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Home » MEDIMMUNE RECEIVES COMPLETE RESPONSE LETTER FROM FDA FOR NEW FLUMIST FORMULATION
MEDIMMUNE RECEIVES COMPLETE RESPONSE LETTER FROM FDA FOR NEW FLUMIST FORMULATION
MedImmune Inc. announced that it received complete response letter from the U.S. Food and Drug Administration for a supplemental biologics license application related to the new formulation of FluMist, the intranasal flu vaccine. MedImmune is seeking approval to use refrigerator-stable CAIV-T - cold adapted influenza vaccine trivalent, in preventing influenza in healthy individuals aged 5 to 49 years. Trading Markets (http://www.tradingmarkets.com/tm.site/news/BREAKING%20NEWS/308986/)
KEYWORDS FDAnews Drug Daily Bulletin
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