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Clinical Trial
. 2018 Feb;57(2):193-199.
doi: 10.1002/mus.25776. Epub 2017 Sep 18.

Clinical trial of L-Carnitine and valproic acid in spinal muscular atrophy type I

Affiliations
Clinical Trial

Clinical trial of L-Carnitine and valproic acid in spinal muscular atrophy type I

Kristin J Krosschell et al. Muscle Nerve. 2018 Feb.

Abstract

Introduction: The aim of this study was to determine the safety and therapeutic potential of L-carnitine and valproic acid (VPA) in infants with spinal muscular atrophy (SMA).

Methods: Our investigation was an open-label phase 2 multicenter trial of L-carnitine and VPA in infants with SMA type I with retrospective comparison to an untreated, matched cohort. Primary outcomes were: safety and adverse events; secondary outcomes were survival, time to death/>16 hours/day of ventilator support; motor outcomes; and maximum ulnar compound motor action potential amplitude.

Results: A total of 245 AEs were observed in 35 of the 37 treated subjects (95%). Respiratory events accounted for 49% of all adverse events, resulting in 14 deaths. Survival was not significantly different between treated and untreated cohorts.

Discussion: This trial provides evidence that, in infants with SMA type I, L-carnitine/VPA is ineffective at altering survival. The substantial proportion of infants reaching end-points within 6 months of enrollment underscores the urgent need for pre-symptomatic treatment in SMA type I. Muscle Nerve 57: 193-199, 2018.

Keywords: L-carnitine; clinical trials; infants; natural history; spinal muscular atrophy type I; valproic acid.

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