Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The HVA regimen is a triple combination therapy developed by Nanfang Hospital, Southern Medical University, for the treatment of acute myeloid leukemia (AML). The regimen consists of homoharringtonine (HHT), venetoclax (VEN), and azacitidine (AZA). Homoharringtonine is a plant-derived alkaloid that inhibits protein synthesis by binding to the ribosomal A-site, thereby preventing the initial step of protein translation. Venetoclax is a selective small-molecule inhibitor of B-cell lymphoma 2 (BCL-2), an anti-apoptotic protein frequently overexpressed in AML cells, which promotes programmed cell death. Azacitidine is a hypomethylating agent that acts as a DNA methyltransferase inhibitor, leading to the reactivation of tumor suppressor genes and induction of cell differentiation. This combination is designed to synergistically target multiple survival and resistance pathways in leukemic cells. It is currently being evaluated in a Phase 3 clinical trial for newly diagnosed high-risk AML patients, comparing its efficacy and safety against standard intensive chemotherapy or the venetoclax-azacitidine doublet.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on homoharringtonine + venetoclax + azacitidine.