nevada
      • Las Vegas, Nevada, Forenede Stater, 89102
        • Suspenderet
        • OptumCare Cancer Care at Charleston
      • Las Vegas, Nevada, Forenede Stater, 89183
        • Suspenderet
        • OptumCare Cancer Care at Fort Apache
      • Reno, Nevada, Forenede Stater, 89502
        • Suspenderet
        • Renown Regional Medical Center
    • New Hampshire
      • Lebanon, New Hampshire, Forenede Stater, 03756
        • Rekruttering
        • Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Raphael A. Lizcano
    • New Jersey
      • Basking Ridge, New Jersey, Forenede Stater, 07920
        • Rekruttering
        • Memorial Sloan Kettering Basking Ridge
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 212-639-7592
        • Ledende efterforsker:
          • Aaron D. Goldberg
      • Camden, New Jersey, Forenede Stater, 08103
        • Rekruttering
        • Cooper Hospital University Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 856-325-6757
        • Ledende efterforsker:
          • Michael Brister
      • Livingston, New Jersey, Forenede Stater, 07039
        • Rekruttering
        • Cooperman Barnabas Medical Center
        • Ledende efterforsker:
          • Neil D. Palmisiano
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 973-322-5200
      • Long Branch, New Jersey, Forenede Stater, 07740
        • Rekruttering
        • Monmouth Medical Center
        • Ledende efterforsker:
          • Neil D. Palmisiano
        • Kontakt:
      • Middletown, New Jersey, Forenede Stater, 07748
        • Rekruttering
        • Memorial Sloan Kettering Monmouth
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 212-639-7592
        • Ledende efterforsker:
          • Aaron D. Goldberg
      • Montvale, New Jersey, Forenede Stater, 07645
        • Rekruttering
        • Memorial Sloan Kettering Bergen
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 212-639-7592
        • Ledende efterforsker:
          • Aaron D. Goldberg
      • New Brunswick, New Jersey, Forenede Stater, 08903
        • Rekruttering
        • Rutgers Cancer Institute of New Jersey
        • Ledende efterforsker:
          • Neil D. Palmisiano
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 732-235-7356
      • Paramus, New Jersey, Forenede Stater, 07652
      • Ridgewood, New Jersey, Forenede Stater, 07450
      • Toms River, New Jersey, Forenede Stater, 08755
        • Rekruttering
        • Community Medical Center
        • Ledende efterforsker:
          • Neil D. Palmisiano
        • Kontakt:
    • New Mexico
      • Albuquerque, New Mexico, Forenede Stater, 87106
        • Rekruttering
        • University of New Mexico Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Charles Foucar
    • New York
      • Buffalo, New York, Forenede Stater, 14263
        • Rekruttering
        • Roswell Park Cancer Institute
        • Ledende efterforsker:
          • Eunice S. Wang
        • Kontakt:
      • Commack, New York, Forenede Stater, 11725
        • Rekruttering
        • Memorial Sloan Kettering Commack
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 212-639-7592
        • Ledende efterforsker:
          • Aaron D. Goldberg
      • Lake Success, New York, Forenede Stater, 11042
        • Rekruttering
        • Northwell Health/Center for Advanced Medicine
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 516-734-8896
        • Ledende efterforsker:
          • David Chitty
      • Manhasset, New York, Forenede Stater, 11030
        • Rekruttering
        • North Shore University Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 516-734-8896
        • Ledende efterforsker:
          • David Chitty
      • New York, New York, Forenede Stater, 10065
        • Rekruttering
        • Memorial Sloan Kettering Cancer Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 212-639-7592
        • Ledende efterforsker:
          • Aaron D. Goldberg
      • New York, New York, Forenede Stater, 10029
        • Rekruttering
        • Mount Sinai Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 212-824-7309
          • E-mail: CCTO@mssm.edu
        • Ledende efterforsker:
          • Douglas A. Tremblay
      • Rochester, New York, Forenede Stater, 14642
        • Rekruttering
        • University of Rochester
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 585-275-5830
        • Ledende efterforsker:
          • Jane L. Liesveld
      • Rochester, New York, Forenede Stater, 14621
        • Rekruttering
        • Rochester General Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Maria M. Sbenghe
      • Stony Brook, New York, Forenede Stater, 11794
        • Rekruttering
        • Stony Brook University Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 800-862-2215
        • Ledende efterforsker:
          • Suhu Liu
      • Syracuse, New York, Forenede Stater, 13210
        • Rekruttering
        • State University of New York Upstate Medical University
        • Ledende efterforsker:
          • Teresa C. Gentile
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 315-464-5476
      • The Bronx, New York, Forenede Stater, 10467
        • Rekruttering
        • Montefiore Medical Center - Moses Campus
        • Ledende efterforsker:
          • Ioannis Mantzaris
        • Kontakt:
      • Uniondale, New York, Forenede Stater, 11553
        • Rekruttering
        • Memorial Sloan Kettering Nassau
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 212-639-7592
        • Ledende efterforsker:
          • Aaron D. Goldberg
    • North Carolina
      • Chapel Hill, North Carolina, Forenede Stater, 27599
        • Rekruttering
        • UNC Lineberger Comprehensive Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Lacey S. Williams
      • Charlotte, North Carolina, Forenede Stater, 28203
        • Rekruttering
        • Carolinas Medical Center/Levine Cancer Institute
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 800-804-9376
        • Ledende efterforsker:
          • Brittany K. Ragon
      • Charlotte, North Carolina, Forenede Stater, 28204
        • Rekruttering
        • Novant Health Presbyterian Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Patricia L. Kropf
      • Durham, North Carolina, Forenede Stater, 27710
        • Rekruttering
        • Duke University Medical Center
        • Ledende efterforsker:
          • Harry P. Erba
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 888-275-3853
      • Greenville, North Carolina, Forenede Stater, 27834
        • Rekruttering
        • East Carolina University
        • Ledende efterforsker:
          • Darla K. Liles
        • Kontakt:
      • Wilmington, North Carolina, Forenede Stater, 28401
        • Rekruttering
        • Novant Health New Hanover Regional Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 910-342-3000
        • Ledende efterforsker:
          • Swaleh A. Bahamadi
      • Winston-Salem, North Carolina, Forenede Stater, 27157
        • Rekruttering
        • Wake Forest University Health Sciences
        • Ledende efterforsker:
          • Matthew J. Wieduwilt
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 336-713-6771
      • Winston-Salem, North Carolina, Forenede Stater, 27103
        • Rekruttering
        • Novant Health Forsyth Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • James P. Dugan
    • North Dakota
      • Bismarck, North Dakota, Forenede Stater, 58501
      • Fargo, North Dakota, Forenede Stater, 58122
      • Fargo, North Dakota, Forenede Stater, 58122
    • Ohio
      • Cleveland, Ohio, Forenede Stater, 44106
        • Rekruttering
        • Case Western Reserve University
        • Kontakt:
        • Ledende efterforsker:
          • Benjamin K. Tomlinson
      • Columbus, Ohio, Forenede Stater, 43210
        • Rekruttering
        • Ohio State University Comprehensive Cancer Center
        • Ledende efterforsker:
          • Alice S. Mims
        • Kontakt:
    • Oklahoma
      • Oklahoma City, Oklahoma, Forenede Stater, 73104
        • Rekruttering
        • University of Oklahoma Health Sciences Center
        • Kontakt:
        • Ledende efterforsker:
          • Manu Pandey
    • Oregon
      • Newberg, Oregon, Forenede Stater, 97132
        • Rekruttering
        • Providence Newberg Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Ontario, Oregon, Forenede Stater, 97914
        • Rekruttering
        • Saint Alphonsus Cancer Care Center-Ontario
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Oregon City, Oregon, Forenede Stater, 97045
        • Rekruttering
        • Providence Willamette Falls Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Portland, Oregon, Forenede Stater, 97213
        • Rekruttering
        • Providence Portland Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Portland, Oregon, Forenede Stater, 97225
        • Rekruttering
        • Providence Saint Vincent Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Charles W. Drescher
      • Portland, Oregon, Forenede Stater, 97239
        • Suspenderet
        • Oregon Health and Science University
    • Pennsylvania
      • Allentown, Pennsylvania, Forenede Stater, 18103
        • Rekruttering
        • Lehigh Valley Hospital-Cedar Crest
        • Kontakt:
        • Ledende efterforsker:
          • Tareq Al baghdadi
      • Danville, Pennsylvania, Forenede Stater, 17822
        • Rekruttering
        • Geisinger Medical Center
        • Ledende efterforsker:
          • Joseph J. Vadakara
        • Kontakt:
      • Hershey, Pennsylvania, Forenede Stater, 17033-0850
        • Rekruttering
        • Penn State Milton S Hershey Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Joseph Cioccio
      • Lewistown, Pennsylvania, Forenede Stater, 17044
        • Rekruttering
        • Lewistown Hospital
        • Ledende efterforsker:
          • Joseph J. Vadakara
        • Kontakt:
      • Philadelphia, Pennsylvania, Forenede Stater, 19107
        • Rekruttering
        • Thomas Jefferson University Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Margaret T. Kasner
      • Philadelphia, Pennsylvania, Forenede Stater, 19104
        • Rekruttering
        • University of Pennsylvania/Abramson Cancer Center
        • Ledende efterforsker:
          • Keith W. Pratz
        • Kontakt:
      • Pittsburgh, Pennsylvania, Forenede Stater, 15232
        • Rekruttering
        • UPMC Hillman Cancer Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 412-647-8073
        • Ledende efterforsker:
          • Annie P. Im
      • West Reading, Pennsylvania, Forenede Stater, 19611
        • Rekruttering
        • Reading Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 610-988-9323
        • Ledende efterforsker:
          • Terrence P. Cescon
      • Wilkes-Barre, Pennsylvania, Forenede Stater, 18711
        • Rekruttering
        • Geisinger Wyoming Valley/Henry Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Joseph J. Vadakara
    • Rhode Island
      • Providence, Rhode Island, Forenede Stater, 02903
        • Rekruttering
        • Rhode Island Hospital
        • Ledende efterforsker:
          • John L. Reagan
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 401-444-1488
    • South Carolina
      • Boiling Springs, South Carolina, Forenede Stater, 29316
        • Rekruttering
        • Prisma Health Cancer Institute - Spartanburg
        • Ledende efterforsker:
          • Suzanne R. Fanning
        • Kontakt:
      • Charleston, South Carolina, Forenede Stater, 29425
        • Rekruttering
        • Medical University of South Carolina
        • Ledende efterforsker:
          • Praneeth Baratam
        • Kontakt:
      • Easley, South Carolina, Forenede Stater, 29640
        • Rekruttering
        • Prisma Health Cancer Institute - Easley
        • Ledende efterforsker:
          • Suzanne R. Fanning
        • Kontakt:
      • Greenville, South Carolina, Forenede Stater, 29605
        • Rekruttering
        • Prisma Health Cancer Institute - Faris
        • Ledende efterforsker:
          • Suzanne R. Fanning
        • Kontakt:
      • Greenville, South Carolina, Forenede Stater, 29605
        • Rekruttering
        • Prisma Health Cancer Institute - Butternut
        • Ledende efterforsker:
          • Suzanne R. Fanning
        • Kontakt:
      • Greenville, South Carolina, Forenede Stater, 29615
        • Rekruttering
        • Prisma Health Cancer Institute - Eastside
        • Ledende efterforsker:
          • Suzanne R. Fanning
        • Kontakt:
      • Greer, South Carolina, Forenede Stater, 29650
        • Rekruttering
        • Prisma Health Cancer Institute - Greer
        • Ledende efterforsker:
