Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Leqembi Iqlik Now under FDA Review for Initiation Phase
Eisai said on January 26 that the US FDA has accepted an application for Leqembi Iqlik, the subcutaneous autoinjector formulation of the anti-amyloid antibody lecanemab, as a once-weekly option for the initiation-phase treatment of early Alzheimer’s disease. The filing seeks…
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