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DOI 10.1093/cid/ciaf094

Медицинская библиотека · Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025

Enhancing Clinical Trial Sites in Low- and Middle-Income Countries to Facilitate Product Development in Response to the COVID-19 Pandemic.

Kang Sophie S Y, Tadesse Birkneh Tilahun, Jeon Hyon Jin, Fallah Mosoka P, Dereje Nebiyu, Ilesanmi Olayinka Stephen, Abay Solomon Mequanente, Tekle Betelhem I, Son Hayoung G, Shrestha Laxman, Shrestha Anita, Ramiso Hasia V, Canouet Vincent, Kim Yeonseon, Asante Kwaku Poku, Anim Japhet, Kaali Seyram, Capeding Maria Rosario, Jani Ilesh V, Capitine Igor, Mahumane Arlete, Wartel T Anh, Haselbeck Andrea Haekyung, Saluja Tarun, Marks Florian

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

The swift development of coronavirus disease 2019 (COVID-19) vaccines marked a monumental effort in global coordination and collaboration; however, there remained major disparities in vaccine access and research capacity across countries. Unequal participation in vaccine development studies from low- and middle- income countries (LMICs) clearly signaled an urgent need to strengthen health research infrastructure in those regions.

METHODS

With funding from the Gates Foundation (GF), this site readiness initiative carried out rapid capacity enhancement activities to enable large-scale, Phase 3 pivotal clinical trial conduct in LMICs. The International Vaccine Institute (IVI) worked with site partners in four countries (Mozambique, Ghana, Nepal, and the Philippines) after conducting feasibility assessments for site selection. Site-specific gaps were identified, and capacity building activities focused on staff training, site infrastructure, and resource mobilization were carried out over roughly 7 months from October 2020 to May 2021.

RESULTS

Despite pandemic-related challenges such as supply chain shortages, by the end of the capacity building efforts all sites were either contracted to or in discussions with trial sponsors to conduct severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine studies. This article provides an overview of the site selection process, critical components of site establishment, and final site readiness evaluations carried out amidst a global health emergency.

CONCLUSIONS

This experience illustrates the value of research capacity enhancement as essential to both pandemic preparedness and global health equity. The lessons learned are being carried into an ongoing initiative across West Africa, currently underway as the "Advancing Research Capabilities in West Africa (ARC-WA)."

Для цитирования: Kang Sophie S Y, Tadesse Birkneh Tilahun, Jeon Hyon Jin, Fallah Mosoka P, Dereje Nebiyu, Ilesanmi Olayinka Stephen, Abay Solomon Mequanente, Tekle Betelhem I, Son Hayoung G, Shrestha Laxman, Shrestha Anita, Ramiso Hasia V, Canouet Vincent, Kim Yeonseon, Asante Kwaku Poku, Anim Japhet, Kaali Seyram, Capeding Maria Rosario, Jani Ilesh V, Capitine Igor, Mahumane Arlete, Wartel T Anh, Haselbeck Andrea Haekyung, Saluja Tarun, Marks Florian. Enhancing Clinical Trial Sites in Low- and Middle-Income Countries to Facilitate Product Development in Response to the COVID-19 Pandemic.. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2025. DOI: 10.1093/cid/ciaf094.

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