Clinical Trials Directory

Trials / Completed

CompletedNCT01159561

Western Equine Encephalitis Vaccine, Inactivated

Phase 1 Study to Evaluate the Safety and Immunogenicity of the Western Equine Encephalitis (WEE) Vaccine, Inactivated, TSI-GSD 210, Lot 3-1-92, In Healthy Adults

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
U.S. Army Medical Research and Development Command · Federal
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This study is designed to determine the safety and immunogenicity of WEE Vaccine Lot number 3-1-92.

Detailed description

Study Objectives: Primary: To assess safety of the Western Equine Encephalitis (WEE) Vaccine, Inactivated, TSI-GSD 210, lot 3-1-92. Secondary: To evaluate immunogenicity of the Western Equine Encephalitis (WEE) Vaccine, Inactivated, TSI-GSD 210, lot 3-1-92.

Conditions

Interventions

TypeNameDescription
BIOLOGICALWestern Equine Encephalitis VaccineSubject will be vaccinated with 0.5 mL of reconstituted WEE vaccine, inactivated, TSI-GSD 210 (Lot 3-1-92) subcutaneously in the upper outer aspect of the deltoid region.

Timeline

Start date
2010-02-01
Primary completion
2011-08-01
Completion
2012-03-01
First posted
2010-07-09
Last updated
2019-04-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01159561. Inclusion in this directory is not an endorsement.

Western Equine Encephalitis Vaccine, Inactivated (NCT01159561) · Clinical Trials Directory