Setting-up an Ebola vaccine trial in a remote area of the Democratic Republic of the Congo: Challenges, mitigations, and lessons learned
•Clinical trial regulations are becoming increasingly complex and demanding for low- and middle-income countries (LMICs)•International collaboration based on equal partnership can help LMICs perform high quality vaccine trials.•Maintaining acquired capacity while conducting clinical trials in LMICs...
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Published in | Vaccine Vol. 40; no. 25; pp. 3470 - 3480 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
31.05.2022
Elsevier Limited |
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Abstract | •Clinical trial regulations are becoming increasingly complex and demanding for low- and middle-income countries (LMICs)•International collaboration based on equal partnership can help LMICs perform high quality vaccine trials.•Maintaining acquired capacity while conducting clinical trials in LMICs is key and needs long term international support.•Transparency of lessons learned during clinical trials can assist for a more efficient conduct of trials.•This article describes the challenges, mitigations and lessons learned during the setup of a vaccine trial in a LMIC.
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. |
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AbstractList | •Clinical trial regulations are becoming increasingly complex and demanding for low- and middle-income countries (LMICs)•International collaboration based on equal partnership can help LMICs perform high quality vaccine trials.•Maintaining acquired capacity while conducting clinical trials in LMICs is key and needs long term international support.•Transparency of lessons learned during clinical trials can assist for a more efficient conduct of trials.•This article describes the challenges, mitigations and lessons learned during the setup of a vaccine trial in a LMIC.
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. 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. |
Author | Muhindo-Mavoko, Hypolite Vermeiren, Paul Peter Van geertruyden, Jean-Pierre De Bie, Jessie Milolo, Solange Larivière, Ynke Lemey, Gwen Mitashi, Patrick Matangila, Junior Zola Matuvanga, Trésor Van Damme, Pierre Meta, Rachel Esanga, Emmanuel Thys, Séverine Maketa, Vivi |
Author_xml | – sequence: 1 givenname: Trésor surname: Zola Matuvanga fullname: Zola Matuvanga, Trésor organization: Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo – sequence: 2 givenname: Ynke orcidid: 0000-0002-5422-0194 surname: Larivière fullname: Larivière, Ynke email: ynke.lariviere@uantwerpen.be organization: Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium – sequence: 3 givenname: Gwen surname: Lemey fullname: Lemey, Gwen organization: Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium – sequence: 4 givenname: Jessie surname: De Bie fullname: De Bie, Jessie organization: Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium – sequence: 5 givenname: Solange orcidid: 0000-0003-2507-4041 surname: Milolo fullname: Milolo, Solange organization: Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo – sequence: 6 givenname: Rachel surname: Meta fullname: Meta, Rachel organization: Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo – sequence: 7 givenname: Emmanuel surname: Esanga fullname: Esanga, Emmanuel organization: Tshuapa Provincial Health Division, The Democratic Republic of the Congo – sequence: 8 givenname: Paul Peter surname: Vermeiren fullname: Vermeiren, Paul Peter organization: Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium – sequence: 9 givenname: Séverine surname: Thys fullname: Thys, Séverine organization: Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium – sequence: 10 givenname: Jean-Pierre surname: Van geertruyden fullname: Van geertruyden, Jean-Pierre organization: Global Health Institute, Department of Family Medicine and Population Health, University of Antwerp, Wilrijk, Belgium – sequence: 11 givenname: Pierre surname: Van Damme fullname: Van Damme, Pierre organization: Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium – sequence: 12 givenname: Vivi surname: Maketa fullname: Maketa, Vivi organization: Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo – sequence: 13 givenname: Junior surname: Matangila fullname: Matangila, Junior organization: Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo – sequence: 14 givenname: Patrick surname: Mitashi fullname: Mitashi, Patrick organization: Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo – sequence: 15 givenname: Hypolite surname: Muhindo-Mavoko fullname: Muhindo-Mavoko, Hypolite organization: Tropical Medicine Department, University of Kinshasa, Kinshasa, The Democratic Republic of the Congo |
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Keywords | Lessons learned Challenges Mitigations Experiences Health care providers Democratic Republic of the Congo Vaccine trial Past activities Endemic Ebola virus disease |
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SubjectTerms | Challenges Climatic conditions Clinical trials Clinical Trials as Topic Community involvement Community participation Consortia COVID-19 Democratic Republic of the Congo Democratic Republic of the Congo - epidemiology Disease Outbreaks - prevention & control Drug dosages Ebola Vaccines Ebola virus Ebola virus disease Ebolavirus Endemic Epidemics Ethics Experiences Health care providers Hemorrhagic Fever, Ebola - epidemiology Hemorrhagic Fever, Ebola - prevention & control Humans Immunogenicity Infectious diseases Internet access Lessons learned Logistics Mitigations Mortality Past activities Pharmaceutical industry Presidential elections Vaccine trial Vaccines Viral diseases |
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Title | Setting-up an Ebola vaccine trial in a remote area of the Democratic Republic of the Congo: Challenges, mitigations, and lessons learned |
URI | https://dx.doi.org/10.1016/j.vaccine.2022.04.094 https://www.ncbi.nlm.nih.gov/pubmed/35550847 https://www.proquest.com/docview/2667428521 https://search.proquest.com/docview/2664788439 |
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