ECC-4703 is under clinical development by Eccogene (Shanghai) 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 ECC-4703’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.
ECC-4703 overview
The drug candidate is under development for the treatment of dyslipidemia and non-alcoholic steatohepatitis (NASH). It is a novel small molecule acts by targeting thyroid hormone receptor beta (THRB). It is administered through oral route.
Eccogene (Shanghai) overview
Eccogene (Shanghai) is a biopharmaceutical company dedicated to providing innovative therapeutic solutions to address unmet medical needs globally. It is headquartered in Shanghai, China.
For a complete picture of ECC-4703’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.
