Clinical trial

Safety of and Immune Response to a Human Parainfluenza Virus Vaccine…

NCT00308412 · National Institute of Allergy and Infectious Diseases (NIAID), NIH · Completed

Key facts

NCT number NCT00308412
Title Safety of and Immune Response to a Human Parainfluenza Virus Vaccine (rHPIV3cp45) in Healthy Infants
Official title Phase 1 Study to Determine the Safety, Infectivity, and Tolerability of Two Doses of Live Attenuated Recombinant Cold Passaged (cp) 45 Parainfluenza Type 3 Virus Vaccine, rHPIV3cp45, Lot PIV3 102A, Delivered as Nose Drops to Infants 6 to 12 Months of Age, and to HPIV3 Seronegative Infants and…
Lead sponsor National Institute of Allergy and Infectious Diseases (NIAID), NIH
Collaborators Johns Hopkins Bloomberg School of Public Health
Status Completed
Phase Phase 1
Study type Interventional
Conditions Paramyxoviridae Infections, Virus Diseases
Intervention type Biological
Interventions rHPIV3cp45, Placebo
Enrollment 45
Start date Jun 1, 2006
Primary completion Apr 1, 2010
Completion Apr 1, 2010
First posted Mar 29, 2006
Last update posted Jul 16, 2010
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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