Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Takeda Gets Japan Approval for Low-Dose Form of Ninlaro
Takeda Pharmaceutical said on August 16 that it has earned Japanese regulatory approval for an additional 0.5 mg capsule version of its multiple myeloma (MM) drug Ninlaro (ixazomib). The new version, which comes on top of the existing 2.3 mg,…
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