Phase I Study to Determine the Safety, Infectivity, and Tolerability of 2 Doses of Live Attenuated Recombinant Cold-Passaged (cp) 45 Human Parainfluenza Type 3 Virus Vaccine, rHPIV3cp45, Lot PIV3 102A, Delivered as Nose Drops to HPIV3-Seronegative Infants and Children 6 to 36 Months of Age, at a 6 Month Interval.

Trial Profile

Phase I Study to Determine the Safety, Infectivity, and Tolerability of 2 Doses of Live Attenuated Recombinant Cold-Passaged (cp) 45 Human Parainfluenza Type 3 Virus Vaccine, rHPIV3cp45, Lot PIV3 102A, Delivered as Nose Drops to HPIV3-Seronegative Infants and Children 6 to 36 Months of Age, at a 6 Month Interval.

Completed
Phase of Trial: Phase I

Latest Information Update: 02 Jan 2013

At a glance

  • Drugs MEDI 560 (Primary)
  • Indications Parainfluenza virus infections
  • Focus Adverse reactions; Pharmacodynamics
  • Most Recent Events

    • 02 Jan 2013 Actual end date Dec 2011 added as reported by ClinicalTrials.gov.
    • 01 Feb 2012 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
    • 25 Dec 2009 New trial record
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