FDA Grants Fast Track Designation To Aradigm Corporation’s Pulmaquin For Non-Cystic Fibrosis Bronchiectasis

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HAYWARD, Calif.--(BUSINESS WIRE)--Aradigm Corporation (Nasdaq:ARDM) (the “Company”) today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to its lead product candidate, Pulmaquin®, for treatment of non-cystic fibrosis bronchiectasis (non-CF BE) patients with chronic lung infections with Pseudomonas aeruginosa. Aradigm is currently in Phase 3 clinical trials for this indication.

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