SNP-610 is under clinical development by Sinew Pharma and currently in Phase II for Metabolic Dysfunction-Associated Steatohepatitis (MASH). According to GlobalData, Phase II drugs for Metabolic Dysfunction-Associated Steatohepatitis (MASH) have a 25% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how SNP-610’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
SNP-610 overview
SNP-610 is under development for the treatment of metabolic dysfunction-associated steatohepatitis (MASH). It is administered through the oral route as a tablet. The drug candidate acts by targeting diacylglycerol O-acyltransferase 1 (DGAT1), hormone-sensitive lipase and CYP2E1 enzymes. It is a first-in-class drug candidate.
Sinew Pharma overview
Sinew Pharma is a Taiwan-based company mainly engaged in the development and research of new drugs. The Company primarily focus on the research and development of liver disease treatment drugs and pain medication. The Company’s main products include f
For a complete picture of SNP-610’s drug-specific PTSR and LoA scores, buy the report here.
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