CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 4,789 enrolled
Drug / intervention
Ad26.ZEBOV +4 morebiological
Likely dose
Ad26.ZEBOV 0.5 mLfrom 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/NCT02876328
NCT02876328Phase 2Completed

Partnership for Research on Ebola VACcinations (PREVAC)

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Aug 23, 2016·Updated Jun 26, 2024

In Brief

A Phase 2 clinical trial evaluating Ad26.ZEBOV, MVA-BN-Filo, and 3 other interventions for Ebola Virus Disease. Completed, enrolled 4,789 participants across 6 sites in 4 countries.

Detailed Summary

The purpose of this study is to evaluate the safety and immunogenicity of three vaccine strategies that may prevent Ebola virus disease (EVD) events in children and adults. Participants will receive either the Ad26.ZEBOV (rHAd26) vaccine with a MVA-BN-Filo (MVA) boost, or the rVSVΔG-ZEBOV-GP (rVSV) vaccine with or without boosting, or placebo.

Study Details

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedAug 23, 2016
Enrollment StartMar 27, 2017
Primary CompletionDec 24, 2019
Study CompletionDec 20, 2023
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 9.9 years ago

Interventions

Ad26.ZEBOVbiological

0.5 mL at a dose of 5x10\^10 vp administered by intramuscular (IM) injection into the upper arm for adults or the thigh for children

MVA-BN-Filobiological

0.5 mL at a dose of 1x10\^8 InfU administered by intramuscular (IM) injection into the upper arm for adults or the thigh for children

rVSVΔG-ZEBOV-GPbiological

1 mL at a nominal dose of 2x10\^7 pfu/mL administered by intramuscular (IM) injection into the upper arm for adults or the thigh for children

Placebobiological

0.5 mL or 1 mL (depending upon the arm) sterile normal saline administered by intramuscular (IM) injection into the upper arm for adults or the thigh for children

rVSV boostbiological

1 mL at a nominal dose of 2x10\^7 pfu/mL administered by intramuscular (IM) injection into the upper arm for adults or the thigh for children