- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT07563010
Menin-Inhibitor Targeted Maintenance in AML
Phase 2 Randomized Controlled Study of Revumenib as Maintenance Therapy After Allogeneic Hematopoietic Stem Cell Transplantation in Patients With KMT2Ar, NPM1m, or NUP98r Acute Myeloid Leukemia (AML)
Tutkimuksen yleiskatsaus
Tila
Ehdot
Interventio / Hoito
Yksityiskohtainen kuvaus
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Vaihe
- Vaihe 2
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Paul Guo
- Puhelinnumero: 4583 7634064583
- Sähköposti: pguo@nmdp.org
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Kuvaus
Inclusion Criteria:
Inclusion Criteria:
- Aged ≥18 years at the time of signing informed consent
- Able to provide written informed consent personally or via a legally authorized representative in accordance with applicable regulatory and institutional requirements
- Willing and able to comply with all study procedures and available for the duration of the study
- Diagnosis of acute myeloid leukemia (AML) in complete morphologic remission with one of the following molecular abnormalities:
1. KMT2A-rearranged (KMT2Ar) AML (Excluding KMT2A partial tandem duplication (KMT2A-PTD) 2. NPM1-mutated (NPM1m) AML (Including FLT3-ITD or TKD co-mutation) 3. NUP98-rearranged (NUP98r) AML 5. Planned first allogeneic hematopoietic cell transplantation (allo-HCT) for AML.
6. Transplant Characteristics
- Planned allo-HCT using bone marrow or peripheral blood stem cell graft source.
- Planned reduced-intensity/non-myeloablative conditioning (RIC/NMA) or myeloablative conditioning (MAC), using a conditioning regimen permitted- by the protocol and consistent with standard clinical practice, meeting CIBMTR criteria for conditioning intensity
7. Planned donor:
- HLA-matched related donor (5/6 or 6/6)
- Matched unrelated donor (8/8)
- Mismatched unrelated donor (7/8)
- Haploidentical donor meeting institutional requirements
8. Performance Status:
1. Karnofsky Performance Status ≥70%. 9. Cardiac Function: left ventricular ejection fraction (LVEF) by transthoracic echocardiogram (TTE) or multigated acquisition (MUGA) with no clinical evidence of heart failure: RIC/NMA: ≥50% MAC: ≥5 10. Pulmonary function meeting the following criteria, without supplemental oxygen other than CPAP:
- RIC/NMA: DLCO (corrected for hemoglobin) and FEV1 ≥40% predicted
- MAC: DLCO and FEV1 ≥50% predicted
11. Renal Function: estimated creatinine clearance (CrCl) ≥45mL/min calculated using the Cockcroft-Gault formula or 24-hour urine collection, consistent with standard eligibility criteria for allogeneic HCT recipients.
12. Liver function acceptable per local institutional guidelines for allo-HCT eligibility.
13. Reproductive Status: Willingness to use contraception in accordance with local regulations from first study intervention through the required contraceptive period Willingness to use contraception in accordance with local regulations from first study intervention through the required contraceptive period
Exclusion Criteria:
Disease Status:
a. Evidence of active AML prior to HCT, assessed within 42 days before transplant, defined as any of the following:
- ≥5% bone marrow blasts
- Circulating blasts within 14 days before conditioning
- CNS or other extramedullary disease
- Other active malignancy that, in the investigator's judgment, could interfere with safety or efficacy assessment
- Treatment with non-protocol antileukemic therapy (donor lymphocyte infusion for relapse prophylaxis or treatment will be considered an EFS event)
Cardiac / QT Risk
- Requirement for concomitant medications known to prolong QT/QTc interval, except low-risk agents used as standard supportive care
- Diagnosis or suspicion of Long QT syndrome, or a family history of Long QT syndrome
- Fridericia's corrected QT interval (QTcF) >450 msec.
- History within 6 months of study entry of:
i. Myocardial infarction ii. Unstable angina iii. Congestive heart failure (NYHA Class ≥ II) iv. Life-threatening or uncontrolled arrhythmia v. Cerebrovascular accident or transient ischemic attack
- Chronic respiratory disease requiring continuous supplemental oxygen, or other significant organ dysfunction that would adversely affect study participation.
