Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
US FDA Approves Additional CIDP Use for Takeda’s Gammagard Liquid
Takeda Pharmaceutical said on January 29 that the US FDA has approved a label expansion of Gammagard Liquid as an intravenous immunoglobulin therapy to improve neuromuscular disability and impairment in adults with chronic inflammatory demyelinating polyneuropathy (CIDP). With the approval,…
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