Clinical trial

A Study to Evaluate a Single Intravenous Dose of Motavizumab for the Treatment…

NCT00421304 · MedImmune LLC, Industry · Completed

Key facts

NCT number NCT00421304
Title A Study to Evaluate a Single Intravenous Dose of Motavizumab for the Treatment of Children Hospitalized With Respiratory Syncytial Virus (RSV) Illness
Official title A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate a Single Intravenous Dose of Motavizumab (MEDI-524), a Humanized Enhanced Potency Monoclonal Antibody Against Respiratory Syncytial Virus (RSV), for the Treatment of Children Hospitalized With RSV Illness
Lead sponsor MedImmune LLC, Industry
Status Completed
Study type Interventional
Conditions RSV Illness in ≤12 Months of Participants
Intervention type Biological, Other
Interventions Motavizumab, Placebo
Enrollment 118
Start date Jan 10, 2007
Primary completion Sep 17, 2009
Completion Sep 17, 2009
First posted Jan 11, 2007
Last update posted Aug 27, 2021
Countries Australia, Chile, New Zealand, Panama, United States

At a glance

  • 10–99 Study sites
  • Yes 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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