RecruitingPhase 1NCT06419634
Study of BMS-986497 (ORM-6151) as a Monotherapy, in Double and Triple Combination With Azacitidine and Venetoclax in Participants With Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Bristol-Myers Squibb
- Principal Investigator
- Bristol-Myers SquibbBristol-Myers Squibb
- Intervention
- BMS-986497(drug)
- Enrollment
- 105 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2030
Study locations (15)
- Yale-New Haven Hospital, New Haven, Connecticut, United States
- Northwestern Memorial Hospital, Chicago, Illinois, United States
- Local Institution - 0007, Boston, Massachusetts, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Washington University School of Medicine, Siteman Cancer Center, St Louis, Missouri, United States
- John Theurer Cancer Center at Hackensack University Medical Center, Hackensack, New Jersey, United States
- Columbia University Irving Medical Center, New York, New York, United States
- University of Texas MD Anderson Cancer Center, Houston, Texas, United States
- Local Institution - 0009, Fairfax, Virginia, United States
- Princess Margaret Cancer Centre, Toronto, Ontario, Canada
- Jewish General Hospital, Montreal, Quebec, Canada
- Local Institution - 0017, Marseille, Bouches-du-Rhône, France
- Local Institution - 0018, Paris, France
- Local Institution - 0022, Toulouse, France
- Local Institution - 0020, Barcelona, Catalunya [Cataluña], Spain
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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