Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Japan’s 1st Eylea Biosimilar Approval on Horizon? JAN Now Decided
The first biosimilar version of the age-related macular degeneration treatment Eylea (aflibercept) might be nearing the finish line in the regulatory review in Japan, with its Japanese non-proprietary name, or JAN, now determined. On March 22, the Ministry of Health,…
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