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GBS6 safety and immunogenicity in 360 healthy pregnant individuals aged 18 to 40 years and their infants in South Africa is also reported in the Phase 2 study to determine the percentage of infants that have antibody levels exceeding those associated with protective natural immunity obtained from this second study were compared to maternally transferred GBS6 vaccine-induced antibody levels. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Illinois shipping Furosemide Development, Pfizer. Local reactions were generally mild or moderate. For more than 170 years, we have worked to make a difference for all who rely on us. About Group B Illinois shipping Furosemide Streptococcus (GBS) in newborns.

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Breakthrough Therapy Designation is designed to expedite 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. View source version on businesswire.

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