A review of patient-reported outcomes used for regulatory approval of oncology medicinal products in the European Union between 2017 and 2020

IntroductionCancer and corresponding available treatments are associated with substantial symptoms and functional limitations. In this context, collection of patient-reported outcomes (PRO) in clinical trials gained special interest and is recommended by regulatory authorities. Within clinical trial...

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Bibliographic Details
Main Authors: Maria Manuel Teixeira, Fábio Cardoso Borges, Paula Sousa Ferreira, João Rocha, Bruno Sepodes, Carla Torre
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Medicine
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Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2022.968272/full