| Literature DB >> 32643415 |
Ruben P A van Eijk1,2, Tessa Kliest1, Christopher J McDermott3, Kit C B Roes4, Philip Van Damme5,6, Adriano Chio7,8, Markus Weber9, Caroline Ingre10,11, Philippe Corcia12, Mònica Povedano13, Evy Reviers14, Michael A van Es1, Ammar Al-Chalabi15,16, Orla Hardiman17,18, Leonard H van den Berg1.
Abstract
A change in our current approach toward drug development is required to improve the likelihood of finding effective treatment for patients with amyotrophic lateral sclerosis (ALS). The aim of the Treatment Research Initiative to Cure ALS (TRICALS) is to extend the collective effort with industry and consolidate drug development paths. TRICALS has begun a series of meetings on how to best move the field forward collaboratively, thereby addressing five major topics in ALS clinical trials: (1) preclinical research, (2) biomarker development, (3) eligibility criteria, (4) efficacy endpoints and (5) innovative trial design. There is an appetite for ongoing discussions of these major topics in clinical trials between representatives from academia, patient advocacy groups, industry partners and funding bodies. Industry is open to fundamentally change drug development for ALS and shorten the time to effective therapy for patients by implementing promising innovations in biomarker development, trial design, and patient selection. There is however, a pressing need from all stakeholders for regulatory discussions and amendments of current guidelines to successfully adopt innovation in future clinical development lines.Entities:
Keywords: Clinical trial design; biomarkers; guidelines; preclinical
Year: 2020 PMID: 32643415 DOI: 10.1080/21678421.2020.1788092
Source DB: PubMed Journal: Amyotroph Lateral Scler Frontotemporal Degener ISSN: 2167-8421 Impact factor: 4.092