Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This drug regimen is a **combination therapy** consisting of **chidamide** (a histone deacetylase inhibitor), **decitabine** (a DNA methyltransferase inhibitor), and an **anti-PD-1 antibody** (most often camrelizumab, but the anti-PD-1 could be another agent in different studies). This triplet targets epigenetic modulation and immune checkpoint inhibition to treat various malignancies, particularly in patients who are refractory to prior anti-PD-1 or anti-PD-L1 therapy. - **Chidamide** inhibits histone deacetylase (HDAC), reprogramming tumor and immune cell gene expression, enhancing immune recognition, and making tumor cells more susceptible to immune attack. - **Decitabine** blocks DNA methyltransferase 1 (DNMT1), increasing tumor antigen expression and upregulating HLA molecules, helping restore tumor immunogenicity and potentially overcoming resistance to immune checkpoint inhibitors. - **Anti-PD-1 antibodies** (like camrelizumab) block the interaction between PD-1 and PD-L1, releasing T cells from inhibitory signaling and promoting anti-tumor immune responses. Recent clinical trials, especially in **relapsed/refractory classical Hodgkin lymphoma (cHL)**, have demonstrated that this triplet produces robust objective response rates, including in patients who had progressed on prior anti-PD-1/decitabine therapy. The regimen is being developed for patients ineligible for, or refusing, transplant in cHL, and may also be under investigation for other lymphomas and solid tumors[2][4][5][6][9][10].
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 chidamide + decitabine + anti-PD-1 antibody.