The Medical Letter on Drugs and Therapeutics
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1344
Aztreonam for Inhalation Solution (Cayston) for Cystic Fibrosis
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The antibiotic aztreonam is now available as an inhalation solution (Cayston – Gilead) to improve respiratory symptoms in cystic fibrosis (CF) patients ≥7 years old colonized with Pseudomonas aeruginosa. It is the second inhaled antibiotic to be FDA-approved for this indication in CF patients; the aminoglycoside tobramycin (Tobi) was the first. Inhaled antibiotics offer the advantage of high airway concentrations while minimizing systemic side effects.1

CLINICAL STUDIES — In a double-blind trial, 211 CF patients were randomized to inhalation of aztreonam 75 mg or placebo for 28 days. The primary endpoint, which was the time to a need for additional inhaled or intravenous antipseudomonal antibiotics, was reached at 92 days with aztreonam and at 71 days with placebo. The prespecifed secondary outcomes of lung function and respiratory symptoms also improved ... more      

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Title: Aztreonam for Inhalation Solution (Cayston) for Cystic Fibrosis
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