drugset / Trial / NCT04477291

A Study of CG-806 in Patients With Relapsed or Refractory AML or Higher-Risk MDS

NCT04477291 ↗

Phase 1 Terminated 45 enrolled Aptose Biosciences Inc.
NaSequentialOpen-labelTreatment

Summary

This study is being done to evaluate the safety, tolerability and antitumor activity of oral CG-806 (luxeptinib) for the treatment of patients with Acute Myeloid Leukemia (except APML), secondary AML, therapy-related AML, or higher-risk MDS, whose disease has relapsed, is refractory or who are ineligible for or intolerant of intensive chemotherapy or transplantation.

Timeline

Start
2020-10-06
Primary completion
2024-04-15
Completion
2024-04-15

Outcome

Outcome not reported

Stopped (Business): “Change in corporate strategy”

Drugs

EvaluationDrugModalityDoseRoute
Subject luxeptinib Small molecule 450 mg Oral