          • Suzanne R. Fanning
        • Kontakt:
      • Seneca, South Carolina, Forenede Stater, 29672
        • Rekruttering
        • Prisma Health Cancer Institute - Seneca
        • Ledende efterforsker:
          • Suzanne R. Fanning
        • Kontakt:
    • South Dakota
      • Sioux Falls, South Dakota, Forenede Stater, 57104
      • Sioux Falls, South Dakota, Forenede Stater, 57117-5134
    • Tennessee
      • Collierville, Tennessee, Forenede Stater, 38017
        • Rekruttering
        • Baptist Memorial Hospital and Cancer Center-Collierville
        • Ledende efterforsker:
          • Salil Goorha
        • Kontakt:
      • Knoxville, Tennessee, Forenede Stater, 37920
        • Suspenderet
        • University of Tennessee - Knoxville
      • Memphis, Tennessee, Forenede Stater, 38120
        • Rekruttering
        • Baptist Memorial Hospital and Cancer Center-Memphis
        • Ledende efterforsker:
          • Salil Goorha
        • Kontakt:
    • Texas
      • Houston, Texas, Forenede Stater, 77030
        • Rekruttering
        • Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 713-798-1354
          • E-mail: burton@bcm.edu
        • Ledende efterforsker:
          • Tareq Abuasab
      • Houston, Texas, Forenede Stater, 77030
        • Rekruttering
        • Ben Taub General Hospital
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 713-873-2000
        • Ledende efterforsker:
          • Tareq Abuasab
    • Utah
      • Salt Lake City, Utah, Forenede Stater, 84112
        • Rekruttering
        • Huntsman Cancer Institute/University of Utah
        • Kontakt:
        • Ledende efterforsker:
          • Paul J. Shami
      • Salt Lake City, Utah, Forenede Stater, 84148
        • Rekruttering
        • George E Wahlen Department of Veterans Affairs Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 801-582-1565
        • Ledende efterforsker:
          • Tsewang Tashi
    • Vermont
      • Burlington, Vermont, Forenede Stater, 05401
        • Rekruttering
        • University of Vermont Medical Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 802-656-4101
          • E-mail: rpo@uvm.edu
        • Ledende efterforsker:
          • Diego A. Adrianzen Herrera
      • Burlington, Vermont, Forenede Stater, 05405
        • Rekruttering
        • University of Vermont and State Agricultural College
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 802-656-8990
          • E-mail: rpo@uvm.edu
        • Ledende efterforsker:
          • Diego A. Adrianzen Herrera
    • Virginia
      • Charlottesville, Virginia, Forenede Stater, 22908
      • Fairfax, Virginia, Forenede Stater, 22031
        • Rekruttering
        • Inova Schar Cancer Institute
        • Kontakt:
        • Ledende efterforsker:
          • Danielle A. Shafer
      • Falls Church, Virginia, Forenede Stater, 22042
        • Rekruttering
        • Inova Fairfax Hospital
        • Kontakt:
        • Ledende efterforsker:
          • Danielle A. Shafer
      • Richmond, Virginia, Forenede Stater, 23298
        • Rekruttering
        • VCU Massey Comprehensive Cancer Center
        • Ledende efterforsker:
          • Keri R. Maher
        • Kontakt:
    • Washington
      • Edmonds, Washington, Forenede Stater, 98026
        • Rekruttering
        • Swedish Cancer Institute-Edmonds
        • Ledende efterforsker:
          • Charles W. Drescher
        • Kontakt:
      • Issaquah, Washington, Forenede Stater, 98029
        • Rekruttering
        • Swedish Cancer Institute-Issaquah
        • Ledende efterforsker:
          • Charles W. Drescher
        • Kontakt:
      • Seattle, Washington, Forenede Stater, 98122
        • Rekruttering
        • Swedish Medical Center-First Hill
        • Ledende efterforsker:
          • Charles W. Drescher
        • Kontakt:
      • Seattle, Washington, Forenede Stater, 98195
        • Rekruttering
        • University of Washington Medical Center - Montlake
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 800-804-8824
        • Ledende efterforsker:
          • Jacob S. Appelbaum
      • Seattle, Washington, Forenede Stater, 98109
        • Rekruttering
        • Fred Hutchinson Cancer Center
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 800-804-8824
        • Ledende efterforsker:
          • Jacob S. Appelbaum
    • Wisconsin
      • Appleton, Wisconsin, Forenede Stater, 54911
        • Rekruttering
        • ThedaCare Regional Cancer Center
        • Kontakt:
        • Ledende efterforsker:
          • Yazhini Vallatharasu
      • Ashland, Wisconsin, Forenede Stater, 54806
        • Rekruttering
        • Duluth Clinic Ashland
        • Kontakt:
        • Ledende efterforsker:
          • Bret E. Friday
      • Burlington, Wisconsin, Forenede Stater, 53105
        • Rekruttering
        • Aurora Cancer Care-Southern Lakes VLCC
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Cudahy, Wisconsin, Forenede Stater, 53110
        • Rekruttering
        • Aurora Saint Luke's South Shore
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Eau Claire, Wisconsin, Forenede Stater, 54701
      • Germantown, Wisconsin, Forenede Stater, 53022
        • Rekruttering
        • Aurora Health Care Germantown Health Center
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Grafton, Wisconsin, Forenede Stater, 53024
        • Rekruttering
        • Aurora Cancer Care-Grafton
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Green Bay, Wisconsin, Forenede Stater, 54311
        • Rekruttering
        • Aurora BayCare Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Green Bay, Wisconsin, Forenede Stater, 54301
        • Rekruttering
        • Saint Vincent Hospital Cancer Center Green Bay
        • Ledende efterforsker:
          • Matthew L. Ryan
        • Kontakt:
      • Green Bay, Wisconsin, Forenede Stater, 54303
        • Rekruttering
        • Saint Vincent Hospital Cancer Center at Saint Mary's
        • Ledende efterforsker:
          • Matthew L. Ryan
        • Kontakt:
      • Janesville, Wisconsin, Forenede Stater, 53548
        • Rekruttering
        • Mercyhealth Hospital and Cancer Center - Janesville
        • Kontakt:
        • Ledende efterforsker:
          • Emily G. Robinson
      • Kenosha, Wisconsin, Forenede Stater, 53142
        • Rekruttering
        • Aurora Cancer Care-Kenosha South
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • La Crosse, Wisconsin, Forenede Stater, 54601
        • Rekruttering
        • Gundersen Lutheran Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • David E. Marinier
      • Madison, Wisconsin, Forenede Stater, 53705
        • Rekruttering
        • William S Middleton VA Medical Center
        • Ledende efterforsker:
          • Christopher D. Fletcher
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 17007 608-256-1901
      • Madison, Wisconsin, Forenede Stater, 53792
        • Rekruttering
        • University of Wisconsin Carbone Cancer Center - University Hospital
        • Ledende efterforsker:
          • Kieran D. Sahasrabudhe
        • Kontakt:
      • Madison, Wisconsin, Forenede Stater, 53718
        • Rekruttering
        • University of Wisconsin Carbone Cancer Center - Eastpark Medical Center
        • Ledende efterforsker:
          • Kieran D. Sahasrabudhe
        • Kontakt:
      • Marinette, Wisconsin, Forenede Stater, 54143
        • Rekruttering
        • Aurora Bay Area Medical Group-Marinette
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Marshfield, Wisconsin, Forenede Stater, 54449
      • Menomonee Falls, Wisconsin, Forenede Stater, 53051
        • Rekruttering
        • Froedtert Menomonee Falls Hospital
        • Ledende efterforsker:
          • Ehab L. Atallah
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 262-257-5100
      • Milwaukee, Wisconsin, Forenede Stater, 53209
        • Rekruttering
        • Aurora Cancer Care-Milwaukee
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Milwaukee, Wisconsin, Forenede Stater, 53215
        • Rekruttering
        • Aurora Saint Luke's Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Milwaukee, Wisconsin, Forenede Stater, 53226
        • Rekruttering
        • Medical College of Wisconsin
        • Ledende efterforsker:
          • Ehab L. Atallah
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 414-805-3666
      • Milwaukee, Wisconsin, Forenede Stater, 53233
        • Rekruttering
        • Aurora Sinai Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Minocqua, Wisconsin, Forenede Stater, 54548
      • Mukwonago, Wisconsin, Forenede Stater, 53149
        • Rekruttering
        • ProHealth D N Greenwald Center
        • Kontakt:
        • Ledende efterforsker:
          • Timothy R. Wassenaar
      • New Berlin, Wisconsin, Forenede Stater, 53151
        • Rekruttering
        • Froedtert and MCW Moorland Reserve Health Center
        • Ledende efterforsker:
          • Ehab L. Atallah
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 414-805-0505
      • Oak Creek, Wisconsin, Forenede Stater, 53154
        • Rekruttering
        • Drexel Town Square Health Center
        • Ledende efterforsker:
          • Ehab L. Atallah
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 414-805-0505
      • Oconomowoc, Wisconsin, Forenede Stater, 53066
        • Rekruttering
        • ProHealth Oconomowoc Memorial Hospital
        • Ledende efterforsker:
          • Timothy R. Wassenaar
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 262-928-7878
      • Oconto Falls, Wisconsin, Forenede Stater, 54154
        • Rekruttering
        • Saint Vincent Hospital Cancer Center at Oconto Falls
        • Ledende efterforsker:
          • Matthew L. Ryan
        • Kontakt:
      • Oshkosh, Wisconsin, Forenede Stater, 54904
        • Rekruttering
        • Vince Lombardi Cancer Clinic - Oshkosh
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Racine, Wisconsin, Forenede Stater, 53406
        • Rekruttering
        • Aurora Cancer Care-Racine
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Rice Lake, Wisconsin, Forenede Stater, 54868
      • Sheboygan, Wisconsin, Forenede Stater, 53081
        • Rekruttering
        • Vince Lombardi Cancer Clinic-Sheboygan
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Sheboygan, Wisconsin, Forenede Stater, 53081
        • Rekruttering
        • Saint Vincent Hospital Cancer Center at Sheboygan
        • Ledende efterforsker:
          • Matthew L. Ryan
        • Kontakt:
      • Stevens Point, Wisconsin, Forenede Stater, 54482
      • Sturgeon Bay, Wisconsin, Forenede Stater, 54235-1495
        • Rekruttering
        • Saint Vincent Hospital Cancer Center at Sturgeon Bay
        • Ledende efterforsker:
          • Matthew L. Ryan
        • Kontakt:
      • Summit, Wisconsin, Forenede Stater, 53066
        • Rekruttering
        • Aurora Medical Center in Summit
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Two Rivers, Wisconsin, Forenede Stater, 54241
        • Rekruttering
        • Vince Lombardi Cancer Clinic-Two Rivers
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • Waukesha, Wisconsin, Forenede Stater, 53188
        • Rekruttering
        • ProHealth Waukesha Memorial Hospital
        • Ledende efterforsker:
          • Timothy R. Wassenaar
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 262-928-7632
      • Waukesha, Wisconsin, Forenede Stater, 53188
        • Rekruttering
        • UW Cancer Center at ProHealth Care
        • Ledende efterforsker:
          • Timothy R. Wassenaar
        • Kontakt:
      • Wauwatosa, Wisconsin, Forenede Stater, 53226
        • Rekruttering
        • Aurora Cancer Care-Milwaukee West
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • West Allis, Wisconsin, Forenede Stater, 53227
        • Rekruttering
        • Aurora West Allis Medical Center
        • Kontakt:
        • Ledende efterforsker:
          • Thomas J. Saphner
      • West Bend, Wisconsin, Forenede Stater, 53095
        • Rekruttering
        • Froedtert West Bend Hospital/Kraemer Cancer Center
        • Ledende efterforsker:
          • Ehab L. Atallah
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 414-805-0505
      • Weston, Wisconsin, Forenede Stater, 54476
  • Puerto Rico
      • San Juan, Puerto Rico, 00927
        • Rekruttering
        • Centro Comprensivo de Cancer de UPR
        • Ledende efterforsker:
          • Luis J. Santos Reyes
        • Kontakt:
      • San Juan, Puerto Rico, 00936
        • Rekruttering
        • San Juan City Hospital
        • Ledende efterforsker:
          • Luis J. Santos Reyes
        • Kontakt:
          • Site Public Contact
          • Telefonnummer: 787-763-1296

