drugset / Trial / NCT01407874

A Randomized, Double-Blind, Dose-Response Study of the Safety and Uric Acid Effects of Oral Ulodesine Added to Allopurinol in Subjects With Gout and Concomitant Moderate Renal Insufficiency

NCT01407874

Phase 2 Completed 20 enrolled BioCryst Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

To evaluate the overall safety and tolerability of ulodesine when combined with allopurinol in subjects with moderate renal insufficiency.

Timeline

Start
2011-09
Primary completion
2012-07
Completion
2012-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ulodesine Small molecule 5 mg Oral
Subject Ulodesine Small molecule 10 mg Oral