drugset / Trial / NCT02288091

A Pilot Study of Inosine in Amyotrophic Lateral Sclerosis (ALS)

NCT02288091

NaSingle-groupOpen-labelTreatment

Summary

This is a single center, open label, 12-week study of inosine treatment. Inosine treatment leads to an increase in the levels of urate (uric acid) in the blood. The primary objective of the study is to determine the tolerability of oral administration of inosine. Secondary study objectives include the measurement of biomarkers of oxidative stress and damage in response to inosine treatment.

Timeline

Start
2015-01
Primary completion
2016-03
Completion
2016-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Inosine Unknown 3 g Oral