All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results. Some have, some have not.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Not reported | 2007-005854-21 | A multicenter Phase 2a, randomized, double-blind, placebo-controlled, proof-of-concenpt trial to determine the antiviral activity, pharmacokinetics, tolerability and safety of RDEA806 in HIV-1 positiv... | 2008-06-23 | due-trials |
Ongoing | 2008-002315-41 | Estudio de dosis variables, controlado con placebo, multicéntrico, doble ciego y aleatorio para evaluar la eficacia y seguridad del RDEA806 en pacientes hiperuricémicos con gota sintomática Randomize... | not-yet-due | |
Not reported Terminated | 2008-005113-21 | A Multicenter, Randomized, Double-Blind, Phase 2b Trial to Determine The Efficacy, Tolerability And Safety Of 3 Dose Regimens Of RDEA806 and Open-Label Efavirenz as Active Control in HIV 1-Infected, A... | 2009-08-07 | due-trials |
Reported results | 2009-013055-30 | Randomized, Double-Blind, Multicenter, Placebo-Controlled, Safety and Efficacy Study of RDEA594 Versus Placebo in the Treatment of Hyperuricemia in Patients with Gout | 2012-08-10 | due-trials |
Reported results | 2009-014660-19 | Estudio Multicéntrico, Aleatorizado, Doble Ciego, Controlado con Placebo, de Combinación, para Evaluar la Seguridad, Eficacia y la Posible Interacción Farmacocinética de RDEA594 y Alopurinol en Pacien... | 2016-09-02 | due-trials |
Completed, but no date, and reported results | 2009-014762-26 | A Phase 2, Multiple-Dose, Pharmacokinetic and Pharmacodynamic Study of RDEA594 in Gout Patients with Hyperuricemia and Gout with Renal Insufficiency | bad-data | |
Reported results | 2011-002453-65 | Long-term Allopurinol Safety Study Evaluating Outcomes in Gout Patients (LASSO) | 2013-01-07 | due-trials |
Reported results | 2011-003756-39 | A Phase 3 Randomized, Double-Blind, Multicenter, Placebo- Controlled Study to Assess the Efficacy and Safety of Lesinurad Monotherapy Compared to Placebo in Subjects with Gout and an Intolerance or Co... | 2013-10-23 | due-trials |
Reported results | 2011-003767-29 | A Phase 3 Randomized, Double-Blind, Multicenter, Placebo- Controlled, Combination Study to Evaluate the Efficacy and Safety of Lesinurad and Allopurinol Compared to Allopurinol Alone in Subjects with ... | 2014-05-14 | due-trials |
Reported results | 2011-003768-55 | A Phase 3 Randomized, Double-Blind, Multicenter, Placebo- Controlled, Combination Study to Evaluate the Efficacy and Safety of Lesinurad and Febuxostat Compared to Febuxostat Alone at Lowering Serum U... | 2014-04-17 | due-trials |
Reported results | 2012-002956-18 | A Long-Term Open-Label Extension Study for Subjects Completing a Phase 3 Efficacy and Safety Study of Lesinurad Monotherapy in Subjects with Gout | 2014-06-20 | due-trials |
Reported results | 2012-004389-16 | A Long-Term Extension Study of Lesinurad in Combination with Allopurinol for Subjects Completing an Efficacy and Safety Study of Lesinurad and Allopurinol | 2016-11-17 | due-trials |