GM-60106 is under clinical development by JD Bioscience and currently in Phase I for Metabolic Dysfunction-Associated Steatohepatitis (MASH). According to GlobalData, Phase I drugs for Metabolic Dysfunction-Associated Steatohepatitis (MASH) have a 71% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how GM-60106’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.
GM-60106 overview
GM-60106 is under development for the treatment of metabolic dysfunction-associated steatohepatitis (non-alcohol related steatohepatitis or MASH or NASH), fibrosis and obesity. It is administered orally and acts by targeting 5-hydroxytryptami,ne receptor 2A (HTR2A).
JD Bioscience overview
JD Bioscience focuses on small molecule-based novel drug development. JD Bioscience is headquartered in Gwangju, South Korea.
For a complete picture of GM-60106’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
