HSP-638 is under clinical development by Zhejiang Boyiao Biopharmaceutical and currently in Phase I for Graves’ Ophthalmopathy. According to GlobalData, Phase I drugs for Graves’ Ophthalmopathy have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how HSP-638’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.
HSP-638 overview
HSP-638 is under development for the treatment of thyroid eye disease (Graves ophthalmopathy). The drug candidate is administered by intravenous route.
Zhejiang Boyiao Biopharmaceutical overview
Zhejiang Boyiao Biopharmaceutical is a biopharmaceutical company engaged in research, development, production and marketing of novel medicines in the areas of cerebral infarction, high uric acid, anti-pain, prenatal, postnatal care and others. The company is headquartered in Hangzhou, Zhejiang, China.
For a complete picture of HSP-638’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.
