Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Bevacizumab + evofosfamide is an investigational combination therapy for cancer. Bevacizumab is a monoclonal antibody that inhibits vascular endothelial growth factor A (VEGF-A), thereby blocking angiogenesis and reducing tumor blood supply. Evofosfamide (also known as TH-302 or Evo) is a hypoxia-activated prodrug that releases the DNA crosslinking agent bromo-isophosphoramide mustard under low oxygen conditions typical of solid tumors. This combination has been studied primarily in patients with recurrent glioblastoma who are refractory to bevacizumab alone. The rationale for the combination is that resistance to antiangiogenic therapy like bevacizumab can increase tumor hypoxia, making tumors more susceptible to activation of evofosfamide and its cytotoxic effects[1][3][6]. Clinical trials have shown modest activity in this setting but have not led to regulatory approval[1][4][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 bevacizumab + evofosfamide.