Ecnoglutide is under clinical development by Sciwind Biosciences and currently in Phase II for Obesity. According to GlobalData, Phase II drugs for Obesity have a 29% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Ecnoglutide’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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-003 is under development for the treatment of non-alcoholic steatohepatitis (NASH), obesity, type 2 diabetes mellitus and liver fibrosis. It is developed based on the platform for the preparation of polypeptide and recombinant protein. It is administered injection through subcutaneous route. The drug candidate acts by targeting glucagon like peptide 1 receptor (GLP1R).
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 Ecnoglutide’s drug-specific PTSR and LoA scores, buy the report here.