GM-60106 is under clinical development by JD Bioscience and currently in Phase I for Fibrosis. According to GlobalData, Phase I drugs for Fibrosis does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the GM-60106 LoA Report. 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.

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.

This content was updated on 10 June 2024

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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.