Overview

Study of FF-10101-01 in Patients With Relapsed or Refractory Acute Myeloid Leukemia

Status:
Active, not recruiting
Trial end date:
2023-01-01
Target enrollment:
Participant gender:
Summary
A Phase 1/2a dose escalation and dose ranging study of FF-10101-01 in subjects with relapsed or refractory acute myeloid leukemia to determine the safety, tolerability, PK and preliminary efficacy. A total of 9 cohorts will be enrolled in Phase 1 to establish the Maximum Tolerated Dose (MTD). Phase 2a will consist of up to 3 dose levels (high, medium, and low) of which subjects with FLT3 mutations will randomly be assigned.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Fujifilm Pharmaceuticals U.S.A., Inc.
Treatments:
FF-10101