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Spots Global Cancer Trial Database for A Phase 1, Study of BMF-500 in Adults With Acute Leukemia

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Trial Identification

Brief Title: A Phase 1, Study of BMF-500 in Adults With Acute Leukemia

Official Title: A Phase 1, Open-label, Dose-escalation, and Dose-expansion Study of BMF-500, an Oral Covalent FLT3 Inhibitor, in Adults With Acute Leukemia

Study ID: NCT05918692

Interventions

BMF-500

Study Description

Brief Summary: A Phase 1 first-in-human dose-escalation and dose-expansion study of BMF-500, an oral FLT3 inhibitor, in adult patients with acute leukemia.

Detailed Description: A Phase 1 first-in-human dose-escalation and dose-expansion study of BMF-500, an oral covalent FLT3 inhibitor, in adult patients with acute myeloid leukemia (AML), acute lymphocytic leukemia (ALL) and Acute Mixed-Phenotype Leukemia (MPAL) who may or may not be on Antifungals.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic, Phoenix, Arizona, United States

City of Hope National Medical Center, Duarte, California, United States

UCLA Department of Medicine, Los Angeles, California, United States

University of California, Davis, Sacramento, California, United States

University of California, San Francisco, San Francisco, California, United States

Colorado Blood Cancer Institute, Denver, Colorado, United States

Mayo Clinic, Jacksonville, Florida, United States

Winship Cancer Institute, Emory University, Atlanta, Georgia, United States

Northwestern Memorial Hospital, Chicago, Illinois, United States

University of Chicago Duchossois Center for Advanced Medicine (DCAM), Chicago, Illinois, United States

University of Kentucky - Markey Cancer Center, Lexington, Kentucky, United States

Mayo Clinic, Rochester, Minnesota, United States

John Theurer Cancer Center, Hackensack, New Jersey, United States

Montefiore Hospital - Moses Campus - BRANY - PPDs, Bronx, New York, United States

Roswell Park Comprehensive Cancer Center, Buffalo, New York, United States

Northwell Health Cancer Institute, New Hyde Park, New York, United States

East Carolina University, Greenville, North Carolina, United States

Cleveland Clinic Hospital, Cleveland, Ohio, United States

University of Oklahoma - Stephenson Cancer Center, Oklahoma City, Oklahoma, United States

Texas Oncology-PA USOR, Dallas, Texas, United States

MD Anderson Cancer Center, Houston, Texas, United States

Virginia Cancer Specialists, Gainesville, Virginia, United States

Fred Hutchinson Cancer Center, Seattle, Washington, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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