Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
EMA Initiates Review of Oral MS Treatment Gilenya Following Reports of Heart Problems
The European Medicines Agency (EMA) announced on January 20 that it has initiated a review to evaluate the benefits and risks of the oral multiple sclerosis treatment Gilenya (fingolimod) in the wake of reports of heart problems in patients taking…
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REGULATORY
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