Platform trials - 25/01/23
, Olivier Demarcq b, Silvy Laporte c, Philippe Barthélémy d, Olivier Chassany e, Michel Cucherat f, 1, Jacques Demotes g, 1, Vincent Diebolt h, 1, Hélène Espérou i, 1, Cécile Fouret j, 1, Ariane Galaup k, 1, Laetitia Gambotti l, 1, Charlotte Gourio m, 1, Aurélie Guérin n, 1, Carine Labruyère c, 1, Xavier Paoletti o, 1, Raphael Porcher p, 1, Tabassome Simon q, 1, Nathalie Varoqueaux r, 1Summary |
For the past few years, platform trials have experienced a significant increase, recently amplified by the COVID-19 pandemic. The implementation of a platform trial is particularly useful in certain pathologies, particularly when there is a significant number of drug candidates to be assessed, a rapid evolution of the standard of care or in situations of urgent need for evaluation, during which the pooling of protocols and infrastructure optimizes the number of patients to be enrolled, the costs, and the deadlines for carrying out the investigation. However, the specificity of platform trials raises methodological, ethical, and regulatory issues, which have been the subject of the round table and which are presented in this article. The round table was also an opportunity to discuss the complexity of sponsorship and data management related to the multiplicity of partners, funding, and governance of these trials, and the level of acceptability of their findings by the competent authorities.
Le texte complet de cet article est disponible en PDF.Keywords : Platform trial, Adaptive trial, Randomized controlled trial
Plan
| ☆ | The articles, analyses and proposals resulting from the Giens Workshops are those of the authors and do not prejudge the positions of their organisations. |
Vol 78 - N° 1
P. 29-38 - janvier 2023 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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