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Study ID Status Title Patient Level Data
RRL103628 Completed An Open-Label, Parallel-Group, Repeat-Dose Study to Investigate the Effects of End Stage Renal Disease and Haemodialysis on the Pharmacokinetics of Ropinirole (Study RRL103628) Study Listed on ClinicalStudyDataRequest.com
RRL103660 Completed A 12-Week, Multi-Center, Double-Blind, Placebo-Controlled, Parallel Group, Flexible Dose Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome (RLS) in RLS Patients with Sleep Disturbance and Periodic Limb Movements (PLM) During Sleep Study Listed on ClinicalStudyDataRequest.com
RRL106721 Completed A multicenter 3:1-randomized placebo-controlled double-blind Phase IIIb study on the effects of Ropinirole on mood/(subclinical) depression in the therapy of patients with moderate to severe idiopathic RLS in Germany
RXP110908 Completed Study RXP110908, a polysomnography study of GSK1838262 (XP13512) extended release tablets versus placebo in the treatment of Restless Legs Syndrome (RLS) and associated sleep disturbance
S2090309 Completed An Evaluation of a Low Dose Nicotine Lozenge in Relief of Provoked Acute Craving
S2110367 Completed A Randomized, Open Label Study to Evaluate the Oral Tolerability of a Nicotine Prototype
S2111378 Completed A Pilot Study to Evaluate Relief of Provoked Acute Craving by Nicotine Mouth Strip, Nicorette ® Nicotine Lozenge and Gum
S2540345 Completed An evaluation of the 4mg nicotine mint lozenge for the relief of cognitive impairment associated with nicotine withdrawal
S2B-121 Completed Evaluation of the Anatomic Site of Absorption of Sumatriptan (GR43175).
S2B-124 Completed A Study to Evaluate the Bioequivalence of 50 and 100mg Sumatriptan Tablets.
S2B-199 Completed The evaluation of electrocardiograms following a single 100mg oral dose of GR43175C administered to healthy male volunteers.
S2B-201 Completed Evaluation of the safety and efficacy of subcutaneous GR43175C in migraine patients.
S2B203 Completed Evaluation of the effect of GR43175C on blood pressure in hypertensive migraine patients.
S2B210 Completed Efficacy of subcutaneous sumatriptan administered by the Glaxo autoinjector device- Protocol S2B210
S2B211 Completed Efficacy of subcutaneous sumatriptan administered by the Glaxo autoinjector device- Protocol S2B211.
S2B222 Completed A study to investigate the effects of subcutaneous GR43175C on the coronary vasculature in patients with existing or suspected coronary artery disease.
S2B307 Completed Repeat-dose efficacy and laboratory safety trial of subcutaneous GR43175C in migraine patients.
S2B308 Completed Evaluation of sumatriptan in the treatment of migraine pain recurrence- a pilot study.
S2B308E Completed Evaluation of sumatriptan in the treatment of migraine pain recurrence- extension.
S2B-341 Completed A double-blind, placebo-controlled, parallel group study to evaluate two dose levels (10mg and 20mg) of intranasal sumatriptan in the acute treatment of a migraine attack.
S2B-H27 Completed A study to determine whether ergotamine (0.25mg given intravenously) has any effect on the pharmacodynamics and pharmacokinetics of GR43175C in healthy subjects.
S2BP31 Completed The treatment of chronic tension-type headache with subcutaneous GR43175C – a placebo-controlled dose-comparison study.
S2BP33 Completed A study to investigate the effects on the coronary vasculature of the 5HT1-like receptor agonist, GR43175C, in subjects with existing coronary artery disease.
S2BP42 Completed A single-blind two-part study to rechallenge with subcutaneous GR43175C, patients who had previously experienced an adverse event involving discomfort or pain in the chest following GR43175C administration.
S2BP49 Completed A study to investigate the effects of subcutaneous GR43175C on the coronary vasculature in patients with existing or suspected coronary artery disease.

 

 

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GSK-sponsored clinical trials are those for which GSK is ultimately responsible for all aspects of the study even if some or all of these activities are transferred to another party.

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