BMF-500 is under clinical development by Biomea Fusion and currently in Phase I for Relapsed Acute Myeloid Leukemia. According to GlobalData, Phase I drugs for Relapsed Acute Myeloid Leukemia have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how BMF-500’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
BMF-500 overview
BMF-500 is under development for the treatment of relapsed and refractory acute myeloid leukemia (AML), acute mixed phenotype leukemia (MPAL) and acute lymphocytic leukemia (ALL). They are administered though oral route. The drug candidate acts by targeting third-generation Fms-like tyrosine kinase 3 (FLT3). The drug candidates are being developed based on Fusion System platform.
Biomea Fusion overview
Biomea Fusion is a precision oncology company dedicated to developing innovative medicines targeting genomically defined alterations in both hematologic and solid cancers. The company is headquartered in Palo Alto, California, the US.
For a complete picture of BMF-500’s drug-specific PTSR and LoA scores, buy the report here.
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