Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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Takeda Resubmits NDA for DPP-4 Inhibitor in the US
Takeda Pharmaceutical announced on July 26 that its wholly-owned US subsidiary Takeda Global Research & Development Center, Inc. (TGRD) resubmitted on July 25 NDAs for the DPP-4 (dipeptidyl peptidase-4) inhibitor alogliptin (SYR-322) and the fixed-dose combination alogliptin/pioglitazone with additional data…
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Japan’s health ministry doled out regulatory approvals for a throng of new medicines on December 27 including Eli Lilly’s obesity…
Japan’s all-important reimbursement policy panel on December 20 approved an outline of drug pricing reforms for FY2024, which enshrines a…