| Literature DB >> 30878059 |
Eliézer N'Goran1, N'da Angbeletchi David Aka1, Mamadou Ouattara1, Eric Huber2, Deon Bezuidenhout3, Elly Kourany-Lefoll4.
Abstract
The importance of implementing paediatric clinical trials for neglected tropical diseases (NTDs) in compliance with the Good Clinical Practices of the International Conference of Harmonisation (ICH-GCP) and other applicable regulatory and ethics guidelines is increasingly being recognised as an essential pathway to provide safe and effective medicines for millions of untreated children living in sub-Saharan Africa (SSA). This paper describes the learnings and challenges faced by the Pediatric Praziquantel Consortium team during the implementation of an industry-sponsored Phase II clinical study in pre-school-aged children infected with schistosomiasis, conducted in remote rural settings in Côte d'Ivoire. The importance of close interactions with the ethics committee, the regulatory and administrative authorities and the rural communities are highlighted. The difficulties faced included obtaining a valid informed consent from the child's parent or guardian, the collection of blood samples from children during the study while respecting cultural beliefs as well as the weak medical research infrastructure. The paper illustrates how a public-private collaborative partnership can promote capacity-building and high-quality NTD paediatric clinical research in SSA.Entities:
Keywords: Bilharzia; Clinical trial; Informed consent; NTDs; Paediatric; Praziquantel; Pre-school-aged children; Schistosomiasis; Sub-saharan Africa; Tropical diseases
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Year: 2018 PMID: 30878059 DOI: 10.1016/bs.apar.2018.09.002
Source DB: PubMed Journal: Adv Parasitol ISSN: 0065-308X Impact factor: 3.870