Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CAHAG is an experimental combination chemotherapy regimen being investigated for the treatment of relapsed or refractory acute myeloid leukemia (AML). Developed by The First Affiliated Hospital of Soochow University, the regimen utilizes a "double epigenetic priming" strategy by combining two epigenetic modifiers—chidamide (a histone deacetylase inhibitor) and azacitidine (a hypomethylating agent)—with a chemotherapy backbone known as the HAG regimen. The HAG component in this specific protocol consists of homoharringtonine, low-dose cytarabine, and granulocyte colony-stimulating factor (G-CSF). G-CSF is used to prime dormant leukemia cells, inducing them into the cell cycle to increase their sensitivity to the cytotoxic effects of cytarabine and homoharringtonine. This multi-drug approach aims to overcome chemoresistance by modulating the epigenetic landscape and enhancing the pro-apoptotic signals in malignant cells. Chidamide is provided for these clinical trials by Shenzhen Chipscreen Biosciences.
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 CAHAG regimen.