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Active Not RecruitingNCT05918692

A Phase 1 Study of BMF-500 in Adults With Acute Leukemia

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

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Biomea Fusion Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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), who may or may not be on Antifungals.

Conditions

Interventions

TypeNameDescription
DRUGBMF-500Investigational Product

Timeline

Start date
2023-07-26
Primary completion
2026-04-01
Completion
2026-04-01
First posted
2023-06-26
Last updated
2026-02-23

Locations

14 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05918692. Inclusion in this directory is not an endorsement.