Clinical trial

Study of MEDI-524 (Motavizumab) for the Prophylaxis of Serious Respiratory…

NCT00129766 · MedImmune LLC, Industry · Completed

Key facts

NCT number NCT00129766
Title Study of MEDI-524 (Motavizumab) for the Prophylaxis of Serious Respiratory Syncytial Virus (RSV) Disease in High-Risk Children
Official title A Pivotal Phase 3 Study of MEDI-524 (Numax; Motavizumab), an Enhanced Potency Humanized RSV Monoclonal Antibody, for the Prophylaxis of Serious RSV Disease in High-Risk Children
Lead sponsor MedImmune LLC, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Respiratory Syncytial Virus Infections
Intervention type Biological
Interventions motavizumab (MEDI-524), palivizumab
Enrollment 6,635
Start date Nov 1, 2004
Primary completion May 1, 2006
Completion May 1, 2006
First posted Aug 12, 2005
Last update posted Aug 28, 2013
Countries Argentina, Australia, Austria, Brazil, Bulgaria, Canada, Chile, Czechia, Denmark, France, Germany, Greece and 12 more

At a glance

  • 100–999 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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