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Study ID Status Title Patient Level Data
S3BA1006 Completed A Double-Blind, Randomized, Placebo-Controlled, 2-Way Crossover Study to Determine the Effect of Alosetron 1mg BID on Cholecystokinin-Induced Colonic Motility and Abdominal Pain in IBS Patients
S3BA2001 Completed A 12-week, Dose-ranging, Double-blind, Placebo-controlled Study of Alosetron (GR68755) in Subjects with Irritable Bowel Syndrome
S3BA2002 Completed Characterization of Changes in Regional Brain Activity Associated With Sigmoid Sensitization in IBS Patients Using Positron Emission Tomography (PET) With and Without Alosetron Therapy
S3BA3001 Completed A 12-Week, Randomized, Double-Blind, Placebo-Controlled Study of Alosetron (GR68755) in Female Subjects With Irritable Bowel Syndrome
S3BA3002 Completed A 12-Week, Randomized, Double-Blind, Placebo-Controlled Study of Alosetron (GR68755) in Female Subjects With Irritable Bowel Syndrome
S3BA3003 Completed A 12-Month Randomized, Double-blind, Placebo-controlled Study to Evaluate the Quality of Life and Safety Associated with the Long-term Use of Alosetron (GR68755) in Subjects with Irritable Bowel Syndrome (Final Analysis)
S3BB1002 Completed A Study to Investigate the Effect of Alosetron (4mg), BID for 7½ Days, on 24-Hour Small Bowel Motility, in Patients With Irritable Bowel Syndrome (IBS)
S3BB1004 Completed A study to determine the effects of food on the pharmacokinetics of oral alosetron in healthy volunteers.
S3BB1010 Completed Report of a study to compare the pharmacokinetics of, and tolerability to, a single, oral, 1 mg dose of alosetron in healthy subjects and subjects with renal impairment not requiring dialysis.
S3BB1011 Completed The pharmacokinetics of alosetron 1 mg bid oral administration for 29 days in healthy subjects.
S3BB2009 Completed A Double-Blind Placebo-Controlled Study to Determine the Efficacy of GR68755C (Alosetron) in Treatment of Irritable Bowel Syndrome
S3BB2011 Completed A study to investigate the effects of alosetron on gastrointestinal transit time and rectal sensation in patients with irritable bowel syndrome (IBS).
S3BB3001 Completed A Multicentre, Randomised, Double-blind Comparison of Alosetron 1mg bd against Mebeverine 135mg tds for 12 Weeks in the Treatment of Female Patients with Irritable Bowel Syndrome
S3BB3002 Completed A Multicentre, Randomised, Double-Blind Comparison of Alosetron 1mg bd against Trimebutine 200mg tds for 12 weeks in the Treatment of Female Patients with Irritable Bowel Syndrome.
S3GK01 Completed A Study to Determine the Pharmacokinetics of Orally Administered Ondansetron 16mg in Patients Having Surgery Under General Anaesthesia
S6491365 Completed A Single Dose Bioequivalence Study of 2 different doses of Mini Cherry Nicotine Lozenges
S7120994 Completed Evaluation of the nicotine lozenge in relief of provoked acute craving
S7121359 Completed Evaluation of the Nicotine Mini Lozenge in Relief of Provoked Acute Craving
SALMD/AH90/J85 Completed A phase IV, multi-centre, double-blind, double-dummy, parallel group study to determine whether adult asthmatic patients, currently symptomatic on 400mcg daily inhaled corticosteroid therapy, are better maintained by an increase in corticosteroid dose to 1000mcg daily beclomethasone dipropionate ...
SALMP/AH91/D89 Completed A phase III, multi-centre, double-blind, placebo controlled, parallel group study assessing the efficacy and safety of inhaled salmeterol xinafoate (Serevent™) 50 micrograms BD via the Diskhaler™ when added to the existing treatment of moderate to severe asthmatic children.
SALMP/AH93/J119 Completed A phase IV, multi-centre, double-blind, randomised, parallel group study in general practice to compare the efficacy and tolerability of inhaled salmeterol xinafoate 50 micrograms bd with placebo, both administered via the Diskhaler, in the treatment of episodic asthma induced by upper respirato ...
SAM 106538 Completed Reaching Asthma control with Salmeterol/Fluticasone 50/250 µg bd combination in steroid naive or low dose inhaled corticoid steroid patients by using asthma control test (ACT) comparison of patient self rating with diary card data.
SAM101667 Completed See Detailed Description
SAM103848 Completed See Detailed Description
SAM104926 Completed A multicentre, randomised, double-blind, double dummy, parallel group study to compare the salmeterol/fluticasone propionate combination (SeretideTM) at a dose of 50/100µg twice daily and fluticasone propionate (FlixotideTM) at a dose of 200µg twice daily, both delivered via a dry powder inhaler (DiskusTM) for 12 weeks in asthma in children aged 4-11 years not controlled by inhaled corticosteroids alone at medium dose

 

 

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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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