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A Phase 1, Randomized, Rater and Subject Blinded Placebo Controlled Study to Evaluate the Safety, Reactogenicity, Tolerability and Immunogenicity of a Standard and a Fractional Dose of H1 Influenza Vaccine Delivered by VX-103 (a MIMIX Microneedle Patch (MAP) System) in Healthy Adults ≥18-39 Years of Age

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Trial Profile

A Phase 1, Randomized, Rater and Subject Blinded Placebo Controlled Study to Evaluate the Safety, Reactogenicity, Tolerability and Immunogenicity of a Standard and a Fractional Dose of H1 Influenza Vaccine Delivered by VX-103 (a MIMIX Microneedle Patch (MAP) System) in Healthy Adults ≥18-39 Years of Age

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 14 Nov 2023

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At a glance

  • Drugs VX-103 (Primary)
  • Indications Influenza virus infections
  • Focus Adverse reactions
  • Sponsors Vaxess Technologiess

    • Most Recent Events

    • 28 Aug 2023 New trial record

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