CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 479 enrolled
Drug / intervention
ChimeriVax-WN02 vaccine +3 morebiological
Likely dose
Placebo 0.9%from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00746798
NCT00746798Phase 2Completed

Randomized, Modified, Double-blind, Placebo-controlled, Phase II, Dose-ranging Study of the Safety and Immunogenicity of Single Dose ChimeriVax-WN02 Vaccine in Healthy Adults.

Sanofi Pasteur, a Sanofi Company·interventional·Posted Sep 4, 2008·Updated Apr 3, 2015

In Brief

A Phase 2 clinical trial evaluating ChimeriVax-WN02 vaccine and Placebo for West Nile Fever. Completed, enrolled 479 participants across 15 sites.

Detailed Summary

The purpose of this study is to determine if ChimeriVax West Nile vaccine is safe and effective in preventing West Nile disease in adults over 50 years of age.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsWest Nile Fever
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedSep 4, 2008
Enrollment StartOct 1, 2008
Primary CompletionJun 1, 2009
Study CompletionDec 1, 2009
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 17.8 years ago

Interventions

ChimeriVax-WN02 vaccinebiological

low dose, approximately 4 x 3log10, given one time subcutaneously

ChimeriVax-WN02 vaccinebiological

medium dose, approximately 4 x 4log10, given one time

ChimeriVax-WN02 vaccinebiological

high dose, approximately 4 x 5log10, given one time subcutaneously

Placebobiological

0.9%Normal Saline for Injection, given one time subcutaneously