drugset / Trial / NCT02313077

A Safety and Immunogenicity Study of Heterologous Prime-Boost Ebola Vaccine Regimens in Healthy Participants

NCT02313077

Phase 1 Completed 87 enrolled Crucell Holland BV
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to test the safety and immunogenicity of MVA-BN-Filo and Ad26.ZEBOV as heterologous prime-boost vaccine regimens in healthy adult participants.

Timeline

Start
2014-12-17
Primary completion
2015-04-17
Completion
2016-03-15

Drugs

EvaluationDrugModalityDoseRoute
Subject ADENOVIRUS TYPE 26 ENCODING EBOLA VIRUS GLYCOPROTEIN Vaccine 5e+10 unknown Intramuscular
Subject MVA-BN-Filo Vaccine 1e+08 unknown Intramuscular

Indications

No indication recorded.