Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The HVAG regimen is a combination therapy consisting of homoharringtonine (HHT), venetoclax (VEN), azacitidine (AZA), and granulocyte colony-stimulating factor (G-CSF). This regimen is being investigated by the Shanghai Jiao Tong University School of Medicine as a first-line treatment for newly diagnosed elderly patients with acute myeloid leukemia (AML) who are ineligible for intensive chemotherapy. Homoharringtonine is a plant alkaloid that inhibits protein synthesis by binding to the ribosomal A-site, thereby preventing the elongation phase of translation. Venetoclax is a selective B-cell lymphoma 2 (BCL-2) inhibitor that promotes apoptosis in leukemia cells by displacing pro-apoptotic proteins. Azacitidine is a hypomethylating agent that incorporates into DNA and RNA, inhibiting DNA methyltransferases and leading to the reactivation of tumor suppressor genes. G-CSF is included to stimulate granulocyte production and potentially sensitize leukemic blasts to the cytotoxic effects of the other agents. The combination aims to exploit synergistic effects, particularly between HHT and venetoclax, which has been shown to reduce the expression of anti-apoptotic proteins like BCL-XL and MCL-1.
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 + G-CSF.