Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
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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 is ramping up its push to spread regional formularies nationwide, a policy expected to standardize treatments, strengthen supply resilience,…
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…
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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The Japanese government approved a bill to amend the Pharmaceuticals and Medical Devices (PMD) Act at its Cabinet meeting on…
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…