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Participants must be suspected to have previously untreated acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). Participants with AML cannot have a history of previously treated myeloproliferative neoplasms (MPN) or MDS.

  • Participants must be >= 18 years of age.

  • Participants must not have received prior anti-cancer therapy for AML or MDS.

    • Note: Hydroxyurea to control the white blood cell count (WBC) is allowed.
    • Note: Prior erythroid stimulating agent (ESA) is not considered prior therapy for the purposes of eligibility. Participants must not be currently receiving any cytarabine-containing therapy other than up to 1 g/m^2 of cytarabine, which is allowed for urgent cytoreduction.

  • Participants are allowed prior use of hydroxyurea, all-trans retinoic acid (ATRA), BCR-ABL directed tyrosine kinase inhibitor, erythropoiesis-stimulating agent, thrombopoietin receptor agonist and lenalidomide, with a maximum limit of 1 month of exposure.

    • Note: Participants receiving hydroxyurea prior to treatment substudy or TAP assignment must agree to discontinue hydroxyurea within 24 hours before beginning substudy or TAP treatment.

  • Participants must not have a prior or concurrent malignancy that requires concurrent anti-cancer therapy

    • Note: active hormonal therapy is allowed

  • Participants must have a Zubrod Performance Status evaluation within 28 days prior to registration.

  • Participants must agree to have translational medicine specimens submitted.

