Setting-up an Ebola vaccine trial in a remote area of the Democratic Republic of the Congo: Challenges, mitigations, and lessons learned.

Challenges Democratic Republic of the Congo Ebola virus disease Endemic Experiences Health care providers Lessons learned Mitigations Past activities Vaccine trial

Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
31 05 2022
Historique:
received: 21 01 2022
revised: 27 04 2022
accepted: 28 04 2022
pubmed: 14 5 2022
medline: 27 5 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

Since the largest Ebola outbreak in West Africa (2013-2016) highlighted the potential threat of the Ebola virus to the world, several vaccines have been under development by different pharmaceutical companies. To obtain vaccine licensure, vaccine trials assessing the safety, immunogenicity and efficacy of new vaccines among different populations (e.g. different in age, gender, race, and ethnicity) play a crucial role. However, while this deadly disease mainly affects Central and West Africa, clinical trial regulations are becoming increasingly complex and consequently more expensive, influencing the affected low- and middle-income countries (LMICs) in performing high quality clinical trials. Consequently, the completion of such trials in LMICs takes more time and vaccines and drugs take longer to be licensed. To overcome some of the obstacles faced, the EBOVAC3 consortium, funded by the European Union's Innovative Medicines Initiative and the Coalition for Epidemic Preparedness Innovations, enabled high quality vaccine trials in Central and West Africa through extensive North-South collaborations. In this article, the encountered challenges, mitigations, recommendations and lessons learned from setting-up an Ebola vaccine trial in a remote area of the Democratic Republic of Congo are presented. These challenges are grouped into eight categories: (1) Regulatory, political and ethical, (2) Trial documents, (3) International collaborations, (4) Local trial staff, (5) Community engagement and sensitization, (6) Logistics, (7) Remoteness and climate conditions, (8) Financial. By sharing the encountered challenges, implemented mitigations and lessons learned for each of these categories, we hope to prepare and inform other researchers aspiring a well-functioning clinical trial unit in similar remote settings in LMICs. ClinicalTrials.gov identifier: NCT04186000.

Identifiants

pubmed: 35550847
pii: S0264-410X(22)00544-8
doi: 10.1016/j.vaccine.2022.04.094
pii:
doi:

Substances chimiques

Ebola Vaccines 0

Banques de données

ClinicalTrials.gov
['NCT04186000']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3470-3480

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Trésor Zola Matuvanga (T)

Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo; Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium; Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium.

Ynke Larivière (Y)

Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium; Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium. Electronic address: ynke.lariviere@uantwerpen.be.

Gwen Lemey (G)

Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium; Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium.

Jessie De Bie (J)

Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium; Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium.

Solange Milolo (S)

Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo.

Rachel Meta (R)

Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo.

Emmanuel Esanga (E)

Tshuapa Provincial Health Division, The Democratic Republic of the Congo.

Paul Peter Vermeiren (PP)

Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium; Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium.

Séverine Thys (S)

Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium; Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium.

Jean-Pierre Van Geertruyden (JP)

Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium.

Pierre Van Damme (P)

Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.

Vivi Maketa (V)

Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo.

Junior Matangila (J)

Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo.

Patrick Mitashi (P)

Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo.

Hypolite Muhindo-Mavoko (H)

Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo.

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