drugset / Trial / NCT02752633

Effect of Allopurinol and Febuxostat on Urinary 2,8-Dihydroxyadenine Excretion

NCT02752633

NaSingle-groupOpen-labelTreatment

Summary

This exploratory pilot study was an open-label, crossover, single-center and non-randomized clinical trial designed to compare the effect of the standardly employed doses of allopurinol (400 mg/day) and febuxostat (80 mg/day) on the urinary 2,8-dihydroxyadenine (DHA) excretion in patients with adenine phosphoribosyltransferase (APRT) deficiency.

Timeline

Start
2013-05
Primary completion
2015-05
Completion
2015-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Allopurinol Small molecule 400 mg
Subject Febuxostat Small molecule 80 mg