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项与 Quadrivalent Influenza mRNA Vaccine(Sanofi Pasteur) 相关的临床试验A Phase I/II Study to Investigate the Safety and Immunogenicity of Quadrivalent Influenza mRNA Vaccines MRT5421, MRT5424, and MRT5429 in Healthy Participants Aged 18 Years and Above
The purpose of this study is to evaluate the safety and immunogenicity of a single intramuscular (IM) injection of different formulations of Quadrivalent Influenza Vaccine (QIV) messenger ribonucleic acid (mRNA) (MRT5421, MRT5424, and MRT5429) compared to an active control (QIV- standard dose (SD), QIV- high dose (HD) [adults ≥ 65 years of age only], or quadrivalent recombinant influenza vaccine (RIV4)) in adults 18 years of age and older.
Sanofi Pasteur Quadrivalent Intradermal Influenza Vaccine Pregnancy Registry Protocol
The Sanofi Pasteur Fluzone Intradermal Quadrivalent vaccine (Fluzone QIV-ID) Pregnancy Registry will be a prospectively recruited pregnancy surveillance program designed to collect to collect and analyze information on vaccine exposures, pregnancy outcomes, and fetal and offspring outcomes on pregnant women exposed to Fluzone QIV-ID vaccine.
Sanofi Pasteur Quadrivalent Influenza Vaccine Pregnancy Registry Protocol
The Sanofi Pasteur Quadrivalent Influenza Vaccine (QIV) Pregnancy Registry will be a prospectively recruited pregnancy surveillance program designed to collect and analyze information on vaccine exposures, pregnancy outcomes, and fetal and offspring outcomes.
100 项与 Quadrivalent Influenza mRNA Vaccine(Sanofi Pasteur) 相关的临床结果
100 项与 Quadrivalent Influenza mRNA Vaccine(Sanofi Pasteur) 相关的转化医学
100 项与 Quadrivalent Influenza mRNA Vaccine(Sanofi Pasteur) 相关的专利(医药)
100 项与 Quadrivalent Influenza mRNA Vaccine(Sanofi Pasteur) 相关的药物交易