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Study ID Status Title Patient Level Data
101468/168 Completed A Randomised, Double Blind, Three Period, Cross-Over Study of Ropinirole CR and Ropinirole IR Monotherapy Study Listed on ClinicalStudyDataRequest.com
101468/169 Completed A Phase III, Randomised, Double-blind, Placebo-controlled, Parallel Group Study of Six Months Treatment with Ropinirole CR as Adjunctive Therapy in Patients with Parkinson's Disease who are not Optimally Controlled on L-dopa Study Listed on ClinicalStudyDataRequest.com
101468/170 Completed A follow-up study to observe the long term outcome of Parkinson’s disease in patients who completed Study SK&F 101468/056 or Study SK&F 101468/125.
101468/172 Completed A randomized, 16-week open label, multicenter study of ropinirole to compare tolerability, initial treatment efficacy and patient quality of life of two doses titration schedules
101468/173 Completed Open study to evaluate the safety and efficacy of ropinirole (Requip) in the treatment of new Parkinson Patients or Parkinson patients switching from another dopamine agonist.
101468/180 Completed A clinical evaluation of ropinirole hydrochloride (SK&F101468) used jointly with L dopa for Parkinson's Disease - a double-blind group comparative trial with placebo as comparison
101468/182 Completed Clinical Evaluation of Ropinirole HCl (SK&F101468) as Monotherapy in Parkinson’s Disease – Phase III Open-label Uncontrolled Study –
101468/188 Completed A Study of the Maintained Efficacy and Safety of Ropinirole Versus Placebo in the Long Term Treatment of Restless Legs Syndrome (RLS) Study Listed on ClinicalStudyDataRequest.com
101468/190 Completed A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS). Study Listed on ClinicalStudyDataRequest.com
101468/191 Completed A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Ropinirole in Subjects with Restless Legs Syndrome (RLS) Suffering from Periodic Leg Movements of Sleep (PLMS) Study Listed on ClinicalStudyDataRequest.com
101468/192 Completed A 52 Week Open-Label Extension Study of the Long-Term Safety of Ropinirole in Subjects Suffering from Restless Legs Syndrome (RLS) Study Listed on ClinicalStudyDataRequest.com
101468/194 Completed A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS). Study Listed on ClinicalStudyDataRequest.com
101468/196 Completed 101468/196: A Long-Term, Open-Label Continuation Study of Once Daily Administration of Ropinirole CR Tablets to Patients with Parkinson's Disease who Completed the Previous Ropinirole CR Studies 167 or 164 Study Listed on ClinicalStudyDataRequest.com
101468/197 Completed An open study to compare the PK and tolerability of ropinirole administered as 5 different new formulations with the standard, marketed formulation in healthy volunteers Study Listed on ClinicalStudyDataRequest.com
101468/198 Completed An open, randomised, crossover, healthy volunteer study to compare the PK and tolerability of ropinirole as 3 different new formulations with the standard marketed formulation and to study the effects of a high fat meal on a new formulation Study Listed on ClinicalStudyDataRequest.com
101468/199 Completed An open label study conducted in healthy volunteers to characterize the pharmacokinetics of a new unmarketed formulation of ropinirole Study Listed on ClinicalStudyDataRequest.com
101468/201 Completed A Single Blind, Parallel Group, Up-titration, Phase 1 Study in Healthy Volunteers to Determine a Starting Dose and Select an Up-titration Regimen for a new Formulation of Ropinirole Study Listed on ClinicalStudyDataRequest.com
101468/204 Completed A 12-Week, Randomized, Double-Blind, Parallel Group, Multicentre Study to Assess the Tolerability and Clinical Benefits of Ropinirole Extended Release (XR) Tablets Compared with Ropinirole Immediate Release (IR) Tablets in Subjects with Restless Legs Syndrome (RLS) Study Listed on ClinicalStudyDataRequest.com
101468/205 Completed A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome Study Listed on ClinicalStudyDataRequest.com
101468/206 Completed A 52-Week, Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release (XR) in Patients with Restless Legs Syndrome (RLS) Study Listed on ClinicalStudyDataRequest.com
101468/207 Completed A double-blind, randomized, placebo-controlled, parallel-group study to investigate the tolerability of a dose-escalating regimen of ropinirole in patients suffering from Restless Legs Syndrome (RLS). Study Listed on ClinicalStudyDataRequest.com
101468/218 Completed A Single-Blind, Randomised, Placebo-Controlled, Parallel-Group, Multicentre, Phase IIa Study to Determine the Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Study Listed on ClinicalStudyDataRequest.com
101468/219 Completed An open label, randomised, five-way crossover single-dose pharmacokinetic study to assess dosage strength equivalence of ropinirole CR in healthy male and female volunteers Study Listed on ClinicalStudyDataRequest.com
101468/228 Completed A two year Phase IIIb randomised, multicenter, double-blind, SINEMET controlled, parallel group, flexible dose study, to assess the effectiveness of controlled release ropinirole add-on therapy to L-dopa at increasing the time to onset of dyskinesia in Parkinson's disease subjects. Study Listed on ClinicalStudyDataRequest.com
101468/243 Completed A 52 Week Open-Label Extension Study of the Long-Term Safety of Ropinirole in Subjects Suffering from Restless Legs Syndrome (RLS) Study Listed on ClinicalStudyDataRequest.com

 

 

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