AP-301 is under clinical development by Shanghai Alebund Pharmaceuticals and currently in Phase I for Hyperphosphatemia. According to GlobalData, Phase I drugs for Hyperphosphatemia have an 82% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how AP-301’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.

AP-301 overview

VS-505 is under development for the treatment of hyperphosphatemia with chronic kidney disease. The therapeutic candidate is phosphate (Pi) binder derived from gum Arabic. It is administered through oral route as capsule.

Shanghai Alebund Pharmaceuticals overview

Shanghai Alebund Pharmaceuticals., is a biopharmaceutical company dedicated to developing innovative therapies for the treatment of renal diseases and related chronic conditions. The company is headquartered Hong Kong Special Administrative Region of

For a complete picture of AP-301’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.