MET-3 is under clinical development by Nubiyota and currently in Phase II for Hypertriglyceridemia. According to GlobalData, Phase II drugs for Hypertriglyceridemia have a 52% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how MET-3’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.
MET-3 overview
MET-3 is under development for the treatment of hypertriglyceridemia. It comprises live microbiota that normally reside in the human gut of a healthy individual. It is administered through oral route as a lyophilized capsule. The drug candidate is being developed based on Microbial Ecosystem Therapeutics (MET) technology.
It was also under development for obesity.
Nubiyota overview
Nubiyota operates within the pharmaceuticals and healthcare industry, specifically focusing on the therapy area of gastrointestinal disorders, with a specialization in ulcerative colitis, a type of inflammatory bowel disease. The company is headquartered in Pearl River, New York, the US.
For a complete picture of MET-3’s drug-specific PTSR and LoA scores, buy the report here.
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