Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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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