Eisai Co., Ltd. confirmed late on 27 September that it has initiated a rolling biologics license application (BLA) submission for its anti-amyloid-beta protofibril antibody lecanemab (BAN2401) ahead of Phase III data expected in 2022, finally resolving a question opened by the US Food and Drug Administration accelerated approval of it and Biogen, Inc.’s amyloid-clearing antibody Aduhelm (aducanumab) for Alzheimer’s disease.
Aduhelm was approved in June under the subpart H pathway based on its ability to clear amyloid plaques from the...






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