Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
In a Turnaround, EU Panel Backs Takeda’s Ninlaro for Conditional Approval
Takeda Pharmaceutical said on September 20 that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) recommended “conditional approval” for its multiple myeloma (MM) drug Ninlaro (ixazomib). The panel had nixed its approval earlier this year.…
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