This study is in progress, not accepting new patients

TL-895 and KRT-232 Study in Acute Myeloid Leukemia

a study on Acute Myeloid Leukemia Leukemia

Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Orange, California and other locations
Dates
study started
estimated completion

Description

Summary

This study evaluates TL-895, a potent, orally available and highly selective irreversible tyrosine kinase inhibitor combined with navtemadlin (KRT-232), a novel oral small molecule inhibitor of MDM2 for the treatment of adults with FLT3 mutated Acute Myeloid Leukemia. Participants must be relapsed/refractory (e.g., having failed prior therapy) to be eligible for this study.

Official Title

An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of TL-895 Combined With KRT-232 in Patients With Relapsed/Refractory (R/R) FLT3+ Acute Myeloid Leukemia (AML)

Keywords

Acute Myeloid Leukemia, AML, TP53, FLT3+, Navtemadlin, Leukemia, Myeloid Leukemia, Leukemia, Myeloid, Acute, KRT-232

Eligibility

You can join if…

Open to people ages 18 years and up

  • TP53 wildtype AML
  • Relapsed/Refractory to at least one prior therapy, one of which must have included a FLT-3 inhibitor
  • FLT3 mutation (FLT3-TKD or FLT3-ITD)
  • ECOG 0-2
  • Adequate hematologic, hepatic, and renal functions

You CAN'T join if...

  • AML subtype 3
  • Prior treatment with MDM2 antagonist therapies
  • Eligible for HSCT

Locations

  • University of California, Irvine Medical Center
    Orange California 92868 United States
  • Keck School of Medicine
    Los Angeles California 90033 United States

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Telios Pharma, Inc.
ID
NCT04669067
Phase
Phase 1/2 research study
Study Type
Interventional
Participants
About 18 people participating
Last Updated