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A Phase 1b, Randomized, Observer-Blind, Placebo-Controlled, Dose Ranging Trial to Evaluate the Safety and Immunogenicity of mRNA-1653, a Combined Human Metapneumovirus (hMPV) and Parainfluenza Virus Type 3 (PIV3) Vaccine When Administered to Adults, and to Children 12 to 59 Months of Age With Serologic Evidence of Prior Exposure

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A Phase 1b, Randomized, Observer-Blind, Placebo-Controlled, Dose Ranging Trial to Evaluate the Safety and Immunogenicity of mRNA-1653, a Combined Human Metapneumovirus (hMPV) and Parainfluenza Virus Type 3 (PIV3) Vaccine When Administered to Adults, and to Children 12 to 59 Months of Age With Serologic Evidence of Prior Exposure

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Feb 2024

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At a glance

  • Drugs MRNA-1653 (Primary)
  • Indications Metapneumovirus infections; Parainfluenza virus infections
  • Focus Adverse reactions
  • Sponsors Moderna Therapeutics

    • Most Recent Events

    • 02 Feb 2023 Status changed from active, no longer recruiting to completed.
    • 22 Sep 2022 Status changed from recruiting to active, no longer recruiting.
    • 16 Dec 2021 Planned number of patients changed from 75 to 59.

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