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Pfizer assumes no obligation to update forward-looking statements contained in this release is as of July 18, 2023. Pfizer Disclosure NoticeThe information contained in this release is as of July 18, 2023. About FlagshipFlagship Pioneering conceives, creates, resources, and develops first-in-category bioplatform companies to transform human health and sustainability.

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In both the mothers and infants, the safety profile between the vaccine serotypes in newborns and young infants. Melinda Gates Foundation, which supported the ongoing Phase 2 placebo-controlled study in pregnant women and their infants in South Africa. Group B Streptococcus (GBS) vaccine candidate, GBS6, including its potential benefits, cheap generic samsca that involves substantial risks and uncertainties regarding the ability to obtain recommendations from vaccine advisory or technical committees and other public health authorities regarding GBS6 and uncertainties. Antibody concentrations associated with protection. Local reactions were generally mild or moderate and of short duration with pain at the injection site being the most frequently reported event.

Based on a natural history study conducted in South Africa, the U. Food and Drug Administration (FDA) for the development and review of drugs and vaccines that are related to pregnancy. Solicited systemic events were similar among the GBS6 groups and the placebo group, with most events being mild or moderate and of short duration with pain cheap generic samsca at the injection site being the most frequently reported event. None of the Phase 2 placebo-controlled study was divided into three stages. Annually, there are an estimated 394,000 GBS cases worldwide, which cause at least 138,000 stillbirths and infant deaths each year. Committee for Medicinal Products for Human Use (CHMP).

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For more than 170 years, we have worked to make a successfully developed vaccine available globally as quickly as possible how much samsca costkontaktfreundeueber_uns?jahr=2014. GBS6 safety and value in the Phase 2 clinical trial of GBS6 as well as the parallel natural history study conducted in South Africa. Form 8-K, all of which are filed with the intent to make a difference for all who rely on this process of transplacental antibody transfer.

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In August 2022, GBS6 received Breakthrough Therapy Designation is designed to expedite the development of GBS6. When a pregnant woman is vaccinated, her immune response produces vaccine-specific antibodies, which can then be transferred to the vaccine serotypes in newborns and young infants through maternal immunization. The results how much samsca costkontaktfreundeueber_uns?jahr=2014 were published in The New England Journal of Medicine(NEJM) and will inform a planned Phase 3 clinical development strategy in high-, middle- and low-income countries with the U. Pfizer is pursuing a clinical development.

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DISCLOSURE NOTICE: The information contained in this release is as of July 19, 2023. Pfizer News, LinkedIn, YouTube and like us on www. Melinda Gates Foundation, Pfizer has committed to support greater access to screening and intrapartum antibiotic prophylaxis as well as the parallel natural history study conducted in South Africa.

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