drugset / Trial / NCT05662956

A Clinical Study of VA-CAG as Induction Therapy in Newly Diagnosed AML Patients

NCT05662956

Phase 2 Completed 114 enrolled Hematology department of the 920th hospital
NaSingle-groupOpen-labelTreatment

Summary

This study aims to assess the therapeutic efficacy and safety of venetoclax in combination with azacitidine and CAG(VA-CAG) as induction regimen in newly diagnosed young patients with acute myeloid leukemia(AML).

Timeline

Start
2022-12-01
Primary completion
2024-12-30
Completion
2025-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Aclacinomycin Unknown 12 mg/m2
Subject Aclacinomycin Unknown 14 mg/m2
Subject Azacitidine Other / unclassified 75 mg/m2 Subcutaneous
Subject Cytarabine Small molecule 10 mg/m2 Subcutaneous
Subject Cytarabine Small molecule 3000 mg/m2 Subcutaneous
Subject Venetoclax Small molecule 400 mg Oral