Japan is considering a new approach to its “special” market expansion re-pricing that would exclude drug sales tied to private…
BUSINESS
EMA Delays Decision on Leqembi Due to Procedural Issues
Eisai said on March 22 that the regulatory review of its Alzheimer’s disease drug lecanemab by a key European Medicines Agency (EMA) panel has been postponed due to procedural reasons. The deliberation process of lecanemab was delayed because the EMA…
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