The FDA approves Roche (OTCQX:RHHBY +2%)
unit Genentech’s supplemental marketing application for Xofluza
(baloxavir marboxil) for the treatment of acute uncomplicated influenza
in people at least 12 years old who have been symptomatic for no more
than 48 hours and are at high risk of developing flu-related
complications.
The agency first approved the polymerase acidic
endonuclease inhibitor a year ago for the acute treatment of
uncomplicated flu in otherwise healthy people at least 12 years old who
have been symptomatic for no more than 48 hours.
https://seekingalpha.com/news/3506585-fda-oks-expanded-use-roche-flu-med-xofluza
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