Study of VA Combined With HAAG Regimen in Newly Diagnosed Intermediate and High-risk AML Patients

PHASE2RecruitingINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

February 15, 2024

Primary Completion Date

May 30, 2026

Study Completion Date

December 30, 2026

Conditions
Intermediate Risk Acute Myeloid LeukemiaHigh Risk Acute Myeloid Leukemia
Interventions
DRUG

venetoclax, azacitidine and HAAG regimen

Venetoclax:100mg, qd, d1;200mg, qd, d2;400 mg, qd, d3\~10, per os; Azacitidine:75mg/m2/d, d1\~7, subcutaneous injection; Homoharringtonine:1mg/d, d4\~10, intravenous infusion; Aclarubicin:10mg/d, d4\~7, intravenous infusion; Cytarabine:10mg/m2,q12h,d4\~10, subcutaneous injection; Granulocyte colony-stimulating factor (G-CSF): 50-300μg/d (when WBC counts are less than 20×10\^9/L ),subcutaneous injection;

Trial Locations (1)

215006

RECRUITING

The First Affiliated Hospital of Soochow University, Suzhou

All Listed Sponsors
lead

The First Affiliated Hospital of Soochow University

OTHER