  • Participants must be offered the opportunity to participate in specimen banking.

    • Note: Specimens must be collected and submitted following the initial paper-based process and subsequently via the Precision Medicine Specimen Tracking Forms in Medidata Rave instance for the MyeloMATCH MSRP.

  • Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines.

    • Note: As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system.

  • The master screening and reassessment protocol (MSRP) should only be used in sites where the relevant AML treatment substudies are open or if the site is willing to follow the MSRP Tier Advancement Pathway (TAP) for patients in the event that the site does not have the relevant study open and transfer to another site that does have the study open. For example, if a site does not have a myeloMATCH Tier 1 study for older AML open for enrollment, such older AML patients should only be consented for the MSRP if the site is willing to treat the patient with standard of care on TAP or is willing to transfer the patient to a center with a study open that the patient would otherwise match to.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Screening
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: MM1MDS-A01 Regimen 1 (ASTX727)

Patients receive ASTX727 PO QD on days 1-5 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients who do not achieve a CR, CRL, or CRh at the end of cycle 6 may cross-over to Regimen 2. Patients who experience CR, PR, or SD any time after 4 cycles of treatment may be reassessed in order to go to a higher myeloMATCH tier assignment or to TAP. Patients also undergo bone marrow biopsy and aspiration throughout the study. Patients may also undergo optional buccal swab on study, and/or optional additional bone marrow aspiration and blood sample collection on study and at disease progression.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1MDS-A01 Regimen 2 (ASTX727, enasidenib)

Patients receive ASTX727 PO QD on days 1-5 and enasidenib PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients who experience CR, PR, or SD any time after 4 cycles of treatment may be reassessed in order to go to a higher myeloMATCH tier assignment or to TAP. Patients also undergo bone marrow biopsy and aspiration throughout the study. Patients may also undergo optional buccal swab on study, and/or optional additional bone marrow aspiration and blood sample collection on study and at disease progression.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Enasidenib

Given PO

Andre navne:
  • AG-221
  • CC-90007 fri base
  • AG 221
  • AG221
Eksperimentel: MM1MDS-CTG02 Arm 1 (Luspatercept)

Patients receive luspatercept SC on day 1 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Biologisk: Luspatercept

Given SC

Andre navne:
  • ACE-536
  • Luspatercept-aamt
  • Reblozyl
  • ACE 536
  • ACE536
Eksperimentel: MM1MDS-CTG02 Arm 2 (Luspatercept with epoetin alfa)

Patients receive luspatercept SC on day 1 and epoetin alfa SC QW for each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.
Biologisk: Epoetin Alfa

Given SC

Andre navne:
  • Epogen
  • EPO
  • Procrit
  • Eprex
  • Epoetin alfa-epbx
  • Retacrit
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Biologisk: Luspatercept

Given SC

Andre navne:
  • ACE-536
  • Luspatercept-aamt
  • Reblozyl
  • ACE 536
  • ACE536
Eksperimentel: MM1MDS-CTG02 Arm 3 (Luspatercept and emavusertib)

Patients receive luspatercept SC on day 1 and emavusertib PO BID on days 1-21 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Biologisk: Luspatercept

Given SC

Andre navne:
  • ACE-536
  • Luspatercept-aamt
  • Reblozyl
  • ACE 536
  • ACE536
Biologisk: Emavusertib

Given PO

Andre navne:
  • CA-4948
  • AU 4948
  • AU-4948
  • CA 4948
  • CA4948
  • Interleukin-1-receptor-associeret kinase 4-inhibitor CA-4948
  • IRAK4-hæmmer CA-4948
Eksperimentel: MM1OA-EA02 Regimen 1 (azacitidine, venetoclax)

INDUCTION: Patients receive azacitidine IV or SC on days 1-7 of each cycle and venetoclax PO on days 1-28 of each cycle. Treatment repeats every 28 days for up to 2 cycles or until bone marrow assessment shows at least an MLFS response or better ("better" defined as CR, CRi, CRh), in the absence of disease progression or unacceptable toxicity.

CONSOLIDATION: Patients receive azacitidine IV or SC on days 1-7 and venetoclax PO on days 1-28 of each cycle. Cycles repeat every 28 days for 2 years in the absence of disease progression or unacceptable toxicity.

Patients undergo bone marrow biopsy and aspiration as well as blood sample collection on the trial.
Procedure: Biopsy Procedure

Undergo biopsy

Andre navne:
  • Bx
  • BIOPSY_TYPE
  • Biopsi
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Azacitidine

Given IV or SC

Andre navne:
  • 5 AZC
  • 5-AC
  • 5-Azacytidin
  • 5-AZC
  • Azacytidin
  • Azacytidin, 5-
  • Ladakamycin
  • Mylosar
  • U-18496
  • Vidaza
  • 5-azacitidin
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1OA-EA02 Regimen 2 (azacitidine, venetoclax, gilteritinib)

INDUCTION: Patients receive azacitidine IV or SC on days 1-7 and venetoclax and gilteritinib PO on days 1-28 of each cycle. Treatment repeats every 28 days for up to 2 cycles or until bone marrow assessment shows at least an MLFS response or better ("better" defined as CR, CRi, CRh), in the absence of disease progression or unacceptable toxicity.

CONSOLIDATION: Patients receive azacitidine IV or SC on days 1-5, venetoclax PO on days 1-7 and gilteritinib PO on days 1-28 of each cycle. Cycles repeat every 28 days for 2 years in the absence of disease progression or unacceptable toxicity.

Patients undergo bone marrow biopsy and aspiration as well as blood sample collection on the trial.
Procedure: Biopsy Procedure

Undergo biopsy

Andre navne:
  • Bx
  • BIOPSY_TYPE
  • Biopsi
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Azacitidine

Given IV or SC

Andre navne:
  • 5 AZC
  • 5-AC
  • 5-Azacytidin
  • 5-AZC
  • Azacytidin
  • Azacytidin, 5-
  • Ladakamycin
  • Mylosar
  • U-18496
  • Vidaza
  • 5-azacitidin
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Gilteritinib

Given PO

Andre navne:
  • ASP2215
  • ASP-2215
  • ASP 2215
Eksperimentel: MM1OA-EA02 Regimen 3 (azacitidine, venetoclax, gilteritinib)

INDUCTION: Patients receive azacitidine IV or SC on days 1-7 and venetoclax PO on days 1-28, and gilteritinib PO on days 8-21 of each cycle. Treatment repeats every 28 days for up to 2 cycles or until bone marrow assessment shows at least an MLFS response or better ("better" defined as CR, CRi, CRh), in the absence of disease progression or unacceptable toxicity.

CONSOLIDATION: Patients receive azacitidine IV or SC on days 1-5, venetoclax PO on days 1-14 and gilteritinib PO on days 8-21 of each cycle. Cycles repeat every 28 days for 2 years in the absence of disease progression or unacceptable toxicity.

Patients undergo bone marrow biopsy and aspiration as well as blood sample collection on the trial.
Procedure: Biopsy Procedure

Undergo biopsy

Andre navne:
  • Bx
  • BIOPSY_TYPE
  • Biopsi
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Azacitidine

Given IV or SC

Andre navne:
  • 5 AZC
  • 5-AC
  • 5-Azacytidin
  • 5-AZC
  • Azacytidin
  • Azacytidin, 5-
  • Ladakamycin
  • Mylosar
  • U-18496
  • Vidaza
  • 5-azacitidin
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Gilteritinib

Given PO

Andre navne:
  • ASP2215
  • ASP-2215
  • ASP 2215
Aktiv komparator: MM1OA-MDS-A05 Cohort A, Arm 1 (ASTX727, venetoclax)

Patients receive ASTX727 PO QD on days 1-5 of each cycle and venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for 4 cycles in the absence of disease progression or unacceptable toxicity. Patients with CR, CRh, or CRi after cycle 4 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1OA-MDS-A05 Cohort A,Arm 2 (ASTX727,venetoclax,olutasidenib)

Patients receive ASTX727 PO QD on days 1-5 of each cycle, venetoclax PO QD on days 1-28 of each cycle, and olutasidenib PO BID on days 1-28 of each cycle. Cycles repeat every 28 days for 4 cycles in the absence of disease progression or unacceptable toxicity. Patients with CR, CRh, or CRi after cycle 4 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Olutasidenib

Given PO

Andre navne:
  • FT 2102
  • FT-2102
  • FT2102
  • IDH1-R132 Inhibitor FT-2102
  • Rezlidhia
Eksperimentel: MM1OA-MDS-A05 Cohort B, Arm 3 (ASTX727, olutasidenib)

