Eisai files for full FDA approval for Alzheimer's drug Leqembi
Jan 6 (Reuters) - Japanese drugmaker Eisai Co Ltd (4523.T) said on Saturday it had submitted an application to the U.S. Food and Drug Administration for a standard review of its Alzheimer's drug Leqembi, which was recently approved under the agency's accelerated review process.
Reporting by Bhanvi Satija in Bengaluru; Editing by William Mallard
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