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A Study to Assess the Safety and Pharmacokinetics of Verinurad and Allopurinol in Asian and Chinese Subjects
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.
Details
| Lead sponsor | AstraZeneca |
|---|---|
| Phase | PHASE1 |
| Status | COMPLETED |
| Enrolment | 6 |
| Start date | Wed Jan 16 2019 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Fri Apr 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Chronic Kidney Disease
Interventions
- Verinurad
- Allopurinol
- Placebo
Countries
United States