Patients receive ASTX727 PO QD on days 1-5 of each cycle and olutasidenib PO BID on days 1-28 of each cycle. Cycles repeat every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients with CR continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Olutasidenib

Given PO

Andre navne:
  • FT 2102
  • FT-2102
  • FT2102
  • IDH1-R132 Inhibitor FT-2102
  • Rezlidhia
Aktiv komparator: MM1OA-MDS-A05 Cohort B, Arm 4 (ASTX727)

Patients receive ASTX727 PO QD on days 1-5 of each cycle. Cycles repeat every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients without CR after cycle 6 may then cross-over to Arm 3. Patients with CR, as well as patients without CR but deriving clinical benefit after cycle 6 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1OA-MDS-A05 Cohort C (olutasidenib)

Patients receive olutasidenib PO BID on days 1-28 of each cycle. Cycles repeat every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients deriving clinical benefit after cycle 6 continue treatment cycles every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow biopsy/aspiration and collection of blood samples throughout the trial.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Olutasidenib

Given PO

Andre navne:
  • FT 2102
  • FT-2102
  • FT2102
  • IDH1-R132 Inhibitor FT-2102
  • Rezlidhia
Aktiv komparator: MM1OA-S03 Arm 1 (ASTX727, venetoclax)

Patients receive ASTX727 PO QD on days 1-5 and venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo blood sample collection, bone marrow aspiration, and bone marrow biopsy throughout the trial.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1OA-S03 Arm 2 (ASTX727, venetoclax, enasidenib)

Patients receive ASTX727 PO QD on days 1-5, venetoclax PO QD on days 1-28, and enasidenib PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo blood sample collection, bone marrow aspiration, and bone marrow biopsy throughout the trial.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Enasidenib

Given PO

Andre navne:
  • AG-221
  • CC-90007 fri base
  • AG 221
  • AG221
Aktiv komparator: MM1OA-S04 Arm 1 (ASTX727 with standard duration venetoclax)

Patients receive ASTX727 PO QD on days 1-5 and venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1OA-S04 Arm 2 (ASTX727 with shorter duration venetoclax)

Patients receive ASTX727 PO QD on days 1-5 and venetoclax PO QD on days 1-14 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and blood sample collection throughout the study.
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Decitabine and Cedazuridine

Given PO

Andre navne:
  • ASTX727
  • CDA-hæmmer E7727/Decitabin-kombinationsmiddel ASTX727
  • Cedazuridin/Decitabin kombinationsmiddel ASTX727
  • Cedazuridin/Decitabine tablet
  • Inqovi
  • C-DEC
  • DEC-C
  • ASTX 727
  • ASTX-727
  • Inaqovi
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Aktiv komparator: MM1YA-A04 Regimen 1 (gemtuzumab ozogamicin, chemotherapy)

Patients receive gemtuzumab ozogamicin IV on day 1, 2 or 3 and on day 4, 5, or 6 (NOTE: two doses must be at least 3 days apart), as well as cytarabine IV, continuously, on days 1-7 and daunorubicin IV on days 1-3 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or MUGA scan during screening, as well as bone marrow aspiration and blood sample collection throughout the study.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Medicin: Gemtuzumab Ozogamicin

Given IV

Andre navne:
  • Mylotarg
  • Calicheamicin-konjugeret humaniseret anti-CD33 monoklonalt antistof
  • CDP-771
  • CMA-676
  • gemtuzumab
  • hP67.6-Calicheamicin
  • WAY-CMA-676
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Daunorubicin Hydrochloride

Given IV

Andre navne:
  • Cerubidin
  • Cloridrato de Daunorubicina
  • Daunoblastin
  • Daunoblastina
  • Daunomycin hydrochlorid
  • Daunomycin, hydrochlorid
  • Daunorubicin.HCl
  • Daunorubicini Hydrochloridum
  • FI-6339
  • Ondena
  • RP-13057
  • Rubidomycin hydrochlorid
  • Rubilem
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Andet: Best Practice

Receive SOC treatment

Andre navne:
  • plejestandard
  • standard terapi
Eksperimentel: MM1YA-A04 Regimen 2 (venetoclax, chemotherapy)

Patients receive venetoclax PO QD on days 1-11, cytarabine IV, continuously, on days 2-8 and daunorubicin IV on days 2-4 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or MUGA scan during screening and bone marrow aspiration, as well as blood sample collection throughout the study.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Daunorubicin Hydrochloride

Given IV

Andre navne:
  • Cerubidin
  • Cloridrato de Daunorubicina
  • Daunoblastin
  • Daunoblastina
  • Daunomycin hydrochlorid
  • Daunomycin, hydrochlorid
  • Daunorubicin.HCl
  • Daunorubicini Hydrochloridum
  • FI-6339
  • Ondena
  • RP-13057
  • Rubidomycin hydrochlorid
  • Rubilem
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Andet: Best Practice

Receive SOC treatment

Andre navne:
  • plejestandard
  • standard terapi
Eksperimentel: MM1YA-CTG01 Arm I (daunorubicin, cytarabine, venetoclax)

Patients receive daunorubicin IV on days 2-4, cytarabine IV continuously on days 2-8, and venetoclax PO QD on days 1-11. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Based on a bone marrow aspiration assessment (completed at the discretion of the treating investigator), patients may receive reinduction consisting of daunorubicin IV on days 2-3, cytarabine IV continuously on days 2-6, and venetoclax PO QD on days 1-8. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow aspiration and collection of blood samples on study and as clinically indicated. Additionally, patients undergo ECHO or MUGA during screening.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Daunorubicin Hydrochloride

Given IV

Andre navne:
  • Cerubidin
  • Cloridrato de Daunorubicina
  • Daunoblastin
  • Daunoblastina
  • Daunomycin hydrochlorid
  • Daunomycin, hydrochlorid
  • Daunorubicin.HCl
  • Daunorubicini Hydrochloridum
  • FI-6339
  • Ondena
  • RP-13057
  • Rubidomycin hydrochlorid
  • Rubilem
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1YA-CTG01 Arm II (azacitidine, venetoclax)

Patients receive azacitidine IV or SC on days 1-7 or days 1-5 and 8-9 and venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for a total of 2 cycles, in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow aspiration and collection of blood samples on study and as clinically indicated. Additionally, patients undergo ECHO or MUGA during screening.
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Azacitidine

Given IV or SC

Andre navne:
  • 5 AZC
  • 5-AC
  • 5-Azacytidin
  • 5-AZC
  • Azacytidin
  • Azacytidin, 5-
  • Ladakamycin
  • Mylosar
  • U-18496
  • Vidaza
  • 5-azacitidin
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Aktiv komparator: MM1YA-CTG01 Arm III (daunorubicin, cytarabine)

Patients receive daunorubicin IV on days 1-3 and cytarabine IV, continuously, on days 1-7. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Based on a bone marrow aspiration assessment (completed at the discretion of the treating investigator), patients may receive reinduction consisting of cytarabine IV, continuously, on days 1-5 and daunorubicin IV on days 1-2. Cycle is 28 days and treatment is given in the absence of disease progression or unacceptable toxicity. Patients also undergo bone marrow aspiration and collection of blood samples on study and as clinically indicated. Additionally, patients undergo ECHO or MUGA during screening.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Daunorubicin Hydrochloride

Given IV

Andre navne:
  • Cerubidin
  • Cloridrato de Daunorubicina
  • Daunoblastin
  • Daunoblastina
  • Daunomycin hydrochlorid
  • Daunomycin, hydrochlorid
  • Daunorubicin.HCl
  • Daunorubicini Hydrochloridum
  • FI-6339
  • Ondena
  • RP-13057
  • Rubidomycin hydrochlorid
  • Rubilem
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1YA-EA05 Arm A (cytarabine, daunorubicin, quizartinib)

See Detailed Description.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Daunorubicin

Given IV

Andre navne:
  • DNR
  • Rubidomycin
  • Daunomycin
  • Daunorrubicina
  • Leukaemomycin C
  • Rubomycin C
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Quizartinib

Given PO

Andre navne:
  • AC-220
  • AC010220
  • AC220
  • ASP2689
  • Vanflyta
  • AC 220
  • ASP 2689
  • ASP-2689
Eksperimentel: MM1YA-EA05 Arm B (azacitidine, venetoclax, quizartinib)

See Detailed Description.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Azacitidine

