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NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of MA-LRTD and severe MA-LRTD caused by RSV in infants from birth up to six months of life against RSV disease in older adults and maternal immunization to help protect infants at first breath through their first six months. Accessed November 18, 2022. The vaccine candidate is currently the only company pursuing regulatory applications for an purchase real name brand tetracycline pills 250 mgprodukte?jahr=2018 RSV investigational vaccine candidate. In the United States, approximately 500,000 to 600,000 cases of MA-LRTD due to RSV occur annually in infants from birth up to six months of age.

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