Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Takeda Wins Approval for Liquid Kenketu Glovenin-I 10%; Overseas-Derived Version Already Launched
Takeda Pharmaceutical said on February 10 that it has received Japanese regulatory approval for Kenketu Glovenin-I 10% for IV Injection (polyethylene glycol-treated human immunoglobulin), a plasma-derived therapy. The product is an improved liquid formulation of the existing freeze-dried Kenketu Glovenin-I…
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