Takeda files BLA for vedolizumab for Crohn's and ulcerative colitis in USA

21 June 2013

The US subsidiary of Japan’s largest drugmaker Takeda Pharmaceutical (TYO: 4502) has submitted a Biologics License Application (BLA) with the US Food and Drug Administration for vedolizumab, an investigational humanized monoclonal antibody for the treatment of adults with moderately to severely active Crohn's disease (CD) and ulcerative colitis (UC), the two most common types of inflammatory bowel disease (IBD). A similar filing was made earlier this year in Europe (The Pharma Letter March 8).

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