Given IV or SC

Andre navne:
  • 5 AZC
  • 5-AC
  • 5-Azacytidin
  • 5-AZC
  • Azacytidin
  • Azacytidin, 5-
  • Ladakamycin
  • Mylosar
  • U-18496
  • Vidaza
  • 5-azacitidin
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Medicin: Quizartinib

Given PO

Andre navne:
  • AC-220
  • AC010220
  • AC220
  • ASP2689
  • Vanflyta
  • AC 220
  • ASP 2689
  • ASP-2689
Aktiv komparator: MM1YA-S01 Arm I (cytarabine, daunorubicin)

Patients receive cytarabine IV continuously on days 1-7 and daunorubicin IV on days 1-3 per standard approach of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of cytarabine IV continuously on days 1-5 and daunorubicin IV on days 1-2. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Daunorubicin Hydrochloride

Given IV

Andre navne:
  • Cerubidin
  • Cloridrato de Daunorubicina
  • Daunoblastin
  • Daunoblastina
  • Daunomycin hydrochlorid
  • Daunomycin, hydrochlorid
  • Daunorubicin.HCl
  • Daunorubicini Hydrochloridum
  • FI-6339
  • Ondena
  • RP-13057
  • Rubidomycin hydrochlorid
  • Rubilem
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1YA-S01 Arm II (cytarabine, daunorubicin, venetoclax)

Patients receive cytarabine IV continuously on days 2-8 and daunorubicin IV on days 2-4 with venetoclax PO on days 1-11 of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of cytarabine IV continuously on days 2-6 and daunorubicin IV on days 2-3 with venetoclax PO on days 1-8. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Daunorubicin Hydrochloride

Given IV

Andre navne:
  • Cerubidin
  • Cloridrato de Daunorubicina
  • Daunoblastin
  • Daunoblastina
  • Daunomycin hydrochlorid
  • Daunomycin, hydrochlorid
  • Daunorubicin.HCl
  • Daunorubicini Hydrochloridum
  • FI-6339
  • Ondena
  • RP-13057
  • Rubidomycin hydrochlorid
  • Rubilem
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1YA-S01 Arm III (azacitidine, venetoclax)

Patients receive azacitidine SC or IV on days 1-7 and venetoclax PO on days 1-28 of each cycle. Cycles repeat every 28 days for 2 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Azacitidine

Given IV or SC

Andre navne:
  • 5 AZC
  • 5-AC
  • 5-Azacytidin
  • 5-AZC
  • Azacytidin
  • Azacytidin, 5-
  • Ladakamycin
  • Mylosar
  • U-18496
  • Vidaza
  • 5-azacitidin
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1YA-S01 Arm IV (Vyxeos)

Patients receive daunorubicin and cytarabine liposome IV over 90 minutes on days 1, 3, and 5 of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of daunorubicin and cytarabine liposome IV over 90 minutes on days 1 and 3. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Liposome-encapsulated Daunorubicin-Cytarabine

Given IV

Andre navne:
  • CPX-351
  • Cytarabin-Daunorubicin liposom til injektion
  • Daunorubicin og Cytarabin (liposomal)
  • Liposomal AraC-Daunorubicin CPX-351
  • Liposomal Cytarabin-Daunorubicin
  • Liposom-indkapslet kombination af Daunorubicin og Cytarabin
  • Vyxeos
  • Cytarabin og Daunorubicin Liposomal
  • CPX 351
  • CPX351
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: MM1YA-S01 Arm V (Vyxeos, venetoclax)

Patients receive daunorubicin and cytarabine liposome IV over 90 minutes on days 1, 3, and 5 and venetoclax PO on days 1-14 of each cycle. Cycles repeat every 28 days for 1 cycle in the absence of disease progression or unacceptable toxicity. Patients may receive an additional cycle of daunorubicin and cytarabine liposome IV over 90 minutes on days 1 and 3 and venetoclax PO on days 1-7. Patients undergo ECHO or MUGA scan during screening. Patients also undergo a bone marrow aspiration and collection of blood throughout the trial.
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Bone Marrow Aspiration

Undergo bone marrow aspiration

Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Liposome-encapsulated Daunorubicin-Cytarabine

Given IV

Andre navne:
  • CPX-351
  • Cytarabin-Daunorubicin liposom til injektion
  • Daunorubicin og Cytarabin (liposomal)
  • Liposomal AraC-Daunorubicin CPX-351
  • Liposomal Cytarabin-Daunorubicin
  • Liposom-indkapslet kombination af Daunorubicin og Cytarabin
  • Vyxeos
  • Cytarabin og Daunorubicin Liposomal
  • CPX 351
  • CPX351
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Aktiv komparator: MM2YA-EA01 Arm A (cytarabine)

Patients receive cytarabine IV on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Biopsy Procedure

Undergo biopsy

Andre navne:
  • Bx
  • BIOPSY_TYPE
  • Biopsi
Eksperimentel: MM2YA-EA01 Arm B (cytarabine, venetoclax)

Patients receive cytarabine IV and venetoclax PO on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.
Medicin: Cytarabine

Given IV

Andre navne:
  • Β-Cytosin arabinosid
  • 1-β-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-β-D-Arabinofuranosylcytosin
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosin
  • 1β-D-Arabinofuranosylcytosin
  • 2(1H)-pyrimidinon, 4-amino-1-beta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1P-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-celle
  • Arabine
  • Arabinofuranosylcytosin
  • Arabinosylcytosin
  • Aracytidin
  • Aracytin
  • Beta-Cytosin Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosin Arabinoside
  • Cytosin-β-arabinosid
  • Cytosin-beta-arabinosid
  • Erpalfa
  • Starasid
  • Tarabin PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Biopsy Procedure

Undergo biopsy

Andre navne:
  • Bx
  • BIOPSY_TYPE
  • Biopsi
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Eksperimentel: MM2YA-EA01 Arm C (Vyxeos, venetoclax)

Patients receive Vyxeos IV and venetoclax PO on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Biopsy Procedure

Undergo biopsy

Andre navne:
  • Bx
  • BIOPSY_TYPE
  • Biopsi
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Liposome-encapsulated Daunorubicin-Cytarabine

Given IV

Andre navne:
  • CPX-351
  • Cytarabin-Daunorubicin liposom til injektion
  • Daunorubicin og Cytarabin (liposomal)
  • Liposomal AraC-Daunorubicin CPX-351
  • Liposomal Cytarabin-Daunorubicin
  • Liposom-indkapslet kombination af Daunorubicin og Cytarabin
  • Vyxeos
  • Cytarabin og Daunorubicin Liposomal
  • CPX 351
  • CPX351
Eksperimentel: MM2YA-EA01 Arm D (azacitidine, venetoclax)

Patients receive azacitidine IV or SC and venetoclax PO on study. Patients undergo bone marrow aspiration and biopsy on study. Patients may also undergo ECHO and/or MUGA as clinically indicated.
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Biopsy Procedure

Undergo biopsy

Andre navne:
  • Bx
  • BIOPSY_TYPE
  • Biopsi
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Azacitidine

Given IV or SC

Andre navne:
  • 5 AZC
  • 5-AC
  • 5-Azacytidin
  • 5-AZC
  • Azacytidin
  • Azacytidin, 5-
  • Ladakamycin
  • Mylosar
  • U-18496
  • Vidaza
  • 5-azacitidin
Eksperimentel: MM3TCT-A03 Conditioning 1A (matched donors with venetoclax)

Patients receive venetoclax PO QD on days -10 to -2, fludarabine IV on days -6 or -5 to -2 and busulfan IV on days -3 to -2 or BID on days -5 to -2 or melphalan IV on day -2. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity. Patients undergo chest x-ray, echocardiography or MUGA during screening, and bone marrow biopsy and blood, urine and buccal swab collection throughout the study. Patients may also undergo PET scan and/or CT scan throughout the study.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Computed Tomography

Undergo CT

Andre navne:
  • CT
  • KAT
  • CAT-scanning
  • Beregnet aksial tomografi
  • Computerstyret aksial tomografi
  • Computerstyret tomografi
  • CT-scanning
  • tomografi
  • Computerstyret aksial tomografi (procedure)
  • Computerstyret tomografi (CT) scanning
  • Diagnostisk CAT -scanning
  • Diagnostic CAT Scan Service Type
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Positron Emission Tomography

Undergo PET

Andre navne:
  • Medicinsk billeddannelse, Positron Emission Tomografi
  • KÆLEDYR
  • PET-scanning
  • Positron Emission Tomografi Scan
  • Positron-emissionstomografi
  • PT
  • Positron emissionstomografi (procedure)
Medicin: Busulfan

