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VE800 is an investigational **oral live biotherapeutic product** from **Vedanta Biosciences** composed of a rationally defined consortium of **11 clonal human commensal bacterial strains**. It was developed as a **microbiome-based immuno-oncology therapy** intended to modulate the gut microbiome and enhance **T-cell-mediated anti-tumor immunity**, thereby potentiating the activity of **PD-1 checkpoint blockade** such as nivolumab. Publicly described clinical development focused on **advanced or metastatic cancers**, where VE800 was evaluated in combination with Bristol Myers Squibb's Opdivo in a Phase 1 study; the study's Stage 1 response rates did not meet prespecified criteria for further expansion, and the collaboration/program was subsequently paused or discontinued.
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