Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III
- PMID: 19743457
- PMCID: PMC2854625
- DOI: 10.1002/ana.21743
Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III
Abstract
Objective: Amyotrophic lateral sclerosis (ALS) is a devastating, and currently incurable, neuromuscular disease in which oxidative stress and mitochondrial impairment are contributing to neuronal loss. Coenzyme Q10 (CoQ10), an antioxidant and mitochondrial cofactor, has shown promise in ALS transgenic mice, and in clinical trials for neurodegenerative diseases other than ALS. Our aims were to choose between two high doses of CoQ10 for ALS, and to determine if it merits testing in a Phase III clinical trial.
Methods: We designed and implemented a multicenter trial with an adaptive, two-stage, bias-adjusted, randomized, placebo-controlled, double-blind, Phase II design (n = 185). The primary outcome in both stages was a decline in the ALS Functional Rating Scale-revised (ALSFRSr) score over 9 months. Stage 1 (dose selection, 35 participants per group) compared CoQ10 doses of 1,800 and 2,700 mg/day. Stage 2 (futility test, 75 patients per group) compared the dose selected in Stage 1 against placebo.
Results: Stage 1 selected the 2,700 mg dose. In Stage 2, the pre-specified primary null hypothesis that this dose is superior to placebo was not rejected. It was rejected, however, in an accompanying prespecified sensitivity test, and further supplementary analyses. Prespecified secondary analyses showed no significant differences between CoQ10 at 2,700 mg/day and placebo. There were no safety concerns.
Interpretation: CoQ10 at 2,700 mg daily for 9 months shows insufficient promise to warrant Phase III testing. Given this outcome, the adaptive Phase II design incorporating a dose selection and a futility test avoided the need for a much larger conventional Phase III trial.
Conflict of interest statement
Conflict of Interest Statement: PK, JLPT, GL, RB, BL have no conflict of interest. HM received honoraria for Advisory Board participation from Avanir, Eisai, Knopp, Neuralstem and Otsuka, and also received grants for clinical trials from Avanir and Knopp. EPP received honoraria for Advisory Board participation from Avanir.
Figures




References
-
- Annegers JF, Appel S, Lee JR, Perkins P. Incidence and prevalence of amyotrophic lateral sclerosis in Harris County, Texas, 1985-1988. Arch Neurol. 1991;48:589–593. - PubMed
-
- Traynor BJ, Codd MB, Corr B, et al. Incidence and prevalence of ALS in Ireland, 1995-1997: a population-based study. Neurology. 1999;52:504–509. - PubMed
-
- Sorenson EJ, Stalker AP, Kurland LT, Windebank AJ. Amyotrophic lateral sclerosis in Olmsted County, Minnesota, 1925 to 1998. Neurology. 2002;59:280–282. - PubMed
-
- Norris F, Shepherd R, Denys E, et al. Onset, natural history and outcome in idiopathic adult motor neuron disease. J Neurol Sci. 1993;118:48–55. - PubMed
-
- Traynor BJ, Alexander M, Corr B, et al. An outcome study of riluzole in amyotrophic lateral sclerosis--a population-based study in Ireland, 1996-2000. J Neurol. 2003;250:473–479. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- 1 UL1 RR024156/RR/NCRR NIH HHS/United States
- M01-RR023940/RR/NCRR NIH HHS/United States
- R01 NS48125/NS/NINDS NIH HHS/United States
- UL1 RR024156/RR/NCRR NIH HHS/United States
- UL1 RR024992/RR/NCRR NIH HHS/United States
- R01 NS048555/NS/NINDS NIH HHS/United States
- UL1 TR000448/TR/NCATS NIH HHS/United States
- K12RR017648/RR/NCRR NIH HHS/United States
- R01 NS048125/NS/NINDS NIH HHS/United States
- K12 RR017648/RR/NCRR NIH HHS/United States
- R01 NS48555/NS/NINDS NIH HHS/United States
- M01-RR01066/RR/NCRR NIH HHS/United States
- M01 RR001066/RR/NCRR NIH HHS/United States
- M01 RR023940/RR/NCRR NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous