Loading...
Loading...
Genzyme,
a Sanofi company
SNY, announced today that it
has received a Complete Response Letter from the U.S. Food and Drug
Administration (FDA) for its supplemental Biologics License Application
seeking approval of Lemtrada (alemtuzumab) for the treatment of
relapsing forms of multiple sclerosis.
See full press release© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in