Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**YH001 + envafolimab** is a combination of two antibody-based immunotherapies, investigated for the treatment of advanced or metastatic sarcoma. YH001 is an IgG1 monoclonal antibody that targets CTLA-4, designed to enhance anti-tumor immune responses through T cell activation and regulatory T cell depletion. It displays enhanced antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) compared to ipilimumab in preclinical studies. Envafolimab (KN035) is a humanized single-domain antibody against PD-L1, forming a fusion protein with a mutated IgG1 Fc fragment, engineered for subcutaneous administration. Envafolimab inhibits PD-L1-mediated immune suppression, promoting T cell activation against tumor cells. Envafolimab is approved in China for MSI-H/dMMR advanced solid tumors and has demonstrated efficacy and safety in clinical trials of various cancers. The combination of YH001 and envafolimab is being studied in a multicenter Phase 1/2 trial for advanced or metastatic sarcoma, including alveolar soft part sarcoma, chondrosarcoma, leiomyosarcoma, and dedifferentiated liposarcoma[1][3][5].
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 YH001 + envafolimab.