Active, uncontrolled infection, including any of the following:
- Active, uncontrolled systemic fungal, bacterial, or viral infection within 14 days prior to the start of conditioning
- Any other documented active, uncontrolled infection at the start of conditioning
Chronic viral infections with evidence of active disease, including:
HIV: detectable viral load within 6 months prior to screening
Hepatitis B:
- HBsAg-positive and/or anti-HBc-positive with detectable HBV DNA
- Anti-HBc-positive alone Hepatitis C: positive HCV antibody with detectable HCV RNA
- Planned HCT using cord blood, ex vivo T cell depletion, engineered grafts, or experimental graft sources
Malabsorption syndrome or GI condition that precludes oral administration, including:
- Inability to swallow oral medications
- Prior gastric bypass or severe gastroparesis
- Cirrhosis with Child-Pugh Class B or C
- Pregnant or breastfeeding
- Prior intolerance to menin inhibitor therapy resulting in ≥ Grade 3 treatment-related adverse events
- Any condition, therapy, laboratory abnormality, or allergy to excipients that, in the investigator's judgment, could confound study results, interfere with the participant's ability to comply with study procedures or complete the study, or make participation not in the participant's best interest.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Tukevaa hoitoa
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Kolminkertaistaa
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: Revumenib BID
For patients not taking strong CYP3A4 inhibitor and patients taking strong CYP3A4 inhibitor
|
oral tablets
Muut nimet:
|
|
Placebo Comparator: Placebo BID
For patients not taking strong CYP3A4 inhibitor and patients taking strong CYP3A4 inhibitor
|
suun kautta otettavat tabletit
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Relapse free survival (RFS) in KMT2Ar, NPM1m, and NUP98r AML in the Intent-to-Treat (ITT) population with a minimum of 1 year of follow-up post-randomization.
Aikaikkuna: From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
RFS is defined as the time from randomization to the date of relapse or the date of death from any cause, whichever comes first.
|
From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
RFS in the modified ITT (mITT) population
Aikaikkuna: From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization
|
Relapse free survival rate in modified intent to treat population
|
From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization
|
|
Rate of overall survival (OS) in the ITT population
Aikaikkuna: From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
Overall survival rate in the intent-to-treat population
|
From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
|
Incidence of relapse in the ITT population
Aikaikkuna: From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
Incidence of relapses in intent-to-treat participant population
|
From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
|
Rate of event-free survival (EFS) in the ITT population
Aikaikkuna: From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization
|
Events such as relapse/progression, death from any cause, graft failure, use of donor lymphocyte infusion which have occurred from time from the date of randomization to the date of event occurrence.
|
From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization
|
|
Rate of non-relapse mortality (NRM) in the ITT population
Aikaikkuna: From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
Death in participants in the absence of disease progression or relapse
|
From randomization to the date of event occurrence, assessed for a minimum of 1 year post-randomization.
|
|
Frequency, duration, and severity of Treatment-Emergent Adverse Events (TEAEs), Treatment-Related Adverse Events (TRAEs), Adverse Events of Special Interest (AESIs), and Serious Adverse Events (SAEs) in the Safety Analysis population
Aikaikkuna: From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization
|
Documentation of number of treatment related of adverse events; their frequencies, duration, and severity
|
From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization
|
|
Change from baseline in other observations related to safety for electrocardiograms (ECGs) measuring QT intervals.
Aikaikkuna: From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization.
|
Documentation and comparison of abnormal ECGs from baseline measurements in relationship to safety
|
From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization.
|
|
Change from baseline in other observations related to safety for vital signs.
Aikaikkuna: From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization.
|
Documentation and comparison of abnormal vital signs from baseline measurements in relationship to safety
|
From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization.
|
|
Change from baseline in other observations related to safety for performance status in the Safety Analysis population
Aikaikkuna: From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization.
|
Documentation and comparison of abnormal performance from baseline measurements in relationship to safety
|
From date of randomization to end of treatment, assessed for a minimum of 1 year post-randomization.
|
Yhteistyökumppanit ja tutkijat
Tutkijat
- Opintojen puheenjohtaja: Steven Devine, M.D, NMDP
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Ensisijainen valmistuminen (Arvioitu)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
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