Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
1st Line Use, Administration Interval Will Be Key Differentiator for Keytruda: MSD Japan Chief
MSD’s anti-PD-1 antibody Keytruda (pembrolizumab) can set itself apart from its archrival Opdivo (nivolumab) with its first-line use and once-every-three-weeks dosing for the treatment of PD-L1-positive unresectable, advanced or relapsed non-small cell lung cancer (NSCLC), the company’s Japan President Jannie…
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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 FY2026 drug pricing reform is set to usher in a new phase for the generics market, effectively bringing an…
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…