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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

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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

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 29 Oct 2024

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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

    • Most Recent Events

    • 26 Oct 2024 Planned End Date changed from 1 Jan 2026 to 8 Jan 2026.
    • 26 Oct 2024 Status changed from not yet recruiting to recruiting.
    • 01 Oct 2024 New trial record

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