CompletedPHASE1, PHASE2NCT03072043
Phase 1b/2 Safety and Efficacy of APR-246 w/Azacitidine for tx of TP53 Mutant Myeloid Neoplasms
Studying Acute myelomonocytic leukemia
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
- H. Lee Moffitt Cancer Center and Research Institute
- Principal Investigator
- David Sallman, M.D.H. Lee Moffitt Cancer Center and Research Institute
- Intervention
- APR-246(drug)
- Enrollment
- 55 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2017 – 2021
Study locations (6)
- H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, United States
- The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- Weill Medical College of Cornell University, New York, New York, United States
- Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, United States
- University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States
Collaborators
Aprea Therapeutics
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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