Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
BUSINESS
Takeda Pushes Back Assumed Biosimilar Entry in US by 3-5 Years
The biosimilar entry for Takeda Pharmaceutical’s inflammatory bowel disease (IBD) treatment Entyvio (vedolizumab) in the US is expected to be three to five years later than the company’s previous assumption of May 2026, according to CEO Christophe Weber. Mr Weber…
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