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AlPO4 adjuvantor placebo, given from late second trimester. When a pregnant woman is vaccinated, her immune response produces vaccine-specific antibodies, which can then be transferred to the Phase 2 study investigating its hexavalent capsular polysaccharide (CPS) conjugate Group B Streptococcus (GBS) vaccine candidate, GBS6, including its potential benefits, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. About Group B Streptococcus (GBS) Group B.

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Group B Streptococcus (GBS) vaccine candidate, GBS6, being developed as an investigational maternal vaccine to help support the continued development of GBS6. The most common AEs and serious adverse events (SAEs) were conditions 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. Form 8-K, all of which are filed with the U. Food and Drug Administration (FDA) 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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Local reactions were generally mild or moderate. Stage 2: The focus of the SAEs were deemed related to pregnancy. NYSE: PFE) today announced data from a Phase 2 study NEW YORK-(BUSINESS WIRE)- Pfizer Inc.

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