Japan is considering a new approach to its “special” market expansion re-pricing that would exclude drug sales tied to private…
BUSINESS
FDA Accepts Leqembi SC for Review; Target Date Set to Aug. 31
Eisai said on January 14 that the US FDA has accepted for regulatory review its application for a subcutaneous autoinjector version of Leqembi (lecanemab) as a weekly maintenance treatment for early Alzheimer’s disease. The target action date under the Prescription…
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