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ENROLLING BY INVITATION
NCT07813390
PHASE2

Homoharringtonine, Lisaftoclax, and Azacitidine for AML After Venetoclax-Based Therapy Failure

Sponsor: Guangdong Second Provincial General Hospital

View on ClinicalTrials.gov

Summary

Venetoclax (Ven) resistance is common in the treatment of acute myeloid leukemia (AML). Patients with Ven resistance have poor response and survival, except those with specific targeted therapy. Whether we could use new BCL-2 inhibitors to replace Ven and combine with the agents which have been shown to enhance the antilekeumia effect of BCL-2 inhibitors, to overcome Ven resistance? This is unknown up until now. This multi-center, prospective, open-label, single-arm study will evaluate the efficacy and safety of homoharringtonine combined with lisaftoclax and azacitidine (HLA) as salvage therapy for adults with AML after failure of a Ven-containing regimen. Ven treatment failure is defined as no response after at least two consecutive cycles of a Ven-containing regimen or relapse during continued, protocol-compliant Ven-based therapy after a prior response. The study plans to enroll 73 participants. The primary endpoint is the overall response rate after two treatment cycles. Secondary endpoints include complete remission (CR), CR with incomplete blood count recovery (CRi), measurable residual disease (MRD) negativity, survival and relapse, and treatment-related adverse events.

Official title: A Multi-Center, Prospective, Open-Label, Single-Arm Study of Homoharringtonine Combined With Lisaftoclax and Azacitidine in Patients With Acute Myeloid Leukemia After Failure of Venetoclax-Based Therapy

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

73

Start Date

2026-09-01

Completion Date

2028-08-31

Last Updated

2026-09-10

Healthy Volunteers

No

Interventions

DRUG

Lisaftoclax (APG-2575)

Lisaftoclax will be administered orally on Days 1-14 of each 28-day cycle: 200 mg on Day 1, 400 mg on Day 2, and 600 mg once daily on Days 3-14. If concomitant use of a CYP3A4 inhibitor is required, the protocol specifies a reduced lisaftoclax dose of 200-400 mg/day according to the instruction.

DRUG

homoharringtonine

Homoharringtonine will be administered at 1 mg/m\^2 by intravenous infusion once daily on Days 1-7 of each 28-day cycle.

DRUG

Azacitidine (AZA)

Azacitidine will be administered at 75 mg/m\^2 by subcutaneous injection once daily on Days 1-7 of each 28-day cycle.

Locations (1)

Guangdong Second Provincial General Hospital

Guangzhou, Guangdong, China