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A Phase I, first in human (FIH), randomised, double-blind, placebo-controlled, dose-escalation study to evaluate safety, reactogenicity and immunogenicity of the recombinant respiratory syncytial virus vaccines (BARS13) when administered intramuscularly (IM) to healthy adult volunteers

Trial Profile

A Phase I, first in human (FIH), randomised, double-blind, placebo-controlled, dose-escalation study to evaluate safety, reactogenicity and immunogenicity of the recombinant respiratory syncytial virus vaccines (BARS13) when administered intramuscularly (IM) to healthy adult volunteers

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 09 Sep 2019

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At a glance

  • Drugs Respiratory syncytial virus vaccine (Primary)
  • Indications Respiratory syncytial virus infections
  • Focus Adverse reactions; First in man
  • Most Recent Events

    • 06 Sep 2019 Status changed from active, no longer recruiting to completed.
    • 13 May 2019 Status changed from recruiting to active, no longer recruiting.
    • 23 Jan 2019 According to Australian New Zealand Clinical Trials Registry record, recruitment completion is expected on 2/19/2019.
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