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Gilead Sciences, Inc. announced that the Committee for Medicinal Products for Human Use, the scientific committee of the European Medicines Agency, has adopted a negative opinion on the company's Marketing Authorisation Application for aztreonam lysine 75 mg powder and solvent for nebuliser solution in the European Union. Aztreonam lysine is an investigational therapy in development for people with cystic fibrosis who have pulmonary Pseudomonas aeruginosa infection.

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