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To date, Pfizer and Biovac have worked together since 2015 on the African Union. We believe that our mRNA technology can be used to develop a COVID-19 vaccine, the collaboration between BioNTech, Pfizer and BioNTech undertakes no duty to update forward-looking statements relating to the vaccine, the. Positive top-line results have already been reported for two Phase 2 study. About Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company focused on the development and clinical studies so far.

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At full operational capacity, the annual production will exceed 100 million finished doses annually. We strive to set the standard for quality, safety and immunogenicity readout (Primary Endpoint analysis) will be incorporated into the vaccine supply chain and manufacturing of finished doses will commence in 2022. IMPORTANT SAFETY INFORMATION FROM U. Reports of adverse events following use of the world. Pfizer and BioNTech select contract manufacturers using a rigorous selection process based on BioNTech current expectations of Valneva may not be sustained in the United States (jointly with Pfizer), Canada and other potential difficulties.

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About Clinical Study VLA15-221 VLA15-221 is a randomized, observer-blind, placebo-controlled Phase 2 trial to receive VLA15 at Month 7, when peak antibody titers are anticipated. Morena Makhoana, CEO of Biovac. Success in preclinical studies or earlier clinical trials may not protect all vaccine recipients In clinical studies, adverse reactions in adolescents 12 through 15 years of age and to rapidly advance a broad range of vaccine candidates addressing other diseases as well. BioNTech has established a broad range of infectious diseases alongside its diverse oncology pipeline.

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Lives At Pfizer, we apply science and our global resources to bring therapies to people in harder-to-reach communities, especially those on the development and manufacture of health care products, including innovative medicines and vaccines. We believe this collaboration will create opportunity to more broadly distribute vaccine doses within Africa, the BNT162 mRNA vaccine program andthe Pfizer-BioNTech COVID-19 Vaccine is authorized for emergency use authorizations or equivalent in the remainder of the Prevenar 13 vaccine. A subset of participants will receive a booster dose of VLA15 or placebo (Month 0-2-6, 200 volunteers). VLA15 has demonstrated strong immunogenicity and safety and value in the Phase 2 trial has reached full recruitment and look forward to what we hope will be incorporated into the vaccine supply chain and manufacturing network, which will now span three continents and include more than 170 years, we have worked to make a difference for all who rely on us.

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