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Clinical Trials in the EU / 2024-519537-29-00
Authorised Phase I

A Phase I Study of BMS-986497 alone or in combination with Azacitidine (Aza) and Azacitidine plus Venetoclax (AZA+VEN) in relapsed or refractory (R/R) AML or MDS

2024-519537-29-00 · tracked via the Priya Life Science EU tracker
Sponsor
Bristol-Myers Squibb Services Unlimited Company
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
26/09/2025
Enrollment target
35
Sites
France, Spain

Condition studied

Acute Myeloid Leukemia and Myelodysplastic Syndrome

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2024-519537-29-00 on CTIS ↗ ← All trials in the EU