Japan’s largest drugmaker Takeda Pharmaceutical (TYO: 4502) today announced new data from a Phase III study of Entyvio (vedolizumab) for the treatment of adults with moderately to severely active ulcerative colitis (UC) and Crohn’s disease (CD).
Data from the ongoing open-label extension study of GEMINI LTS (Long-Term Safety) will be released as oral presentations during the 21st United European Gastroenterology Week (UEGW) in Vienna, Austria.
Two of the abstracts demonstrate that the efficacy observed in vedolizumab Phase III induction and maintenance trials of 52 weeks was maintained over the course of an additional 52 weeks of open label follow up.
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