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Clinical Trials associated with Hexavalent Influenza mRNA Vaccine(Sanofi Pasteur) / Active, not recruitingPhase 1/2 A Phase I/II, Randomized, Modified Double-blind Study to Investigate the Safety and Immunogenicity of Different Doses of Hexavalent Influenza mRNA HA + mRNA NA Vaccine in Adult Participants 50 Years of Age and Older
The purpose of this study is to evaluate the safety and immunogenicity of a single intramuscular injection of different formulations of a hexavalent influenza messenger ribonucleic acid (mRNA) vaccine composed of differing dose levels of trivalent (TIV) mRNA hemagglutinin (HA) in combination with TIV mRNA-neuraminidase (NA) compared to an active control ((Fluzone standard-dose quadrivalent influenza vaccine (QIV-SD) or Fluzone high-dose quadrivalent influenza vaccine (QIV-HD) in adults 50 years of age and older.
100 Clinical Results associated with Hexavalent Influenza mRNA Vaccine(Sanofi Pasteur)
100 Translational Medicine associated with Hexavalent Influenza mRNA Vaccine(Sanofi Pasteur)
100 Patents (Medical) associated with Hexavalent Influenza mRNA Vaccine(Sanofi Pasteur)
100 Deals associated with Hexavalent Influenza mRNA Vaccine(Sanofi Pasteur)