- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01323751
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma (ACY-1215)
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Phase 1(a & b): To evaluate the side effects and determine the best dose of oral ACY-1215 as monotherapy, and also in combination with bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma.
Phase 2a: To determine the objective response rate of oral ACY-1215 in combination with bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma.
Studieoversigt
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Studiesteder
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Georgia
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Atlanta, Georgia, Forenede Stater, 30322
- Winship Cancer Institute, Emory University
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Massachusetts
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Boston, Massachusetts, Forenede Stater, 02115
- Massachusetts General Hospital
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New York
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New York, New York, Forenede Stater, 10029
- Mt. Sinai Medical Center
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Pennsylvania
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Philadelphia, Pennsylvania, Forenede Stater, 19104
- University of Pennsylvania
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Texas
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Houston, Texas, Forenede Stater, 77030
- MD Anderson Cancer Center
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Wisconsin
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Milwaukee, Wisconsin, Forenede Stater, 53226
- Medical College of Wisconsin - Clinical Cancer Center
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-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
Patient has relapsed or relapsed/refractory MM with measurable disease parameters according to the International Myeloma Working Group (IMWG) Criteria
- Refractory is defined as experiencing less than minimal response (MR) to or progressive disease (PD) within 60 days after completion of the most recent anti-MM regimen
- Relapsed is defined as experiencing PD that requires therapy but which is not refractory following the achievement of stable disease (SD) or better to the most recent anti-MM regimen.
- Patient received at least 2 prior regimens for MM.
- Patient received prior treatment for MM with a proteasome inhibitor and an immunomodulatory drug, unless not a candidate for a proteasome inhibitor or an immunomodulatory drug.
- Patient either is not a candidate for autologous stem cell transplant (ASCT), has declined the option of ASCT, or has relapsed after prior ASCT.
- Patient is ≥18 years of age.
- Patient has a Karnofsky Performance Status score of ≥70
Patient has adequate bone marrow reserve, as evidenced by:
- Absolute neutrophil count (ANC) of ≥1.0x109/L.
- Platelet count of ≥ 75x109/L in patients in whom <50% of bone marrow nucleated cells are plasma cells and ≥50x109/L in patients in whom more than 50% of bone marrow nucleated cells are plasma cells.
- Patient has adequate renal function (calculated creatinine clearance of ≥30 mL/min according to the Cockroft-Gault)
- Patient has adequate hepatic function (serum bilirubin values <2.0 mg/dL and ALT and/or AST values <3 × the upper limit of normal ULN).
- Patient has a corrected serum calcium ≤ULN.
Exclusion Criteria
Patient has received any of the following therapies:
- Radiotherapy or systemic therapy within 2 weeks of baseline
- Prior peripheral autologous stem cell transplant within 12 wks of Baseline.
- Prior allogeneic stem cell transplant.
- Prior treatment with an HDAC inhibitor.
- Patient has an active systemic infection requiring treatment.
- Patient has a history of other malignancies unless has undergone definitive treatment more than 5 yrs prior to study and without evidence of recurrent malignant disease (excluding basal cell carcinoma of the skin; superficial carcinoma of the bladder; carcinoma of the prostate with a current prostate-specific antigen <0.1 ng/mL; or cervical intraepithelial neoplasia).
- Patient has known or suspected HIV, positive for hepatitis B or is known or suspected to have active hepatitis C infection.
- Patient has a history of significant cardiovascular, neurological, endocrine, gastrointestinal, respiratory, or inflammatory illness including recent myocardial infarction (within 6 months)or stroke; hypertension requiring >2 medications for adequate control; diabetes mellitus with >2 episodes of ketoacidosis in the preceding 12 months; or chronic obstructive pulmonary disease (COPD) requiring >2 hospitalizations in the preceding 12 months.
- Patient has a QTcF value of >480 msec; family or personal history of long QTc syndrome or ventricular arrhythmias including ventricular bigeminy; previous history of drug-induced QTc prolongation
- Patient has > Grade 2 painful neuropathy or peripheral neuropathy
- Patient has a history of allergic reaction attributable to bortezomib or other compounds containing boron or mannitol (Phase 1b and 2a only)
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Treat Regimen
ACY-1215 Bortezomib Dexamethasone
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Liquid oral dose on Days 1-5 and 8-12 of 21-day treatment cycle
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Phase 1 (a & b): To determine the maximum tolerated dose of ACY-1215 as monotherapy or in combination with bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma.
