Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination regimen is a chemo-immunotherapy backbone being evaluated for the treatment of frail patients with newly diagnosed classical Hodgkin lymphoma (cHL) who are ineligible for standard anthracycline-based treatments. The regimen integrates the PD-1 inhibitor pembrolizumab with a chemotherapy cocktail consisting of gemcitabine, the CD30-targeted antibody-drug conjugate brentuximab vedotin, and the alkylating agent dacarbazine. Pembrolizumab works by blocking the PD-1/PD-L1 pathway, thereby reinvigorating the immune system's T-cells to attack malignant Reed-Sternberg cells. Brentuximab vedotin provides targeted delivery of the microtubule-disrupting agent monomethyl auristatin E (MMAE) to CD30-expressing cells. Gemcitabine and dacarbazine provide additional systemic cytotoxicity by inhibiting DNA synthesis and inducing DNA damage, respectively. This study is primarily led by City of Hope Medical Center.
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 pembrolizumab + gemcitabine + brentuximab vedotin + dacarbazine.