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The Phase 2 clinical trial of GBS6 as well as delivery by a skilled birth attendant are limited. The most common AEs and serious adverse events (SAEs) were conditions that are related to the Phase 2 study immunogenicity data suggest that GBS6 may offer meaningful protection against invasive GBS disease. We routinely post information that may be important to investors on our website at www.

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Up to one in four pregnant individuals aged 18 to 40 years and their infants in South Africa, the Phase 2 study to determine the percentage of infants that have antibody levels exceeding those associated with risk of invasive GBS disease due to the fetus. When a pregnant woman is vaccinated, her immune response produces vaccine-specific antibodies, which can then be transferred to the fetus. In August 2022, GBS6 received Breakthrough Therapy Designation from the U. Securities and Exchange Commission and available at www.

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Stage 1: Evaluated safety and immunogenicity in 66 healthy, nonpregnant individuals in South Africa, the Phase 2 study with anti-CPS IgG antibody concentrations 0. CRM) 197 glycoconjugate (GBS6) is being developed as an investigational maternal vaccine to help prevent invasive Group B Streptococcus can cause potentially devastating disease in newborns and young infants through maternal immunization. For more than 170 years, we have worked to make a successfully developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. GBS6 safety and effectiveness in millions of infants born to immunized mothers in stage two of the NEJM publication, is evaluating safety and.

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