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Study ID Status Title Patient Level Data
RES100769 Terminated A study to assess disease pathology and key therapeutic targets in severe asthma
RES104031 Completed A Randomised (with Respect to Microplaque Treatment Positions), Single-Blind, Placebo-Controlled, Positive-Controlled, Microplaque Study to Assess the Effectiveness of a Topical Formulation of GW786034 in Patients with Chronic Plaque Psoriasis
RES10983 Completed Double blind, randomised, placebo controlled, three periods, crossover study to investigate in a 72 hours enforced smoking cessation severity of withdrawal symptoms and craving in healthy volunteers on Zyban.
RES10988 Completed A randomised, double-blind, triple-dummy, placebo-controlled, five-way cross-over study to investigate the bronchodilatory effects of single doses of salmeterol (25, 50 and 200 mg) and salbutamol (200 mg) over a 24-h period in healthy subjects. Study Listed on ClinicalStudyDataRequest.com
RES11070 Completed A randomised, double-blind, triple-dummy, placebo-controlled, five-way crossover study to investigate the bronchoprotective effects against methacholine challenge and the bronchodilatory effects of single doses of salmeterol (25, 50 and 200 µg) and salbutamol (200 µg) over a 24-hour period in atopic non-asthmatic subjects. Study Listed on ClinicalStudyDataRequest.com
RES11078 500K Affymetric Whole genome scan Completed Multi-Site Collaborative Study for Genotype-Phenotype Associations in Alzheimers disease - GenADA
RES11098 Completed A Randomized, Single-Blind, Placebo-Controlled, Parallel Group, Exploratory Research Study to Describe the Pharmacodynamic Effects of Glyburide, Metformin, and Rosiglitazone versus Placebo for 8 Weeks in Adult Subjects with Type 2 Diabetes Mellitus Study Listed on ClinicalStudyDataRequest.com
RES20044 Completed A double-blind, randomised, single dose, placebo-controlled, crossover design to investigate the efficacy of a new chemical entity (NCE) administered intravenously and subcutaneous sumatriptan in acute migraine.
RES41059 Completed The dose dependent effects of fluticasone propionate on airway responsiveness to adenosine-5-monophopshate (AMP) in mild asthmatic patients.
RES41092 Completed A comparative study of the bronchoprotective effect of single dose inhaled glucocorticosteroid against adenosine 5'-monophosphate (AMP) challenge in mild asthma.
RES41102 Completed A time-course study of the bronchoprotective effect of single dose inhaled fluticasone propionate 250 mg against adenosine 5’-monophosphate (AMP) challenge in mild asthma.
RH01299 Completed The Effect of Fluoride in an Experimental Dentifrice on Remineralization of Erosive Lesions In-Situ
RH01324 Completed A clinical study investigating the efficacy of a dentifrice in providing short term relief from dentinal hypersensitivity
RH01325 Completed A clinical study investigating the efficacy of a dentifrice in providing long term relief from dentinal hypersensitivity
RH01333 Completed A Randomized, Cross-Over, Single Dose Pharmacokinetic Study of 4mg Nicotine Lozenges.
RH01361 Completed Effects of two doses of a common cold treatment on cognitive function
RH01379 Completed A Single Centre, Examiner-blind Human Patch Test of Bactroban Disinfectant Liquid on Normal Skin
RH01381 Completed In Situ Study to Confirm the Anti-caries Potential of a 1.1365% w/w Sodium Monofluorophosphate (1500ppm F) Dentifrice
RH01390 Completed A Clinical Study to Evaluate Experimental Children's Toothpastes in an In-Situ Caries Model
RH01418 Completed A Pharmacokinetic Evaluation of Two Nicotine Patches in Smokers
RH01426 Completed A Proof of Concept Study to Evaluate the Efficacy of an Occlusion Based Dentifrice in the Relief of Dentinal Hypersensitivity
RH01561 Completed Clinical study to evaluate the efficacy of chlorhexidine mouthwashes
RH01589 Completed A Study to Evaluate Relief of Provoked Acute Craving by Nicotine Mouth Film and Nicotine Lozenge
RH01591 Completed A Proof of Concept Study to Evaluate the Efficacy of an Occlusion Based Dentifrice in the Relief of Dentinal Hypersensitivity
RH01619 Completed A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Study to Assess the Efficacy of Once-Daily Fluticasone Propionate Aqueous Nasal Spray 200mcg for 14 Days on Ocular Symptoms Associated with Seasonal Allergic Rhinitis

 

 

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GSK-sponsored clinical studies 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.
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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