drugset / Trial / NCT00227266

Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy

NCT00227266 ↗

RandomizedCrossoverQuadruple-blindTreatment

Summary

This is a multi-center trial to assess safety and efficacy of a combined regimen of oral valproic acid (VPA) and carnitine in patients with Spinal Muscular Atrophy (SMA) 2 to 17 years of age. Cohort 1 is a double-blind placebo-controlled randomized intention to treat protocol for SMA "sitters" 2 - 8 years of age. Cohort 2 is an open label protocol for SMA "standers and walkers" 3 - 17 years of age to explore responsiveness of efficacy outcomes. Outcome measures will include blood chemistries, functional testing, pulmonary function testing, electrophysiological evaluations, PedsQL quality of life assessment, quantitative assessments of survival motor neuron (SMN) mRNA from blood samples, growth and vital sign parameters. Six centers will enroll a total of 90 patients.

Timeline

Start
2005-09
Primary completion
2007-11
Completion
2007-11

Outcome

Missed primary endpoint

paper there was no difference in change from the baseline MHFMS score between treatment and placebo groups PMID 20808854 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject L-carnitine Other / unclassified 50 mg/kg Oral
Subject Valproic Acid Small molecule 10 mg/kg Oral
Subject Valproic Acid Small molecule 20 mg/kg Oral