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A Phase 1, Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1653, a Combined Human Metapneumovirus and Human Parainfluenza Virus Type 3 Vaccine, When Administered to Healthy Adults

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A Phase 1, Randomized, Observer-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1653, a Combined Human Metapneumovirus and Human Parainfluenza Virus Type 3 Vaccine, When Administered to Healthy Adults

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 10 Feb 2020

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At a glance

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

    • Most Recent Events

    • 05 Feb 2020 Status changed from active, no longer recruiting to completed.
    • 06 Dec 2019 Planned End Date changed from 1 Dec 2019 to 1 Jan 2020.
    • 02 Oct 2019 Interim results presented in the Moderna Therapeutics media release.

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