Clinical trial

Safety Study of a Monoclonal Antibody to Respiratory Syncytial Virus (RSV) in…

NCT00192504 · MedImmune LLC, Industry · Completed

Key facts

NCT number NCT00192504
Title Safety Study of a Monoclonal Antibody to Respiratory Syncytial Virus (RSV) in Children Hospitalized With RSV Infection
Official title A Phase 1, Randomized, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of a Single Intravenous Dose of MEDI-524, a Humanized Enhanced Potency Monoclonal Antibody to Respiratory Syncytial Virus (RSV), in Otherwise Healthy Children…
Lead sponsor MedImmune LLC, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Respiratory Syncytial Virus Prophylaxis
Intervention type Biological, Other
Interventions Motavizumab, Placebo
Enrollment 31
Start date Mar 1, 2004
Primary completion Jan 1, 2005
Completion Jan 1, 2005
First posted Sep 19, 2005
Last update posted Oct 8, 2021

At a glance

  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies