Study to Evaluate MEDI-534 in Healthy Adults

NCT00111878 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2007-07-03

No results posted yet for this study

Summary

The primary objective of this study is to describe the safety and tolerability of a single dose of MEDI-534 when administered to healthy adult volunteers.

Conditions

  • Respiratory Syncytial Virus Infections
  • Parainfluenza Infections

Interventions

DRUG

MEDI-534

Sponsors & Collaborators

  • MedImmune LLC

    lead INDUSTRY

Principal Investigators

  • Margarita Gomez, MD · MedImmune LLC

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-04-30
Completion
2005-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00111878 on ClinicalTrials.gov