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In December 2022, Pfizer announced that the available data support the efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including primary analysis results from the pivotal Phase 3 clinical trial (NCT05035212) RENOIR (RSV vaccine Efficacy study iN Older adults Immunized against RSV disease). Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook.

The virus can affect the lungs and breathing passages of an infected individual and can potentially cause severe illness in young infants, older adults, and individuals with certain chronic medical conditions. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative how to get strattera without a doctor?jahr=2003 medicines and vaccines. After this important discovery, Pfizer tested numerous versions of a stabilized prefusion F from subgroups A and B. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives.

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