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

Conducting a vaccine trial in a low- and middle-income country (LMIC) can present unique challenges and lessons learned. This Ebola vaccine trial, enrolling 699 healthcare providers and frontliners and jointly set up by the University of Antwerp (Sponsor) and the University of Kinshasa (Principal In...

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Veröffentlicht in:Vaccine 2023-12, Vol.41 (51), p.7587-7597
Hauptverfasser: Larivière, Ynke, Matuvanga, Trésor Zola, Lemey, Gwen, Osang'ir, Bernard Isekah, Vermeiren, Paul Peter, Milolo, Solange, Meta, Rachel, Kimbulu, Primo, Esanga, Emmanuel, Matangila, Junior, Van Geertruyden, Jean-Pierre, Van Damme, Pierre, Maketa, Vivi, Muhindo-Mavoko, Hypolite, Mitashi, Patrick
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container_end_page 7597
container_issue 51
container_start_page 7587
container_title Vaccine
container_volume 41
creator Larivière, Ynke
Matuvanga, Trésor Zola
Lemey, Gwen
Osang'ir, Bernard Isekah
Vermeiren, Paul Peter
Milolo, Solange
Meta, Rachel
Kimbulu, Primo
Esanga, Emmanuel
Matangila, Junior
Van Geertruyden, Jean-Pierre
Van Damme, Pierre
Maketa, Vivi
Muhindo-Mavoko, Hypolite
Mitashi, Patrick
description Conducting a vaccine trial in a low- and middle-income country (LMIC) can present unique challenges and lessons learned. This Ebola vaccine trial, enrolling 699 healthcare providers and frontliners and jointly set up by the University of Antwerp (Sponsor) and the University of Kinshasa (Principal Investigator (PI)), was conducted in Boende, a remote city in the Democratic Republic of the Congo (DRC), between December 2019 and October 2022 (ClinicalTrials.gov: NCT04186000). While being bound by strict ICH-GCP and international funder regulations, this trial, exemplary for being a public-private partnership, required collaboration between several international stakeholders (e.g., two universities, a pharmaceutical company, and a clinical research organization), local communities and government agencies. Here we address several logistical and administrative challenges, cultural differences, language barriers and regulatory, political, and ethical considerations over the trial's 2.5-year duration, while tailoring and adapting the study to the specific local context. Lessons learned include the importance of clear communication with participants in all phases of the study, but also within the study team and among different stakeholders. Challenges, mitigations, and lessons learned are presented in nine categories (e.g., safety management; trial documentation, tools, and materials; communication, staff training and community engagement/sensitization; financial and administrative hurdles; and more). Ultimately, to reach the successful end of the vaccine trial in this remote Ebola endemic area in the DRC, careful planning, collaboration, and great flexibility and adaptability was often required from all involved partners. Despite the encountered challenges, the vaccine trial discussed in this paper was able to obtain high participant retention rates (i.e., 92% of participants completed the study). We hope that other international teams aspiring to conduct similar trials in remote areas of LMICs can learn from the way our challenges were addressed, mitigations developed, and lessons were learned.
doi_str_mv 10.1016/j.vaccine.2023.11.030
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This Ebola vaccine trial, enrolling 699 healthcare providers and frontliners and jointly set up by the University of Antwerp (Sponsor) and the University of Kinshasa (Principal Investigator (PI)), was conducted in Boende, a remote city in the Democratic Republic of the Congo (DRC), between December 2019 and October 2022 (ClinicalTrials.gov: NCT04186000). While being bound by strict ICH-GCP and international funder regulations, this trial, exemplary for being a public-private partnership, required collaboration between several international stakeholders (e.g., two universities, a pharmaceutical company, and a clinical research organization), local communities and government agencies. Here we address several logistical and administrative challenges, cultural differences, language barriers and regulatory, political, and ethical considerations over the trial's 2.5-year duration, while tailoring and adapting the study to the specific local context. 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source MEDLINE; Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects Adaptability
Algorithms
Belgium
biomedical research
Clinical trials
Clinical Trials as Topic
Collaboration
Communication
Community involvement
Community participation
Company structure
Cooperation
Corporate sponsorship
Cultural factors
Democratic Republic of the Congo
Democratic Republic of the Congo - epidemiology
Digitization
Ebola Vaccines
Ebola virus
Ebolavirus
ethics
Government agencies
health services
Hemorrhagic Fever, Ebola - epidemiology
Hemorrhagic Fever, Ebola - prevention & control
Humans
Immunization
Infectious diseases
Laboratories
Legislation
Local communities
Pharmaceutical industry
Political factors
politics
Public private partnerships
Remote regions
Safety management
stakeholders
Teams
Universities
Vaccines
title Conducting an Ebola vaccine trial in a remote area of the Democratic Republic of the Congo: Challenges, mitigations, and lessons learned
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