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FDA approves weekly subcutaneous lecanemab for Alzheimer’s

First publishedJul 15, 17:32 UTC
Last updatedJul 15, 20:23 UTC · 6m ago
11 outletInvesting.com · Company News
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FDA approves weekly subcutaneous lecanemab for Alzheimer’s
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TOKYO and CAMBRIDGE, Mass. (NASDAQ:BIIB) announced today that the U.S.

Reported by 1 outlet Investing.com · Company News. See all sources ↓

TOKYO and CAMBRIDGE, Mass. (NASDAQ:BIIB) announced today that the U.S. Food and Drug Administration has approved a supplemental Biologics License Application for once-weekly lecanemab-irmb subcutaneous injection as an initiation dose for treating early Alzheimer’s disease, according to a press release statement. The approval marks a significant milestone for Eisai, a prominent player in the Pharmaceuticals industry with a market capitalization of $7.4 billion.

Read the full report at Investing.com · Company News

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In brief
What's the story?
TOKYO and CAMBRIDGE, Mass. (NASDAQ:BIIB) announced today that the U.S.
How widely is it covered?
1 outlet, average source rating 5.0/10.
When was it last updated?
6m ago.
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    FDA approves weekly subcutaneous lecanemab for Alzheimer’s

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    Investing.com · Company News
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