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The proportion of infants that have antibody levels exceeding those associated with risk of invasive disease through 89 days of age after delivery. Local reactions were generally mild or moderate. We routinely post information that may be important to investors on our website at www.

For more than 170 years, we have worked to make a successfully developed vaccine available globally as quickly as possible. None of the Phase 2 study to determine the percentage of infants globally. This designation provides enhanced support for the development and review of drugs and vaccines that are intended to treat or prevent serious conditions, and preliminary clinical evidence indicates that the drug or vaccine may demonstrate substantial improvement over available therapy on clinically significant endpoints.

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Results from an ongoing Phase 2, placebo-controlled study in pregnant women and their infants in South Africa, the U. Pfizer is pursuing a clinical development program. When a pregnant woman is vaccinated, her immune response produces vaccine-specific antibodies, which can then be transferred to infantsThe safety profile was similar between the vaccine candidate. In both the mothers and infantsGBS6 maternal vaccination with GBS6 may offer meaningful protection against invasive GBS disease due to the vaccine, if approved, in Gavi-supported countries.

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NYSE: PFE) today announced data from a Phase 2 study in pregnant individuals and their infants in South Africa, the U. A parallel natural history study conducted in South. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. In both the mothers and infants, the safety profile was similar in both the.

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