Clinical trial

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

NCT00366782 · National Institute of Allergy and Infectious Diseases (NIAID), NIH · Completed

Key facts

NCT number NCT00366782
Title Safety of and Immune Response to a Cow/Human Parainfluenza Virus Vaccine (rB/HPIV3) in Healthy Infants, Children, and Adults
Official title A Phase 1 Study of the Safety and Immunogenicity of the Recombinant Live-Attenuated Chimeric Bovine/Human Parainfluenza Type 3 Virus Vaccine, rB/HPIV3, Lot PIV3 #101A, Delivered as Nose Drops to Adults 18 to 49 Years of Age, HPIV3-Seropositive Children 15 to 59 Months of Age, and HPIV3-Seronegative…
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 rB/HPIV3, Placebo
Enrollment 51
Start date Mar 1, 2007
Primary completion Feb 1, 2011
Completion Jun 1, 2011
First posted Aug 21, 2006
Last update posted Mar 1, 2012
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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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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