drugset / Trial / NCT02504320

Phase 1, Febuxostat XR Relative Bioavailability Study

NCT02504320

Phase 1 Completed 78 enrolled Takeda
RandomizedCrossoverOpen-labelBasic science

Summary

This study will assess the relative bioavailability, safety and tolerability following administration of 80 mg single oral doses of 4 febuxostat extended release (XR) formulations.

Timeline

Start
2015-08
Primary completion
2015-09
Completion
2015-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Febuxostat Small molecule 80 mg Oral

Indications

No indication recorded.