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Phase 1 Study to Evaluate the Safety, Tolerability, and Immunogenicity of Hantaan and Puumala Virus DNA Vaccines, pWRG/HTN-M(x) and pWRG/PUU-M(s2), for Prevention of Hemorrhagic Fever With Renal Syndrome Administered to Healthy Adult Volunteers Using the TDS-IM Electroporation Delivery Device.

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Phase 1 Study to Evaluate the Safety, Tolerability, and Immunogenicity of Hantaan and Puumala Virus DNA Vaccines, pWRG/HTN-M(x) and pWRG/PUU-M(s2), for Prevention of Hemorrhagic Fever With Renal Syndrome Administered to Healthy Adult Volunteers Using the TDS-IM Electroporation Delivery Device.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 13 Dec 2024

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At a glance

  • Drugs PWRG-HTN-M(co) (Primary) ; PWRG-HTN-M(co)/pWRG-PUUV-M(s2) (Primary)
  • Indications Hantaan virus infections; Puumala virus infections; Viral haemorrhagic fevers
  • Focus Adverse reactions

    • Most Recent Events

    • 10 Dec 2024 According to the PharmaJet Media Release, the results from this trial published in Nature.
    • 01 Jan 2013 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 27 Aug 2012 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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