VE-818 by Vedanta Biosciences for Graft Versus Host Disease (GVHD): Likelihood of Approval

VE-818 is under clinical development by Vedanta Biosciences and currently in Phase I for Graft Versus Host Disease (GVHD). According to GlobalData, Phase I drugs for Graft Versus Host Disease (GVHD) have an 89% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how VE-818’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

VE-818 overview

VE-818 is under development for the treatment of graft versus host disease (GVHD). It is administered through oral route as capsule. The therapeutic candidate comprises of consortia of immune-modulating microbiome-derived bacteria.

Vedanta Biosciences overview

Vedanta Biosciences is a clinical-stage company which focuses on microbiome, which performs critical functions that preserve health including modulating our immune system and providing colonization resistance against infectious pathogens. Vedanta Biosciences is headquartered in Cambridge, Massachusetts, the US.

For a complete picture of VE-818’s drug-specific PTSR and LoA scores, buy the report here.