drugset / Trial / NCT04687761

Clinical Trial to Assess the Safety and Tolerability of the Combination of Low-dose Cytarabine or Azacitidine Plus Venetoclax and Quizartinib in Newly Diagnosed AML Patients Aged Equal or More Than 60 Years Old

NCT04687761

Phase 1/2 Completed 113 enrolled PETHEMA Foundation
RandomizedParallel-groupOpen-labelTreatment

Summary

A phase I-II trial based on the combination of three drugs regimen LDAC or Azacitidine + Venetoclax + Quizartinib that in this population could be well tolerated by a sequential type administration. The first objective is to achieve rapid control of the disease, using two different schemes, one based in Azacitidine and the other in LDAC, by dose escalation in phase I of the trial. The second goal is to prevent relapse through a maintenance schedule. Phase II will study the efficacy and safety of the recommended dose for Phase II

Timeline

Start
2020-11-04
Primary completion
2024-11-30
Completion
2025-05-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified 75 mg/m2 Subcutaneous
Subject Cytarabine Small molecule 20 mg/m2 Subcutaneous
Subject Quizartinib Small molecule 30 mg Oral
Subject Quizartinib Small molecule 40 mg Oral
Subject Quizartinib Small molecule 60 mg Oral
Subject Venetoclax Small molecule 400 mg Oral
Subject Venetoclax Small molecule 600 mg Oral