Literature DB >> 23217117

Challenges of non-commercial multicentre North-South collaborative clinical trials.

Raffaella M Ravinetto, Ambrose Talisuna, Maaike De Crop, Harry van Loen, Joris Menten, Chantal Van Overmeir, Halidou Tinto, Raquel Gonzalez, Martin Meremikwu, Carolyn Nabasuma, Ghyslain M Ngoma, Corine Karema, Yeka Adoke, Mike Chaponda, Jean-Pierre Van Geertruyden, Umberto D'Alessandro.   

Abstract

The last decade has witnessed a substantial increase of multi-centre, public health-oriented clinical trials in poor countries. However, non-commercial research groups have less staff and financial resources than traditional commercial sponsors, so the trial teams have to be creative to comply with Good Clinical Practices (GCP) requirements. According to the recent experience of a large multicentre trial on antimalarials, major challenges result from the complexity of multiple ethical review, the costs of in-depth monitoring at several sites, setting up an adequate Good Clinical Laboratory Practices (GCLP) framework, lack of insurers in host countries, and lack of adequate non-commercial data management software. Public research funding agencies need to consider these challenges in their funding policies. They also could support common spaces where North-South collaborative research groups may share critical information, such as on research insurance and open-source, GCP-compliant software. WHO should update its GCP guidelines, which date back to 1995, to incorporate the perspectives and needs of non-commercial clinical research.
© 2012 Blackwell Publishing Ltd.

Mesh:

Year:  2012        PMID: 23217117     DOI: 10.1111/tmi.12036

Source DB:  PubMed          Journal:  Trop Med Int Health        ISSN: 1360-2276            Impact factor:   2.622


  6 in total

1.  Sponsorship in non-commercial clinical trials: definitions, challenges and the role of Good Clinical Practices guidelines.

Authors:  Raffaella Ravinetto; Katelijne De Nys; Marleen Boelaert; Ermias Diro; Graeme Meintjes; Yeka Adoke; Harry Tagbor; Minne Casteels
Journal:  BMC Int Health Hum Rights       Date:  2015-12-30

2.  Strengthening neglected tropical disease research through enhancing research-site capacity: an evaluation of a novel web application to facilitate research collaborations.

Authors:  Tamzin Furtado; Samuel Franzen; Francois van Loggerenberg; Gwenaelle Carn; Shannon Grahek; Megan McBride; Maureen Power; Jennifer O'Reilly; Barbara Savarese; Margaret Ann Snowden; Gwynn Stevens; Almarie Uys; Trudie Lang
Journal:  PLoS Negl Trop Dis       Date:  2014-11-13

3.  Clinical Research in Neglected Tropical Diseases: The Challenge of Implementing Good Clinical (Laboratory) Practices.

Authors:  Raffaella Ravinetto; Emilie Alirol; Yodi Mahendradhata; Suman Rijal; Pascal Lutumba; Moussa Sacko; Sayda El-Safi; Kruy Lim; Harry van Loen; Jan Jacobs; Rosanna W Peeling; Francois Chappuis; Marleen Boelaert
Journal:  PLoS Negl Trop Dis       Date:  2016-11-03

4.  "You can save time if…"-A qualitative study on internal factors slowing down clinical trials in Sub-Saharan Africa.

Authors:  Nerina Vischer; Constanze Pfeiffer; Manuela Limacher; Christian Burri
Journal:  PLoS One       Date:  2017-03-16       Impact factor: 3.240

5.  It is time to revise the international Good Clinical Practices guidelines: recommendations from non-commercial North-South collaborative trials.

Authors:  Raffaella Ravinetto; Halidou Tinto; Ermias Diro; Joseph Okebe; Yodi Mahendradhata; Suman Rijal; Eduardo Gotuzzo; Pascal Lutumba; Alain Nahum; Katelijne De Nys; Minne Casteels; Marleen Boelaert
Journal:  BMJ Glob Health       Date:  2016-11-16

6.  Development of the Good Health Research Practice course: ensuring quality across all health research in humans.

Authors:  Patricia Henley; Varalakshmi Elango; Olaf Horstick; Riris Andono Ahmad; Christine Maure; Pascal Launois; Corinne Merle; Jamila Nabieva; Yodi Mahendradhata
Journal:  Health Res Policy Syst       Date:  2017-03-31
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.