drugset / Trial / NCT03836599

A Study to Assess the Safety and Pharmacokinetics of Verinurad and Allopurinol in Asian and Chinese Subjects

NCT03836599

Phase 1 Completed 6 enrolled AstraZeneca Parexel · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a randomized, placebo controlled, double-blind study with two separate cohorts to assess safety, tolerability and pharmacokinetics of verinurad and allopurinol in healthy subjects. In cohort 1, twelve Asian subjects will be treated with allopurinol 300mg for 7 days followed by either allopurinol 300mg and verinurad 24mg or matching placebo for 7 days. In Cohort 2, nine Chinese subjects will be treated with allopurinol 300mg for 7 days followed by allopurinol 300mg and verinurad 12mg administered on 7 out of 8 days.

Timeline

Start
2019-01-16
Primary completion
2019-04-26
Completion
2019-04-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Allopurinol Small molecule 300 mg
Subject Verinurad Small molecule 12 mg
Subject Verinurad Small molecule 24 mg