drugset / Trial / NCT02752633
Effect of Allopurinol and Febuxostat on Urinary 2,8-Dihydroxyadenine Excretion
Phase 4
Completed
9 enrolled
Landspitali University Hospital
Mayo Clinic · collabNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Allopurinol | Small molecule | 400 mg | — |
| Subject | Febuxostat | Small molecule | 80 mg | — |