Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
FDA Grants Priority Review Status to Multiple Myeloma Drug Ixazomib: Takeda
Takeda Pharmaceutical said on September 9 that the US FDA has granted priority review status to its novel oral proteasome inhibitor ixazomib (development code: MLN9708), which is being developed as a successor to Velcade (bortezomib).The agent, discovered by its US-based…
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In the complex landscape of the Japanese pharmaceutical market, the “status quo” is often the safest harbor. But for leaders like Kennet Brysting, former president of Gilead Japan, the status quo is the most dangerous place to stay.Innovation in Japan…
Japan’s Central Social Insurance Medical Council (Chuikyo) on November 5 approved the reimbursement listing for a slate of new medicines,…
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Japan’s all-important reimbursement policy panel on December 20 approved an outline of drug pricing reforms for FY2024, which enshrines a…