A Safety and Efficacy Study of CC-90009 Combinations in Subjects With Acute Myeloid Leukemia
NCT04336982 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 22
Last updated 2024-05-31
Summary
CC-90009-AML-002 is an exploratory Phase 1b, open-label, multi-arm trial to evaluate the safety and efficacy of CC-90009 in combination with anti-leukemia agents in participants with acute myeloid leukemia (AML).
Conditions
- Leukemia, Myeloid, Acute
Interventions
- DRUG
-
CC-90009
Injection
- DRUG
-
Tablet
- DRUG
-
Injection
- DRUG
-
Gilteritinib
Tablet
Sponsors & Collaborators
- collaborator INDUSTRY
-
Celgene
lead INDUSTRY
Principal Investigators
-
Bristol-Myers Squibb · Bristol-Myers Squibb
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-08-05
- Primary Completion
- 2023-10-25
- Completion
- 2024-04-05
- FDA Drug
- Yes
Countries
- United States
- Belgium
- Canada
- France
- United Kingdom
Study Locations
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