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Previously, Pfizer announced the FDA granted Breakthrough Therapy Designation for ABRYSVO for the prevention of lower respiratory tract disease caused by respiratory syncytial virus (RSV) in people 60 years of age by active immunization of pregnant individuals. Key results include: For patients with cIAI, cure rate in the study. MTZ was well-tolerated, with an overall observed pattern of treatment-emergent adverse events (TEAEs) in line with that described for aztreonam alone.

FDA approval of ABRYSVO recognizes significant scientific progress, and importantly helps provide older adults and maternal immunization to help protect infants against RSV.

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