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This entry refers to a group of experimental vaccine formulations developed by Sanofi and evaluated in a Phase 1 clinical trial (NCT05306041). The program investigated different formulations of a trivalent influenza vaccine (TIV-HA) and a combined vaccine targeting respiratory syncytial virus (RSV), human metapneumovirus (hMPV), and parainfluenza virus type 3 (PIV3). The TIV-HA component targets the hemagglutinin (HA) proteins of three influenza strains, while the multivalent respiratory vaccine targets the fusion (F) proteins of RSV, hMPV, and PIV3. These candidates utilize lipid nanoparticle (LNP) delivery technology, which is characteristic of mRNA-based vaccine platforms, designed to elicit robust immune responses against multiple major respiratory pathogens. The trial aimed to assess the safety and immunogenicity of these next-generation formulations in healthy adults aged 18-49 years.
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