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Gilead Submits New Drug Application To U.S. FDA For Aztreonam Lysine For Inhalation For Cystic Fibrosis
Cystic Fibrosis Gilead Sciences, Inc. (Nasdaq:GILD) announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for marketing approval of aztreonam lysine for inhalation (75 mg three times daily), an investigational therapy in development for people with cystic fibrosis (CF) who have pulmonary Pseudomonas aeruginosa (P. aeruginosa) infection.
