| Literature DB >> 33533663 |
Paul Lingor1, Jan C Koch2, Jeffrey M Statland3, Sumaira Hussain4, Christiane Hennecke5, Joanne Wuu4, Thomas Langbein6, Raees Ahmed5, René Günther7, Benjamin Ilse8, Jan Kassubek9, Katja Kollewe10, Josua Kuttler2, Andreas Leha11, Teresa Lengenfeld2, Thomas Meyer12, Christoph Neuwirth13, Ralf Tostmann5, Michael Benatar4.
Abstract
An inherent challenge to clinical trials that aim to test the efficacy of experimental therapeutics for patients with amyotrophic lateral sclerosis (ALS) is the relative rarity of the disease. A promising solution to this problem is a multi-center approach that ideally includes sites distributed across a broad geographic area. In support of such an approach, the European E-RARE program and the United States National Institutes of Health (NIH) partnered to support the investigator-initiated ROCK-ALS trial (Eudra-CT-Nr.: 2017-003676-31, NCT03792490) as a multi-national collaboration between centers in Europe and North America that is led by European investigators. During the set-up of this international trial, however, a number of unanticipated legal, administrative, and financial complexities emerged that required significant adaptation of the proposed trial scheme. Here, we report our experience navigating these obstacles and describe the potential solutions that we explored. Our experience may inform future efforts to implement multi-national investigator-initiated trials that involve both European and United States centers.Entities:
Keywords: Clinical trial; international; rare disease; regulatory; sister trials
Mesh:
Year: 2021 PMID: 33533663 PMCID: PMC8289747 DOI: 10.1080/21678421.2021.1879866
Source DB: PubMed Journal: Amyotroph Lateral Scler Frontotemporal Degener ISSN: 2167-8421 Impact factor: 3.528