Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tisotumab vedotin + bevacizumab is a combination investigational cancer therapy composed of **tisotumab vedotin**, an antibody-drug conjugate targeting tissue factor, and **bevacizumab**, a monoclonal antibody targeting vascular endothelial growth factor A (VEGF-A). Tisotumab vedotin delivers a cytotoxic payload (monomethyl auristatin E) directly to tissue factor-expressing cancer cells, causing cell death, while bevacizumab inhibits angiogenesis by preventing VEGF-A from binding its receptors on endothelial cells. This combination is under clinical investigation primarily for recurrent or metastatic cervical cancer, with studies demonstrating a manageable safety profile and promising antitumor activity[1][5][7]. Tisotumab vedotin was developed by Genmab and Seagen; bevacizumab was developed by Genentech/Roche.
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 tisotumab vedotin + bevacizumab.