EBO-BOOST

Summary
The Ebola Virus Disease (EVD) remains a significant deadly threat with severe societal implications. There are currently two approved vaccines for Ebola prevention for which the duration of their protection remains uncertain. Given the periodic outbreaks in West and Central Africa, particularly in the Democratic Republic of the Congo (DRC), the need for revaccination arises. However, questions linger regarding the timing and method of revaccination, including the safety and efficacy of combining different vaccine types.
The aim of our study is to:
Facilitate the rapid deployment of vaccines during outbreaks.
Determine the efficacy and safety of combinations for booster shots and establishing clear guidelines for revaccination protocols.
Investigate factors for why certain individuals do not respond well to vaccines.
Strengthen local capacity for future epidemics through facilitating in-country testing infrastructure.
Funding
Coalition of Epidemic Preparedness Innovations (CEPI)
Merck Sharp & Dohme (MSD)
Directorate-General for Development Cooperation and Humanitarian Aid (DGD)
Project
Safety and immunogenicity of Ervebo® and Zabdeno® booster vaccines against Ebola Virus following previous vaccination with the Zabdeno/Mvabea® or Ervebo® vaccine schedules in DRC: a mix-and-match phase II RCT
Period
October 2023 – March 2027
Contact
Dr Wim Adriaensen
Principal Investigator
✉ wadriaensen@itg.be
Selien Oostvogels
Study Coordinator
✉ soostvogels@itg.be
Partners
Research units
Clinical Immunology
Tropical Laboratory Medicine Research Group
Clinical Trial Unit
Clinical Tropical Medicine Research Group

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