Given IV

Andre navne:
  • Busulfex
  • Misulfan
  • Mitosan
  • Myeloleukon
  • Myelosan
  • 1,4-bis[methansulfonoxy]butan
  • BUS
  • Bussulfam
  • Busulfanum
  • Busulfan
  • CB 2041
  • CB-2041
  • Glyzophrol
  • GT 41
  • GT-41
  • Joacamine
  • Methansulfonsyre-tetramethylenester
  • Methansulfonsyre, tetramethylenester
  • Mielucin
  • Misulban
  • Myeleukon
  • Mylecytan
  • Myleran
  • Sulfabutin
  • Tetramethylen Bis(methansulfonat)
  • Tetramethylen bis[methansulfonat]
  • WR-19508
  • Busilvex
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Fludarabine

Given IV

Andre navne:
  • Fluradosa
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Procedure: Allogeneic Hematopoietic Stem Cell Transplantation

Given IV

Andre navne:
  • Allogen
  • Allogen hæmatopoietisk celletransplantation
  • Allogen stamcelletransplantation
  • HSC
  • HSCT
  • Stamcelletransplantation, Allogen
Procedure: Chest Radiography

Undergo chest x-ray

Andre navne:
  • Røntgen af ​​thorax
Medicin: Melphalan

Given IV

Andre navne:
  • CB-3025
  • L-PAM
  • L-Sarcolysin
  • Alanin nitrogen sennep
  • L-phenylalanin sennep
  • L-Sarcolysin Phenylalanin sennep
  • L-sarcolysin
  • Melphalanum
  • Phenylalanin sennep
  • Phenylalanin nitrogen sennep
  • Sarcoclorin
  • Sarkolysin
  • WR-19813
  • Melphalan til injektion-hepatisk leveringssystem
Placebo komparator: MM3TCT-A03 Conditioning 1B (matched donors with placebo)

Patients receive placebo PO QD on days -10 to -2, fludarabine IV on days -6 or -5 to -2 and busulfan IV on days -3 to -2 or BID on days -5 to -2 or melphalan IV on day -2. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity. Patients undergo chest x-ray, echocardiography or MUGA during screening, and bone marrow biopsy and blood, urine and buccal swab collection throughout the study. Patients may also undergo PET scan and/or CT scan throughout the study.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Computed Tomography

Undergo CT

Andre navne:
  • CT
  • KAT
  • CAT-scanning
  • Beregnet aksial tomografi
  • Computerstyret aksial tomografi
  • Computerstyret tomografi
  • CT-scanning
  • tomografi
  • Computerstyret aksial tomografi (procedure)
  • Computerstyret tomografi (CT) scanning
  • Diagnostisk CAT -scanning
  • Diagnostic CAT Scan Service Type
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Positron Emission Tomography

Undergo PET

Andre navne:
  • Medicinsk billeddannelse, Positron Emission Tomografi
  • KÆLEDYR
  • PET-scanning
  • Positron Emission Tomografi Scan
  • Positron-emissionstomografi
  • PT
  • Positron emissionstomografi (procedure)
Medicin: Busulfan

Given IV

Andre navne:
  • Busulfex
  • Misulfan
  • Mitosan
  • Myeloleukon
  • Myelosan
  • 1,4-bis[methansulfonoxy]butan
  • BUS
  • Bussulfam
  • Busulfanum
  • Busulfan
  • CB 2041
  • CB-2041
  • Glyzophrol
  • GT 41
  • GT-41
  • Joacamine
  • Methansulfonsyre-tetramethylenester
  • Methansulfonsyre, tetramethylenester
  • Mielucin
  • Misulban
  • Myeleukon
  • Mylecytan
  • Myleran
  • Sulfabutin
  • Tetramethylen Bis(methansulfonat)
  • Tetramethylen bis[methansulfonat]
  • WR-19508
  • Busilvex
Medicin: Fludarabine

Given IV

Andre navne:
  • Fluradosa
Medicin: Placebo Administration

Given PO

Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Procedure: Allogeneic Hematopoietic Stem Cell Transplantation

Given IV

Andre navne:
  • Allogen
  • Allogen hæmatopoietisk celletransplantation
  • Allogen stamcelletransplantation
  • HSC
  • HSCT
  • Stamcelletransplantation, Allogen
Procedure: Chest Radiography

Undergo chest x-ray

Andre navne:
  • Røntgen af ​​thorax
Medicin: Melphalan

Given IV

Andre navne:
  • CB-3025
  • L-PAM
  • L-Sarcolysin
  • Alanin nitrogen sennep
  • L-phenylalanin sennep
  • L-Sarcolysin Phenylalanin sennep
  • L-sarcolysin
  • Melphalanum
  • Phenylalanin sennep
  • Phenylalanin nitrogen sennep
  • Sarcoclorin
  • Sarkolysin
  • WR-19813
  • Melphalan til injektion-hepatisk leveringssystem
Eksperimentel: MM3TCT-A03 Conditioning 2A (haplo/mismatch with venetoclax)

Patients receive venetoclax PO QD on days -10 to -2, melphalan IV on day -6, fludarabine IV on days -5 to -2 and undergo total body irradiation once on day -1. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity. Patients undergo chest x-ray, echocardiography or MUGA during screening, and bone marrow biopsy and blood, urine and buccal swab collection throughout the study. Patients may also undergo PET scan and/or CT scan throughout the study.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Computed Tomography

Undergo CT

Andre navne:
  • CT
  • KAT
  • CAT-scanning
  • Beregnet aksial tomografi
  • Computerstyret aksial tomografi
  • Computerstyret tomografi
  • CT-scanning
  • tomografi
  • Computerstyret aksial tomografi (procedure)
  • Computerstyret tomografi (CT) scanning
  • Diagnostisk CAT -scanning
  • Diagnostic CAT Scan Service Type
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Positron Emission Tomography

Undergo PET

Andre navne:
  • Medicinsk billeddannelse, Positron Emission Tomografi
  • KÆLEDYR
  • PET-scanning
  • Positron Emission Tomografi Scan
  • Positron-emissionstomografi
  • PT
  • Positron emissionstomografi (procedure)
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Medicin: Fludarabine

Given IV

Andre navne:
  • Fluradosa
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Procedure: Allogeneic Hematopoietic Stem Cell Transplantation

Given IV

Andre navne:
  • Allogen
  • Allogen hæmatopoietisk celletransplantation
  • Allogen stamcelletransplantation
  • HSC
  • HSCT
  • Stamcelletransplantation, Allogen
Procedure: Chest Radiography

Undergo chest x-ray

Andre navne:
  • Røntgen af ​​thorax
Medicin: Melphalan

Given IV

Andre navne:
  • CB-3025
  • L-PAM
  • L-Sarcolysin
  • Alanin nitrogen sennep
  • L-phenylalanin sennep
  • L-Sarcolysin Phenylalanin sennep
  • L-sarcolysin
  • Melphalanum
  • Phenylalanin sennep
  • Phenylalanin nitrogen sennep
  • Sarcoclorin
  • Sarkolysin
  • WR-19813
  • Melphalan til injektion-hepatisk leveringssystem
Stråling: Total-Body Irradiation

Undergo total body irradiation

Andre navne:
  • Total kropsbestråling
  • TBI
  • SCT_TBI
  • Helkropsbestråling
  • Hele kroppen
Placebo komparator: MM3TCT-A03 Conditioning 2B (haplo/mismatch with placebo)

Patients receive placebo PO QD on days -10 to -2, melphalan IV on day -6, fludarabine IV on days -5 to -2 and undergo total body irradiation once on day -1. Patients then receive hematopoietic cell transplant IV on day 0. Treatment is given in the absence of disease progression or unacceptable toxicity. Patients undergo chest x-ray, echocardiography or MUGA during screening, and bone marrow biopsy and blood, urine and buccal swab collection throughout the study. Patients may also undergo PET scan and/or CT scan throughout the study.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Computed Tomography

Undergo CT

Andre navne:
  • CT
  • KAT
  • CAT-scanning
  • Beregnet aksial tomografi
  • Computerstyret aksial tomografi
  • Computerstyret tomografi
  • CT-scanning
  • tomografi
  • Computerstyret aksial tomografi (procedure)
  • Computerstyret tomografi (CT) scanning
  • Diagnostisk CAT -scanning
  • Diagnostic CAT Scan Service Type
Procedure: Echocardiography Test

