Condition: Acute Myeloid Leukemia · Myelodysplastic Syndrome · Sponsor: Bristol-Myers Squibb
The purpose of this study is to assess the safety, tolerability, drug levels, drug efficacy and determine the recommended dose of BMS-986497 as a monotherapy, in double combination with Azacitidine and in triple combination with Azacitidine and Venetoclax in participants with relapsed or refractory acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS).
This description comes directly from the study's public registry record.
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com · 855-907-3286 · Clinical.Trials@bms.com
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| Yale-New Haven Hospital | New Haven, Connecticut, United States | Recruiting |
| Northwestern Memorial Hospital | Chicago, Illinois, United States | Recruiting |
| Local Institution - 0007 | Boston, Massachusetts, United States | Withdrawn |
| Massachusetts General Hospital | Boston, Massachusetts, United States | Recruiting |
| Washington University School of Medicine, Siteman Cancer Center | St Louis, Missouri, United States | Recruiting |
| John Theurer Cancer Center at Hackensack University Medical Center | Hackensack, New Jersey, United States | Recruiting |
| Columbia University Irving Medical Center | New York, New York, United States | Withdrawn |
| University of Texas MD Anderson Cancer Center | Houston, Texas, United States | Recruiting |
| Local Institution - 0009 | Fairfax, Virginia, United States | Withdrawn |
| Princess Margaret Cancer Centre | Toronto, Ontario, Canada | Recruiting |
| Jewish General Hospital | Montreal, Quebec, Canada | Recruiting |
| Local Institution - 0017 | Marseille, Bouches-du-Rhône, France | Not Yet Recruiting |
+ 4 more locations — full list on the registry record.
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