Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Vilastobart + atezolizumab is an investigational combination therapy comprising vilastobart (formerly XTX101), a tumor-activated, Fc-enhanced anti-CTLA-4 monoclonal antibody, and atezolizumab, a monoclonal antibody targeting PD-L1 (Tecentriq). Vilastobart is engineered to remain inactive systemically and become activated by proteases in the tumor microenvironment, where it blocks CTLA-4, leading to immune checkpoint inhibition and selective depletion of CTLA-4 high regulatory T cells through Fc receptor engagement and antibody-dependent cell-mediated cytotoxicity (ADCC). Atezolizumab blocks PD-L1, preventing it from binding PD-1 and B7-1, thereby releasing additional brakes on anti-tumor T cell activity. The combination is specifically being investigated in metastatic microsatellite stable colorectal cancer (MSS CRC) and other advanced solid tumors, with aims to improve efficacy and reduce immune-related toxicities compared to traditional anti-CTLA-4 therapies[2][3][4][6][7].
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 vilastobart + atezolizumab.