Undergo ECHO

Andre navne:
  • Ekkokardiografi
  • EC
Procedure: Positron Emission Tomography

Undergo PET

Andre navne:
  • Medicinsk billeddannelse, Positron Emission Tomografi
  • KÆLEDYR
  • PET-scanning
  • Positron Emission Tomografi Scan
  • Positron-emissionstomografi
  • PT
  • Positron emissionstomografi (procedure)
Medicin: Fludarabine

Given IV

Andre navne:
  • Fluradosa
Medicin: Placebo Administration

Given PO

Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Procedure: Allogeneic Hematopoietic Stem Cell Transplantation

Given IV

Andre navne:
  • Allogen
  • Allogen hæmatopoietisk celletransplantation
  • Allogen stamcelletransplantation
  • HSC
  • HSCT
  • Stamcelletransplantation, Allogen
Procedure: Chest Radiography

Undergo chest x-ray

Andre navne:
  • Røntgen af ​​thorax
Medicin: Melphalan

Given IV

Andre navne:
  • CB-3025
  • L-PAM
  • L-Sarcolysin
  • Alanin nitrogen sennep
  • L-phenylalanin sennep
  • L-Sarcolysin Phenylalanin sennep
  • L-sarcolysin
  • Melphalanum
  • Phenylalanin sennep
  • Phenylalanin nitrogen sennep
  • Sarcoclorin
  • Sarkolysin
  • WR-19813
  • Melphalan til injektion-hepatisk leveringssystem
Stråling: Total-Body Irradiation

Undergo total body irradiation

Andre navne:
  • Total kropsbestråling
  • TBI
  • SCT_TBI
  • Helkropsbestråling
  • Hele kroppen
Eksperimentel: MM3TCT-A03 Maintenance I (venetoclax)

Patients receive venetoclax PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for up to 1 year post transplant (9 cycles) in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow biopsy and blood, urine and buccal swab collection throughout the study. Patients may also undergo PET scan and/or CT scan throughout the study.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Computed Tomography

Undergo CT

Andre navne:
  • CT
  • KAT
  • CAT-scanning
  • Beregnet aksial tomografi
  • Computerstyret aksial tomografi
  • Computerstyret tomografi
  • CT-scanning
  • tomografi
  • Computerstyret aksial tomografi (procedure)
  • Computerstyret tomografi (CT) scanning
  • Diagnostisk CAT -scanning
  • Diagnostic CAT Scan Service Type
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andre navne:
  • Blood Pool Scan
  • Ligevægtsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-scanning
  • Synkroniseret Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid Ventrikulogram Scan
  • Gated Heart Pool Scan
  • RNV Scan
Procedure: Positron Emission Tomography

Undergo PET

Andre navne:
  • Medicinsk billeddannelse, Positron Emission Tomografi
  • KÆLEDYR
  • PET-scanning
  • Positron Emission Tomografi Scan
  • Positron-emissionstomografi
  • PT
  • Positron emissionstomografi (procedure)
Medicin: Venetoclax

Given PO

Andre navne:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • ABT 199
  • GDC 0199
  • GDC0199
Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Placebo komparator: MM3TCT-A03 Maintenance II (placebo)

Patients receive placebo PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for up to 1 year post transplant (9 cycles) in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow biopsy and blood, urine and buccal swab collection throughout the study. Patients may also undergo PET scan and/or CT scan throughout the study.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navne:
  • Biopsi af knoglemarv
  • Biopsi, knoglemarv
Procedure: Computed Tomography

Undergo CT

Andre navne:
  • CT
  • KAT
  • CAT-scanning
  • Beregnet aksial tomografi
  • Computerstyret aksial tomografi
  • Computerstyret tomografi
  • CT-scanning
  • tomografi
  • Computerstyret aksial tomografi (procedure)
  • Computerstyret tomografi (CT) scanning
  • Diagnostisk CAT -scanning
  • Diagnostic CAT Scan Service Type
Procedure: Positron Emission Tomography

Undergo PET

Andre navne:
  • Medicinsk billeddannelse, Positron Emission Tomografi
  • KÆLEDYR
  • PET-scanning
  • Positron Emission Tomografi Scan
  • Positron-emissionstomografi
  • PT
  • Positron emissionstomografi (procedure)
Medicin: Placebo Administration

Given PO

Procedure: Biospecimen Collection

Undergo collection of blood, urine, and/or buccal swab samples

Andre navne:
  • Biologisk prøvesamling
  • Bioprøve indsamlet
  • Prøvesamling
  • Prøvekollektion
Eksperimentel: Screening (mutation carrier screening)

Patients undergo bone marrow aspiration and collection of blood on study. Patients' bone marrow and blood specimens undergo rapid genetic testing. Patients are then assigned to a specific substudy containing a therapy targeted to the patient's mutational profile. If there is no targetable mutation, the patient is placed on a substudy testing novel combinations that do not contain a target-specific drug. Patients who are not eligible for any MYELOMATCH substudy are assigned to TAP.
Procedure: Mutation Carrier Screening

Undergo rapid genetic testing
Eksperimentel: TAP (SOC treatment, mutation carrier screening)

Patients continue SOC treatment and undergo continued bone marrow aspiration and blood collection for possible future substudy assignment.
Andet: Best Practice

Receive SOC treatment

Andre navne:
  • plejestandard
  • standard terapi
Procedure: Mutation Carrier Screening

Undergo rapid genetic testing

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Timing of treatment Substudy or Tier Advancement Pathway (TAP) assignment
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will evaluate the feasibility of MATCHBox generating all data needed for assignment to a myeloMATCH clinical trial or determination that no assignment is available, within 72 hours of MDNet receipt of specimens for initial therapy and within 10 days for subsequent therapy. For first treatment assignment and separately for each subsequent treatment assignments: every 50 participants for the first 250 participants and then every 100 participants thereafter, the proportion of participants (cumulative and new participants since prior analysis) with all MDNet data needed to determine a treatment assignment within 72 hours for first assignment and 10 days for subsequent assignments after the MDNet receives specimens will be tallied.
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Time to MDNet generating all data required for treatment substudy or TAP assignment
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will be assessed within each tier of clinical trials, within each clinical basket of clinical trials, and over time (since last report and in 6 month intervals from study opening).
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Time to treatment substudy or TAP assignment
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will be assessed within each tier of clinical trials, within each clinical basket of clinical trials, and over time (since last report and in 6 month intervals from study opening).
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Percent assigned to a myeloMATCH clinical trial
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will be assessed within each tier of clinical trials, within each clinical basket of clinical trials, and over time (since last report and in 6 month intervals from study opening).
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Percent of screened participants who register to a treatment substudy
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will be assessed within each tier of clinical trials, within each clinical basket of clinical trials, and over time (since last report and in 6 month intervals from study opening).
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Assignment to higher tier treatment substudies within myeloMATCH
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will be assessed within each tier of clinical trials, within each clinical basket of clinical trials, and over time (since last report and in 6 month intervals from study opening).
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Adverse events
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will be assessed within each tier of clinical trials, within each clinical basket of clinical trials, and over time (since last report and in 6 month intervals from study opening).
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Minimal residual disease (MRD) response
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

MRD response is based on flow cytometry studies performed by the MDnet.
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Time-to-event outcomes for exploratory analysis
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Will be assessed within each tier of clinical trials, within each clinical basket of clinical trials, and over time (since last report and in 6 month intervals from study opening).
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy
Performance status
Tidsramme: Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Participants will be graded according to the Zubrod performance status scale.
Within 72 hours of MDNet receipt of specimens for initial therapy or within 10 days for subsequent therapy

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

National Cancer Institute (NCI)

Efterforskere

  • Ledende efterforsker: Jerald P Radich, SWOG Cancer Research Network

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

18. juni 2024

Primær færdiggørelse (Anslået)

15. maj 2029

Studieafslutning (Anslået)

15. maj 2029

Datoer for studieregistrering

Først indsendt

27. september 2022

Først indsendt, der opfyldte QC-kriterier

29. september 2022

Først opslået (Faktiske)

3. oktober 2022

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

2. november 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

30. oktober 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • NCI-2022-07006
  • U10CA180888 (U.S. NIH-bevilling/kontrakt)
  • NCI-2022-07006 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
  • MYELOMATCH (Anden identifikator: CTEP)
  • MYELOMATCH (Anden identifikator: SWOG)

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ja

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

produkt fremstillet i og eksporteret fra U.S.A.

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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