XW-004 is under clinical development by Sciwind Biosciences and currently in Phase I for Type 2 Diabetes. According to GlobalData, Phase I drugs for Type 2 Diabetes have a 64% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how XW-004’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.
XW-004 overview
XW-004 is under development for the treatment of nonalcoholic steatohepatitis (NASH), obesity and type 2 diabetes. It is administered through oral route. The drug candidate acts by targeting glucagon like peptide 1 receptor (GLP1R). The drug candidate is being developed based on polypeptide or recombinant protein preparation platform technology.
It was also under development for the treatment of liver fibrosis.
Sciwind Biosciences overview
Sciwind Biosciences (Sciwind) is a clinical-stage biopharmaceutical company. It focuses on the discovery and development of monotherapy and combination treatments to treat metabolic diseases. The company’s pipeline products include XW003, injectable GLP-1 analogs and XW004, an oral formulation of GLP-1 peptide targets diabetes; XW014, A GLP-1R agonist; and XW003+XW0017, a GLP-1 and GIP combination for obesity; and XW010, XW013, and XW015 drug programs treats and non-alcoholic steatohepatitis (NASH). The company operates in China and the US. Sciwind is headquartered in Hangzhou, Zhejiang, China.
For a complete picture of XW-004’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.
