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
Latest Information Update: 01 Oct 2024
At a glance
- Drugs RSV/hMPV/PIV3 vaccine Sanofi (Primary)
- Indications Metapneumovirus infections; Parainfluenza virus infections; Respiratory syncytial virus infections
- Focus Adverse reactions
- Sponsors Sanofi Pasteur
- 01 Oct 2024 New trial record