Clinical trial

Trial to Assess Safety, Tolerability, and Immunogenicity of Influenza Virus…

NCT00192270 · MedImmune LLC, Industry · Completed

Key facts

NCT number NCT00192270
Title Trial to Assess Safety, Tolerability, and Immunogenicity of Influenza Virus Vaccine, Trivalent, Types A and B, Live Cold-adapted (CAIV-T) in Healthy Children
Official title A Prospective, Open-label, Phase II, Multi-center Study of the Safety, Tolerability and Immunogenicity of Influenza Virus Vaccine, Trivalent, Types A and B, Live Cold-adapted (CAIV-T) in Healthy Children, Aged 6 to 17 Years
Acronym FluMist
Lead sponsor MedImmune LLC, Industry
Collaborators Wyeth is now a wholly owned subsidiary of Pfizer Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Healthy
Intervention type Biological
Interventions CAIV-T
Enrollment 498
Start date Oct 1, 2000
Primary completion Jan 1, 2001
Completion Jan 1, 2001
First posted Sep 19, 2005
Last update posted Mar 6, 2012
Countries Belgium, Finland

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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