XW-014 is under clinical development by Sciwind Biosciences and currently in Phase I for Metabolic Dysfunction-Associated Steatohepatitis (MASH). According to GlobalData, Phase I drugs for Metabolic Dysfunction-Associated Steatohepatitis (MASH) does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the XW-014 LoA Report. 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.
XW-014 overview
XW-014 is under development for the treatment of non-alcoholic steatohepatitis (NASH), obesity and type 2 diabetes. The drug candidate acts by targeting glucagon like peptide 1 receptor (GLP1R). It is administered through oral route.
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 product pipeline includes XW003, injectable GLP-1 analogs; XW004, an oral formulation of GLP-1 peptide; XW014, A GLP-1R agonist; and XW003 and XW0017, a GLP-1 and GIP combination for the treatment of diabetes, obesity, and non-alcoholic steatohepatitis (NASH). Sciwind is also investigating XW010, XW013, and XW015 drug programs for undisclosed targets. The company operates a research and development center in Beijing, China. It has a presence in China and the US. Sciwind is headquartered in Hangzhou, Zhejiang, China.
For a complete picture of XW-014’s drug-specific PTSR and LoA scores, buy the report here.
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