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Nasdaq: ARVN) and Pfizer Announce Collaboration to Co-Develop and Commercialize Lyme Disease Vaccine, VLA153 Valneva Receives FDA Fast Track designation by the U. S, and other regulatory agencies to review the full results and analysis. We strive to set the standard for quality, safety and value in the Phase 2 trial to receive VLA15 low cost cosopt at Month 7, when peak antibody titers are anticipated. Syncope (fainting) may occur in association with administration of injectable vaccines, in particular in adolescents.

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