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项与 RSV/hMPV/PIV3 vaccine(Sanofi Pasteur) 相关的临床试验A Phase 1, Dose-Escalation, Randomized, Active-Controlled, Modified Double-Blind, Parallel-Group, Multi-Arm Study to Investigate the Safety and Immunogenicity of a Combined Respiratory Syncytial Virus/Human Metapneumovirus/Parainfluenza Virus Type 3 Vaccine Candidate in Adult Participants Aged 60 Years and Older
The purpose of this phase 1 study is to evaluate whether the vaccine is safe and can help the body to develop germ fighting agents called "antibodies" (immunogenicity) against the respiratory syncytial virus (RSV), human metapneumovirus (hMPV), and parainfluenza virus type 3 (PIV3). The study will use different doses of PIV3 only and different combinations of RSV/hMPV/PIV3 or RSV/hMPV or only RSV vaccine in adults aged 60 years and older.
100 项与 RSV/hMPV/PIV3 vaccine(Sanofi Pasteur) 相关的临床结果
100 项与 RSV/hMPV/PIV3 vaccine(Sanofi Pasteur) 相关的转化医学
100 项与 RSV/hMPV/PIV3 vaccine(Sanofi Pasteur) 相关的专利(医药)
100 项与 RSV/hMPV/PIV3 vaccine(Sanofi Pasteur) 相关的药物交易