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

Phase 1
Recruiting
Conditions
Acute Myeloid Leukemia
Interventions
Registration Number
NCT05918692
Lead Sponsor
Biomea Fusion Inc.
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), who may or may not be on Antifungals.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
84
Inclusion Criteria
  • Age ≥ 18 years.
  • Individuals with histologically or pathologically confirmed diagnosis of relapsed or refractory AML with documented FLT3 mutation, and/or Individuals with histologically or pathologically confirmed diagnosis of their malignancy with wild-type FLT3 (including those with MLL1-R and NPM1 mutations).
  • ECOG performance status of 0-2.
  • Adequate liver and renal function
  • Adhere to the CYP3A4 inhibitor concomitant therapy use requirements, as follows:
  • Arm A: Participants must not have received a moderate or strong CYP3A4 inhibitor for at least 7 days prior to enrollment and are not anticipated to require such agents in the near term (for at least 4 weeks).
  • Arm B: Participants must have received a necessary azole antifungal(s) that is a strong CYP3A4 inhibitor (excluding other strong CYP3A4 inhibitor[s]) for at least 7 days prior to enrollment and be able to continue such azole antifungal(s) while on BMF-500 treatment for at least 4 weeks.
  • Arm C: Participants must have received necessary azole antifungal(s) that are moderate CYP3A4 inhibitors (excluding other moderate CYP3A4 inhibitors) for at least 7 days prior to enrollment and be able to continue such azole antifungal(s) while on BMF-500 treatment for at least 4 weeks (Cycle 1).

Key

Exclusion Criteria
  • Significant cardiovascular disease including unstable angina pectoris, uncontrolled hypertension or arrhythmia, history of cerebrovascular accident including transient ischemic attack within 6 months prior to the first dose of the trial intervention.
  • WBC count >50,000/µL (uncontrollable with cytoreductive therapy).
  • Women who are pregnant or lactating or plan to become pregnant.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm A: Escalation PhaseBMF-500BMF-500 taken twice daily by participants who are not receiving drugs that inhibit CYP3A4 activity.
Arm B: Escalation PhaseBMF-500BMF-500 taken twice daily by participants who are receiving necessary azole antifungals that are Strong CYP3A4 inhibitors.
Arm C: Escalation PhaseBMF-500BMF-500 taken twice daily by participants who are receiving necessary azole antifungals that are moderate CYP3A4 inhibitors.
Primary Outcome Measures
NameTimeMethod
Evaluate the safety and tolerability of BMF-500 by incidence of Serious Adverse Events (SAEs).At the end of each 28 Day cycle for a maximum of 32 cycles

Assessed by the NCI CTCAE version 5.0.

Determine the recommended Phase 2 Dose (RP2D) of BMF-500.At the end of 28 day Dose-Limiting Toxicities (DLT) observation Period

Pharmacovigilance (PK) at each dose level as determined by area under the curve plasma concentration from time 0 to last quantifiable concentration (AUClast).

Evaluate the safety and tolerability of BMF-500 by incidence of Treatment Emergent Adverse Events (TEAEs).At the end of each 28 Day cycle for a maximum of 32 cycles

Assessed by the NCI CTCAE version 5.0.

Secondary Outcome Measures
NameTimeMethod
Determine the pharmacokinetics of BMF-500.At the end of Cycle 1 and 2 (each cycle is 28 days in duration)

Area under the curve plasma concentration from time 0 to last quantifiable concentration (AUClast).

Evaluate the efficacy of BMF-500At the end of each cycle (each cycle is 28 days in duration) for a maximum of 32 cycles

Overall Reasons Rate (ORR).

Assess additional evidence of antitumor activity per investigator assessment as per corresponding response criteria.At the end of each cycle (each cycle is 28 days in duration) for a maximum of 32 cycles

Overall Survival (OS).

Trial Locations

Locations (21)

Mayo Clinic

🇺🇸

Rochester, Minnesota, 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

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

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Mayo Clinic
🇺🇸Rochester, Minnesota, United States

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