Tranilast
DrugTranilast tablets, 300 mg, QD
NCT Number: NCT00995618
This is a randomized, double-blind, 3-period crossover phase 2 study in patients with documented hyperuricemia to evaluate the effect of tranilast on febuxostat pharmacokinetics (PK) and pharmacodynamics (PD) and to evaluate the effect of febuxostat on tranilast PK and PD as measured by reduction in serum uric acid levels.
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Notify Me18 year–70 year
All sexes
Interventional
Phase 2
Nuon Investigative Site, Honolulu, Hawaii, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tranilast tablets, 300 mg, QD
Febuxostat Tablets, 40 mg, QD
Other names: Uloric
Tranilast, 300 mg QD; Febuxostat, 40 mg QD
Time frame: Seven days
Time frame: 7 days
Nuon Therapeutics, Inc.
Industry
A Randomized, Double-Blind, Crossover, Pharmacodynamic and Pharmacokinetic Drug Interaction Study of Tranilast in Combination With Febuxostat Compared With Tranilast Alone and Febuxostat Alone in Healthy Subjects With Hyperuricemia
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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