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Study ID Status Title Patient Level Data
SAS40028 Completed An Open-Label, 12-Week Study to Evaluate the Effects of a Corticosteroid-Sparing Dose of Salmeterol/Fluticasone Propionate Combination Product 50/100mcg twice daily Via the DISKUS Inhaler on Airway Inflammation, Airway Remodeling, and Bronchial Hyperresponsiveness in Adults with Persistent Asthma Study Listed on ClinicalStudyDataRequest.com
SAS40030 Completed A study to investigate switching from usual therapy to the salmeterol/ fluticasone (50/500 mcg) combination Diskus, followed by a reduction of inhaled steroid dosage in patients with moderate to severe asthma
SAS40032 Completed A randomised, parallel-group study of Viani (Salmeterol 50 mcg plus Fluticasone 250 mcg b.i.d.) inhaled from the Diskus® inhaler compared to Budesonide (800-1600 mcg) inhaled from Turbuhaler® plus a long-acting inhaled beta-2-agonist, in subjects with asthma
SAS40036 Completed A multicenter, randomized, double-blind, double-dummy, parallel group, 16-week comparison of asthma control in adolescent and adults receiving either fluticasone propionate/salmeterol Diskus combination product 100/50mcg twice daily, fluticasone propionate Diskus 100mcg twice daily, salmeterol xinafoate 50mcg twice daily, or oral montelukast 10mg every day Study Listed on ClinicalStudyDataRequest.com
SAS40037 Completed A multicenter, randomized, double-blind, double-dummy, parallel group, 16-week comparison of asthma control in adolescents and adults receiving either fluticasone propionate/salmeterol Diskus combination product 100/50mcg twice daily, fluticasone propionate Diskus 100mcg twice daily, salmeterol xinafoate 50mcg twice daily, or oral montelukast 10mg every day Study Listed on ClinicalStudyDataRequest.com
SAS40039 Completed Fluticasone propionate 250 µg plus salmeterol 50 µg (Seretide 50/250 µg bd) combined in a single inhaler (Diskus) in symptomatic patients with mild to moderate asthma previously not treated by maintenance therapy with inhaled corticosteroids and/or long acting beta agonists in adults and childre ...
SAS40066 Completed A Randomized, Open Label, Pilot Crossover Trial, Assessing Patient Preference for Efficacy of Advair Diskus 100/50 (Fluticasone Propionate 100mcg and Salmeterol 50mcg Combination Product 100/50mcg twice daily) and Singulair (Montelukast 10mg every day) in Subjects>15 years of Age with Persistent Asthma Study Listed on ClinicalStudyDataRequest.com
SAS40067 Completed Gaining asthma control with Seretide 50/500 in patients with moderate to severe persistent asthma in general practice.
SAS40068 Completed A 24 week, multicentre, randomized, double-blind, parallel group trial to compare the efficacy and tolerability of salmeterol/fluticasone propionate (ADVAIR) DISKUS inhalation ...
SB020001 Completed A Four-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-group, Multi-Center Study of VENTOLIN™ (albuterol) HFA MDI delivered with facemask and two different holding chambers in Subjects aged 24 to <48 months with asthma symptoms (i.e. wheeze, cough, dyspnea or chest tightness) or consistent with asthma or obstructive airway disease or bronchospasm. Study Listed on ClinicalStudyDataRequest.com
SB030001 Completed A Four-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-group, Multi-Center Study of VENTOLIN™ HFA MDI delivered TID with facemask and valved holding chamber Aerochamber Plus in subjects birth to <24 months in age with symptoms of bronchospasm (i.e. wheeze, cough, dyspnea or chest tightness) consistent with obstructive airways disease. Study Listed on ClinicalStudyDataRequest.com
SB030002 Completed A Randomized, Double-Blind, Parallel-group, Multi-Center Study of Albuterol Sulfate HFA Inhalation Aerosol Delivered Cumulatively with a valved holding chamber and an attached facemask in subjects between birth to 23 months of age with acute wheezing due to obstructive airways disease Study Listed on ClinicalStudyDataRequest.com
SB030003 Completed An Open-Label, Multi-Center Study to Evaluate the Performance and Patient Satisfaction of Albuterol HFA with Counter in Asthma or COPD Subjects at Least 4 Years of Age. Study Listed on ClinicalStudyDataRequest.com
SB29060.833 Completed An open label study assessing Paxil CR (paroxetine CR) in patients with major depressive disorder who discontinued treatment with selective serotonin reuptake inhibitors or a selective serotonin/norepinephrine reuptake inhibitor due to intolerability
SB-462795/008 Completed An open-label, two-period, fixed sequence, randomized, parallel group, interaction study to determine the effects of repeat doses of relacatib on the metabolism of acetaminophen, ibuprofen and atorvastatin in healthy postmenopausal female subjects
SB-480848/026 Completed An international, multicenter, randomized, placebo controlled, parallel-group, 1 year treatment, integrated biomarkers and imaging study in subjects with angiographically documented coronary artery disease (CHD) to examine the effects of the novel lipoprotein-associated phospholipase A2 (Lp-PLA2) in Study Listed on ClinicalStudyDataRequest.com
SB681323/011 Completed An open label study to determine the excretion balance and pharmacokinetics of [14C]SB-681323, administered as a single dose of an oral solution to healthy adult male subjects.
SB-705498/008 Completed A single blind, placebo controlled, multi-centre study to investigate the pharmacokinetics, safety, tolerability and pharmacodynamics of the TRPV1 antagonist SB-705498 against the pain of acute migraine.
SB-714703/003 Completed An open, randomised, multi-centre dose-ranging phase II study to evaluate LAPDAP in combination with three different doses of artesunate.
SBM20001 Completed A single centre, randomised, double-blind, double-dummy, placebo-controlled, parallel group, pilot study to determine the efficacy and safety of 2mg and 4mg doses of Ventolin ™ (salbutamol) syrup for the treatment of cough associated with acute viral upper respiratory tract infection, during a 3 ...
SBM20002 Completed A single centre, randomised, double-blind, placebo-controlled, crossover, pilot study to determine the efficacy and safety of 400 µg and 200 µg doses of Ventolin ™ salbutamol inhaler versus placebo for the treatment of smoking related cough. Study Listed on ClinicalStudyDataRequest.com
SBM40003 Completed A single centre, randomised, double blind, double dummy, cross-over study to measure the topical and systemic effects of Salbutamol delivered by the Turbuhaler inhaler compared with the Diskus dry powder inhaler at high and low flow rates in adult patients with reversible obstructive airways disease. Study Listed on ClinicalStudyDataRequest.com
SCA100223 Completed A Multicenter, Double-Blind, Placebo-Controlled, Fixed-Dose, 8-Week Evaluation of the Efficacy and Safety of Lamotrigine in the Treatment of Depression in Patients with Type II Bipolar Disorder Study Listed on ClinicalStudyDataRequest.com
SCA102833 Completed The Evaluation of Lamictal as an Add-on Treatment for Bipolar I Disorder in Children and Adolescents, 10 to 17 Years of Age Study Listed on ClinicalStudyDataRequest.com
SCA104753 Completed An Open-Label Extension Study to Assess the Safety of Lamotrigine in Subjects with Bipolar Disorder, who are in remission following a manic/hypomanic index episode or a depressive index episode.

 

 

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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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