Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Disitamab vedotin + sintilimab + multimodality radiotherapy is a combination therapeutic regimen being investigated for the treatment of HER2-positive advanced gastric cancer. The regimen consists of disitamab vedotin (RC48), a novel antibody-drug conjugate (ADC) targeting HER2 with a monomethyl auristatin E (MMAE) payload; sintilimab, a programmed cell death protein 1 (PD-1) monoclonal antibody; and multimodality radiotherapy (MMRT), which combines low-dose radiotherapy (LDRT) and stereotactic body radiotherapy (SBRT). The rationale for this combination is based on the potential of disitamab vedotin to modulate the tumor immune microenvironment and synergize with PD-1 blockade, while MMRT enhances systemic anti-tumor responses by releasing tumor antigens and further remodeling the immune microenvironment. This approach is specifically targeted at patients who have failed standard first- and second-line therapies.
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 + sintilimab + multimodality radiotherapy.