Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Disitamab Vedotin + Tislelizumab is a combination therapy consisting of an antibody-drug conjugate (Disitamab Vedotin) and a PD-1 inhibitor (Tislelizumab). Disitamab Vedotin (RC48-ADC) is a humanized anti-HER2 antibody conjugated with monomethyl auristatin E (MMAE) via a cleavable peptide linker. It works through multiple mechanisms including MMAE-mediated direct cytotoxicity, bystander effect, and immunogenic cell death. Tislelizumab is a PD-1 inhibitor that enhances immune response against cancer cells. The combination has shown promising efficacy in urothelial carcinoma, particularly in patients with HER2 expression, with objective response rates ranging from 62.5% to 83.3% in various studies.
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 disitamab vedotin + tislelizumab.