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Study ID Status Title Patient Level Data
WHP8880 Completed A study to investigate the absolute bioavailability of subcutaneous and oral GR43175C.
WMH/84/013 Completed The effect of oral GR33343X in five healthy subjects.
WXL108709 Completed A cross-over study to evaluate the effect of WELLBUTRIN XL on intraocular pressure in healthy volunteers
Z3120510 Completed Exploratory evaluation of an experimental fluoride dentifrice formulation using an in situ remineralization/fluoride uptake model
Z3480664 Completed Evaluation of a test mouthwash and dentifrice regimen in an in-situ model of dental erosion
Z36420889 Completed A clinical study to evaluate the effect of a commercial cosmetic mouth rinse on plaque re-growth
Z3690607 Completed An exploratory clinical study to evaluate the efficacy of two currently marketed toothpastes containing different concentrations of a tubule occlusion agent
Z3770631 Completed An exploratory study investigating the effects of a potassium nitrate solution in reducing dentinal hypersensitivity
Z3770633 Completed A proof of principle study investigating the effects of a potassium nitrate solution in reducing dentinal hypersensitivity
Z6961385 Completed A Placebo Controlled Study to Evaluate the Effectiveness of Experimental Foaming Gel Toothpastes Using an In-situ Erosion Remineralization Model
Z7871335 Completed A Pilot Clinical Study Investigating the Efficacy of a Toothpaste in Providing Immediate and Short Term Relief from Dentinal Hypersensitivity
ZDVB1003 Completed A phase I study to evaluate the pharmacokinetics and safety of RETROVIR (zidovudine, ZDV) administered orally in combination with EPIVIR™ (lamivudine, 3TC) to HIV-1 infected pregnant women and their offspring.
ZEFT02 Completed Open-label study of lamivudine in combination with interferon in treating chronic hepatitis B, anti HBe positive patients who are interferon-therapy naïve.
ZEFT03 Completed Open label treatment with lamivudine in patients with chronic hepatitis B, Anti HBe (Hepatitis B envelope) Positive, who have not responded to previous treatment with interferon. Study of lamivudine added to the interferon treatment in comparison to the sequential treatment
ZM2005/00181/01 Completed Avandia Cardiovascular Event Modeling Project
ZOF-011/2002 Completed Open label treatment observational cohort (TOC) of a Single Dose Therapy with Zofran for the Prevention and Therapy of Chemotherapy-induced Nausea and Emesis (CINV)
ZOV30008 Completed A Phase III Multicentre, Double-Blind, Active-Controlled, Parallel Study Comparing the Efficacy and Safety of ZOVIRAX Cold Sore Cream (Aciclovir 5% Cream) and Lidocaine 2% to ZOVIRAX Cold Sore Cream Alone Administered for 5 Days in Subjects with Herpes Labialis Infection.
ZOV30009 Completed A Phase III Multicentre, Double-Blind, Active-Controlled, Parallel Study Comparing the Efficacy and Safety of ZOVIRAX Cold Sore Cream (Aciclovir 5% Cream) and Lidocaine 2% to ZOVIRAX Cold Sore Cream Alone Administered for 5 Days in Subjects with Herpes Labialis Infection.
ZVC111449 Completed Bioequivalence study of Aciclovir 5% cream - Bioequivalence study of Aciclovir cream between Current and New formulation in Japanese Healthy volunteers -
ZVX10001 Completed Skin Safety Study of Aciclovir Cream 5%
ZYB 30011 Completed A multicentre, randomised, double- blind, placebo controlled study to evaluate the efficacy and tolerability of bupropion hydrochloride (SR) sustained release (2 x 150mg per day) versus placebo as an aid to smoking cessation in smokers with at least one cardiovascular (CV) risk factor.
ZYB30005 Completed An open-label, multicentre study with general practitioners to assess efficacy and safety of Bupropion SR (2x150mg) dependent on (sub)-depression and motivation
ZYB30009 Completed A multi-centre, randomised, double-blind, placebo controlled, 6 month study to evaluate the efficacy and tolerability of bupropion hydrochloride sustained release tablets for the treatment of nicotine dependence as an aid to smoking cessation in a healthcare professionals and hospital staff popu ...
ZYB40001 Completed A randomized, double-blind, placebo-controlled, 12-week smoking cessation trial of Zyban (150 mg bid) in adult smokers previously treated with Zyban
ZYB40003 Completed A multicenter, randomized, parallel, placebo-controlled, one-year study of the efficacy and safety of bupropion hydrochloride sustained-release tablets versus placebo as an aid to smoking cessation treatment in adult cigarette smokers previously treated with bupropion 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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