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Study ID Status Title Patient Level Data
SX12003 Completed Treatment of depressed and/or anxiety subjects with paroxetine in the primary care.
T3157503 Completed Comparison of the clinical efficacy from the retention phase of fluoride delivery of fluoride toothpastes using an in situ caries model
T3450515 Completed Clinical Efficacy of an Experimental Toothpaste
T3500690 Completed Comparison of enamel remineralization potential of dentifrices incorporating different fluoride salts using an in situ caries model
T3508565 Completed Clinical efficacy of fluoride toothpastes using an in situ caries model
T3508570 Completed Evaluation of plaque fluid fluoride retention from fluoride toothpastes
T3508605 Completed Clinical efficacy of fluoride toothpastes using an in situ caries model
Taiwan-PAR Completed Paroxetine in the Treatment of Chinese Patients with Depressive Episodes – A Double-blind randomized Comparison with Imipramine
TDR3088 Completed Safety, pharmacokinetics and pharmacodynamics (PD) of Org31540/SR90107A after repeated intravenous injection in healthy male volunteers
TDU3085 Completed Safety and pharmacokinetics of ORG31540/SR90107A after a single intravenous injection in healthy male volunteers
TDU3166 Completed A study to investigate the safety, pharmacokinetics and pharmacodynamics (PD) of ORG31540/SR90107A administered as a single intravenous drip to healthy male volunteers
TDU4089 Completed A safety, pharmacokinetics and bioavailability study after single dose subcutaneous administration of Org31540/SR90107A 0.75, 2.5, and 8mg in young adult Japanese healthy male subjects.
TDU4289 Completed A safety and pharmacokinetics study after single dose subcutaneous administration of Org31540/SR90107A 2.5mg in elderly Japanese healthy male volunteers.
THRS/79/0010 (Well 18) Completed Examination of bupropion and diazepam, alone and in combination on human performance tests, subjective rating scales, EEG and autonomic responses.
THRS/81/0012 (Well 07B) Completed Pharmacokinetics in normal volunteers.
THRS/81/0023 (Well 20UK) Completed Effects of low doses of bupropion on plasma prolactin and growth hormone in normal subjects.
THRS/91/0011 (UK19) Completed An Evaluation of the Bioavailability of 250 mg LAMICTAL® Tablets in Normal Volunteers
THRS/91/0023 (UK72) Completed Lamotrigine Pharmacokinetics in Healthy Elderly Volunteers
THRS/91/0025 Completed The Pharmacokinetics of Lamotrigine (BW 430C) in Healthy Subjects with Unconjugated Hyperbilirubinemia (Gilbert’s Syndrome)
THRS/91/0045 Completed Steady-State Pharmacokinetic Study of Lamictal® in Healthy Volunteers Receiving Chronic Doses of Valproic Acid
TMT106386 Completed A Double-Blind, Randomized, Placebo-Controlled, Parallel Group, fMRI and PET Study Comparing Emotional Challenge-induced Regional Cerebral Blood Flow Changes Before and After 8 Weeks of Treatment With Placebo and Paroxetine in Subjects with Social Anxiety Disorder Study Listed on ClinicalStudyDataRequest.com
TOC100224 Completed See Detailed Description Study Listed on ClinicalStudyDataRequest.com
TOC103469 Completed A Randomised, Double-blind, Multicentre, Superiority Placebo-controlled, Phase III Study to Assess the Efficacy and Safety of Topical 1% SB-275833 Ointment versus Placebo Ointment Applied Twice Daily for 5 days in the Treatment of Adults and Paediatric Subjects with Impetigo. Study Listed on ClinicalStudyDataRequest.com
TOC106489 Completed An Open-Label, Non-Comparative Study to Assess the Pharmacokinetics, Safety and Efficacy of Topical Retapamulin (SB-275833) Ointment, 1%, Twice Daily for Five Days in the Treatment of Uncomplicated Skin and Skin Structure Infections in Pediatric Subjects Aged 2 to 24 Months Study Listed on ClinicalStudyDataRequest.com
TOC110977 Completed A Randomized, Double-Blind, Multicenter, Placebo-controlled, Phase III Superiority Study to Assess the Safety and Efficacy of Topical Retapamulin Ointment, 1%, versus Placebo Ointment Applied Twice Daily for 5 Days in the Treatment of Adult and Pediatric Subjects with SITL Study Listed on ClinicalStudyDataRequest.com

 

 

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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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