Clinical trial

Trial to Assess the Safety and Tolerability of the Liquid Formulation of CAIV-T…

NCT00192400 · MedImmune LLC, Industry · Completed

Key facts

NCT number NCT00192400
Title Trial to Assess the Safety and Tolerability of the Liquid Formulation of CAIV-T in Healthy Children.
Official title A Prospective, Randomized, Double-Blind, Placebo-Controlled Trial to Compare the Safety, Tolerability, Immunogenicity and Efficacy of One Dose and Two Doses of a Liquid Formulation of Influenza Virus Vaccine, Trivalent, Types A & B, Live Cold-Adapted (CAIV-T) Compared With Placebo in Healthy…
Lead sponsor MedImmune LLC, Industry
Collaborators Wyeth is now a wholly owned subsidiary of Pfizer Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Healthy
Intervention type Biological
Interventions CAIV-T
Enrollment 2,160
Start date Mar 1, 2002
Completion Nov 1, 2002
First posted Sep 19, 2005
Last update posted Oct 3, 2006

At a glance

  • 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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