XO/URAT1 Dual Inhibitor is under clinical development by BioSeedin and currently in Phase I for Hyperuricemia. According to GlobalData, Phase I drugs for Hyperuricemia have a 90% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how XO/URAT1 Dual Inhibitor’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.
XO/URAT1 Dual Inhibitor overview
The drug candidate is under development for the treatment of hyperuricemia. It is a small molecule, xanthine oxidase (XO) and urate transporter 1 (URAT1) dual inhibitor and is administered through oral route.
BioSeedin overview
BioSeedin, a subsidiary of Acrobiosystems Co., Ltd, is a financial advisory firm engaged in offering advisory, asset management and public relations services. The company is headquartered in Beijing City, Beijing, China.
For a complete picture of XO/URAT1 Dual Inhibitor’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.