Tidsramme: Upon completion of 21-day treatment cycle
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Upon completion of 21-day treatment cycle
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Phase 2a: To determine the objective response rate to ACY-1215 in combination with bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma.
Tidsramme: Assessed every other treatment cycle (cycles 2, 4 and 6)
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Assessed every other treatment cycle (cycles 2, 4 and 6)
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Characterize the safety of ACY-1215 alone or in combination with bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma
Tidsramme: Up to 24 weeks
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Up to 24 weeks
|
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Determine the single- and multiple-dose PK of ACY-1215 alone and in combination with bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma
Tidsramme: Upon completion of 21 day treatment cycle
|
Upon completion of 21 day treatment cycle
|
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Evaluate the pharmacodynamics of ACY-1215 alone or in combination with bortezomib and dexamethasone in patients with relapsed or relapsed/refractory multiple myeloma.
Tidsramme: Up to 24 weeks.
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Up to 24 weeks.
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Sagar Lonial, MD, Winship Cancer Institute, Emory University
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Hjerte-kar-sygdomme
- Karsygdomme
- Sygdomme i immunsystemet
- Neoplasmer efter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Immunproliferative lidelser
- Hæmatologiske sygdomme
- Hæmoragiske lidelser
- Hæmostatiske lidelser
- Paraproteinæmier
- Blodproteinforstyrrelser
- Myelomatose
- Neoplasmer, Plasmacelle
- Molekylære mekanismer for farmakologisk virkning
- Enzymhæmmere
- Antineoplastiske midler
- Histon deacetylase hæmmere
- Ricolinostat
Andre undersøgelses-id-numre
- ACY-100
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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 .
Kliniske forsøg med Myelomatose
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Guangzhou Bio-gene Technology Co., LtdTrukket tilbageMultiple myeloma -ildfast
-
University Health Network, TorontoIkke rekrutterer endnuMyelom i tilbagefald | Multiple myeloma -ildfastCanada
-
Hebei Senlang Biotechnology Inc., Ltd.Peking University People's Hospital; Institute of Hematology & Blood Diseases...Ikke rekrutterer endnuMyelom i tilbagefald | Multiple myeloma -ildfast
-
Baskent UniversityIkke rekrutterer endnuMULTIPL SKLEROSETyrkiet (Türkiye)
-
Minsk Scientific-Practical Center for Surgery,...RekrutteringAnti-BCMA CAR-T-celleterapi for voksne med tilbagevendende eller refraktær myelomatose (MSTH-CAR001)Multiple myeloma -ildfastHviderusland
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HuniLife Biotechnology, Inc.Tilmelding efter invitationMultiple myeloma -ildfastTaiwan
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CHU de Quebec-Universite LavalRekrutteringRecidiverende myelomatose | Multiple myeloma -ildfastCanada
-
PETHEMA FoundationRekrutteringDe novo multiple myeloma | Anitocabtagene AutoleucelSpanien
-
CellCentric Ltd.RekrutteringMyelom i tilbagefald | Multiple myeloma -ildfastForenede Stater, Det Forenede Kongerige
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Asan Medical CenterAfsluttetAkut leukæmi, myelodysplastisk syndrom, myeloproliferative neoplasmer, lymfom, multiple myelomaSydkorea
Kliniske forsøg med ACY-1215
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-
Acetylon Pharmaceuticals IncorporatedAfsluttetSund og raskForenede Stater
-
Regenacy Pharmaceuticals LLCAfsluttetSmertefuld diabetisk perifer neuropatiForenede Stater
-
Columbia UniversityNational Cancer Institute (NCI); Acetylon Pharmaceuticals IncorporatedAfsluttetMetastatisk brystkræft | BrystkarcinomForenede Stater
-
CelgeneAfsluttet
-
Dana-Farber Cancer InstituteAcetylon Pharmaceuticals IncorporatedAktiv, ikke rekrutterendeTilbagevendende kronisk lymfoid leukæmiForenede Stater
-
National Institute of Allergy and Infectious Diseases...ModernaTX, Inc.Afsluttet
-
CelgeneAfsluttetAvancerede solide tumorerForenede Stater
-
Dana-Farber Cancer InstituteCelgene CorporationAfsluttetLivmoderhalskræft | Æggelederkræft | Primært peritonealt karcinomForenede Stater
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CelgeneAfsluttetMyelomatoseForenede Stater