Journal
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION
Volume 21, Issue 7-8, Pages 496-501Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/21678421.2020.1788092
Keywords
Clinical trial design; biomarkers; preclinical; guidelines
Categories
Funding
- Dutch ALS foundation
- UK Motor Neurone Disease Association (MNDA)
- ALS Liga Belgium
- EU Joint Program Neurodegenerative Disease Research, JPND
- NIHR Sheffield Biomedical Research Center (BRC)
- MRC [MR/R024804/1] Funding Source: UKRI
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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.
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