VAC Regimen for AML Patients Who Failed to Response to VA Regimen

PHASE2RecruitingINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

February 1, 2024

Primary Completion Date

December 1, 2026

Study Completion Date

December 1, 2026

Conditions
Acute Myeloid Leukemia
Interventions
DRUG

chidamide in combination with venetoclax and azacitidine (VAC)

Enrolled patients were given chidamide 10 mg every day on days 1-14, azacitidine 75mg/m2 every day on days 1-7, and oral venetoclax began at 100mg on day 1 and increased stepwise over 3 days to reach the target dose of 400mg (100mg, 200mg, and 400mg) on days 1-28. Dose adjustments for concomitant venetoclax with CYP3A4 inhibitors were made according to the literature.

Trial Locations (1)

215006

RECRUITING

The First Affiliated Hospital of Soochow University, Suzhou

All Listed Sponsors
collaborator

Jining Medical University

OTHER

collaborator

The Second People's Hospital of Huai'an

OTHER

collaborator

The First Affiliated Hospital of Bengbu Medical University

OTHER

collaborator

Northern Jiangsu People's Hospital

OTHER

collaborator

Affiliated Hospital of Nantong University

OTHER

lead

The First Affiliated Hospital of Soochow University

OTHER