drugset / Trial / NCT02564523

Safety, Tolerability and Immunogenicity Study of 3 Prime-boost Regimens for Ebola Vaccines Ad26.ZEBOV/MVA-BN-Filo in Healthy Adults, Children and Human Immunodeficiency Virus Positive (HIV+) Adults

NCT02564523

RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to assess the safety, tolerability and immunogenicity of three heterologous prime-boost regimens for Ebola vaccines Ad26.ZEBOV and MVA-BN-Filo. The study will include healthy adults and elderly participants, HIV infected participants and healthy children in 2 age strata.

Timeline

Start
2015-11-06
Primary completion
2019-02-12
Completion
2019-02-12

Publications

Drugs

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