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FDA: Specific Fast Track Designation for Subcutaneous Formulation of Leqembi for Alzheimer Disease Needed for Rolling Review
This alters the course of developer Eisai's regulatory submission plans for lecanemab in the treatment of early Alzheimer disease.
United states
Los angeles
Liua eisai
Helen lavretsky
William blair
Kansteinerf eisai
Drug administration
American college of neuropsychopharmacology
Biogen inc
American psychiatric association
Eisai co ltd
Department of psychiatry
American association for geriatric psychiatry
Fast track
Biologics license application
Psychiatric times
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