CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 1,500 enrolled
Drug / intervention
VSVG-ZEBOV +2 morebiological
Likely dose
Not stated in 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/NCT02344407
NCT02344407Phase 2Completed

Partnership for Research on Ebola Vaccines in Liberia (PREVAIL)

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Jan 26, 2015·Updated Apr 8, 2021

In Brief

A Phase 2 clinical trial evaluating VSVG-ZEBOV, ChAd3-EBO Z, and 1 other intervention for Ebola Virus. Completed, enrolled 1,500 participants across 1 site.

Detailed Summary

Background: \- Ebola virus disease (EVD) affects many people in Liberia and other countries in West Africa. It is caused by the Ebola virus and makes people sick with fever, headache, vomiting, diarrhea, rash, and bleeding. About half the people with EVD die. There is no approved treatment for it. Researchers are studying two Ebola vaccines. The vaccines do not cause Ebola. Objectives: \- To study the safety and efficacy of two Ebola vaccines. Eligibility: \- Adults 18 and older who live in Liberia and are at risk for Ebola infection but have never had Ebola. Design: * Participants will give information including birthdate, gender, occupation, and location of home. They will give contact information for themselves and 2 alternate contacts. They will give a history of their contact with people with Ebola. Some participants may have a physical. They may have blood taken. * Participants will be injected with either an Ebola vaccine or a placebo with a needle in the upper arm. The placebo is a salt solution. * Participants will have blood taken. * Participants will be watched for 30 minutes. * Participants will return to the clinic 1 week and 1 month after they get the shot. They will have blood taken. * After that, participants will be contacted monthly to discuss how they are feeling. They may be contacted by phone, may visit the clinic, or may have a home visit. * The study ends 8-12 months after participants get the shot. If one of the vaccines works against Ebola and does not have many side effects, participants can get the vaccine if they did not get it in the study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsEbola Virus
CountriesLiberia
Collaborators--

Timeline

Phase 2CompletedFinished
201520162017201820192020202120222023202420252026
First PostedJan 26, 2015
Enrollment StartJan 20, 2015
Primary CompletionJun 1, 2016
Study CompletionNov 1, 2020
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 11.4 years ago

Interventions

VSVG-ZEBOVbiological

The VSVdeltaG-ZEBOV vaccine is comprised of a single recombinant (vesicular stomatitis virus) VSV isolate (11481 nt) modified to replace the gene encoding the G envelope glycoprotein with the gene encoding the envelope glycoprotein from the Ebola virus Zaire strain (ZEBOV)

ChAd3-EBO Zbiological

The ChAd3-EBO Z vaccine is comprised of a ChAd3 vector with a DNA fragment insert that encodes the Ebola virus glycoprotein, which is expressed on the virion surface and is critical for attachment to host cells and catalysis of membrane fusion.

Placebobiological