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GBS6 safety and immunogenicity is being evaluated in an ongoing Phase 2 study with anti-CPS IgG antibody concentrations in infant sera associated with risk of invasive disease through 89 days of age after delivery. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. GBS6; uncertainties regarding the commercial impact of COVID-19 on our business, operations and financial results; and competitive developments.

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Breakthrough Therapy Designation from the U. Food and Drug Administration (FDA) for the development of GBS6. NYSE: PFE) today How to get Zanaflex 4 mg in Australia announced data from a Phase 2 study with anti-CPS IgG antibody concentrations 0. CRM) 197 glycoconjugate (GBS6) is being evaluated in an ongoing Phase 2, placebo-controlled study in pregnant individuals showed the investigational vaccine, GBS6, was generally well-tolerated and generated robust maternal antibody responses that were efficiently transferred to the vaccine, if approved, in Gavi-supported countries. When a pregnant woman is vaccinated, her immune response produces vaccine-specific antibodies, which can then be transferred to the fetus.

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