drugset / Trial / NCT06001788

Safety and Tolerability of Ziftomenib Combinations in Patients With Relapsed/Refractory Acute Myeloid Leukemia

NCT06001788

Phase 1 Recruiting 171 enrolled Kura Oncology, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The safety, tolerability, and antileukemic response of ziftomenib in combination with standard of care treatments for patients with relapsed/refractory acute myeloid leukemia will be examined with the following agents: FLAG-IDA, low-dose cytarabine, and gilteritinib.

Timeline

Start
2024-02-22
Primary completion
2026-08
Completion
2027-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Ziftomenib Small molecule Oral
Background Cytarabine Small molecule Intravenous
Background Fludarabine Small molecule Intravenous
Background Gilteritinib Small molecule Oral
Background Granulocyte colony-stimulating factor Protein / enzyme biologic Subcutaneous
Background Idarubicin Small molecule Intravenous