Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Keytruda Gets Label Update to Add Adjuvant Data for Melanoma
The Pharmaceuticals and Medical Devices Agency (PMDA) on September 26 announced a label update for MSD’s PD-1 inhibitor Keytruda (pembrolizumab), which added new data from a global PIII study that tested the drug as an adjuvant therapy for certain melanoma…
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REGULATORY
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Japan’s pharmaceutical industry is undergoing a structural shift in its workforce, with the role of sales reps shrinking while production…
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…
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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…