Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination regimen consisting of a PD-1 antibody (commonly tislelizumab), chidamide, lenalidomide, and etoposide. It is being investigated primarily for the treatment of relapsed or refractory extranodal natural killer/T-cell lymphoma, nasal type (r/r-ENKTL). The regimen leverages multiple mechanisms: - **PD-1 antibody** (e.g., tislelizumab) acts as an immune checkpoint inhibitor by blocking the programmed death 1 receptor on T cells, thereby enhancing anti-tumor immune responses. - **Chidamide** is a selective histone deacetylase inhibitor that modulates gene expression and can induce tumor cell apoptosis while also enhancing cytotoxic T cell and NK cell activity. - **Lenalidomide** is an immunomodulatory agent that augments immune-mediated anti-tumor effects and has direct anti-proliferative properties. - **Etoposide** is a chemotherapeutic agent that inhibits topoisomerase II, leading to DNA damage in rapidly dividing cells. Clinical studies have shown promising response rates with this combination in r/r ENKTL patients who have failed prior therapies. The safety profile includes manageable hematologic toxicities such as leukopenia and anemia[6][9][2].
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 PD-1 antibody + chidamide + lenalidomide + etoposide.