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Study ID Status Title Patient Level Data
COR100216 Completed A Randomized, Double-Blind, Multi-Center Study Comparing the Effects of Carvedilol Modified Release Formulation (COREG MR) and Atenolol in Combination with and Compared to an Angiotensin Converting Enzyme Inhibitor (Lisinopril) on Left Ventricular Mass Regression in Hypertensive Patients with Left Ventricular Hypertrophy (LVH). Study Listed on ClinicalStudyDataRequest.com
COR103560 Terminated A Randomized, Double-blind, Positive-Controlled, Multicenter Study Comparing the Efficacy of Carvedilol Phosphate Modified Release Formulation (COREG™ MR) and Metoprolol Succinate Extended Release (Toprol-XL®) on the Reduction of Microalbuminuria in Patients with Hypertension and Microalbuminuria. Study Listed on ClinicalStudyDataRequest.com
COR103561 Completed A Randomized, Double-Blind, Multi-Center Study Comparing the Effects of Carvedilol Phosphate Modified Release Formulation (COREG- MR) with Metoprolol Succinate (TOPROL XL) on the Lipid Profile in Normolipidemic, or Mildly Dyslipidemic Hypertensive Patients Study Listed on ClinicalStudyDataRequest.com
COR111096 Completed COR111096, A Randomized, Double-Blind, Active-Controlled, Parallel Group, Multicenter Study Comparing the Proportion of Subjects with Stage 1 or 2 Essential Hypertension Who Achieve Target Blood Pressure While Receiving Either carvedilol CR + lisinopril or lisinopril Monotherapy Study Listed on ClinicalStudyDataRequest.com
CP-97-011 Completed Phase II study of Iodine-131 anti-B1 antibody for 1st or 2nd relapsed indolent B-cell lymphomas or B-cell lymphomas that have transformed to a more aggressive histology.Note: Extensive searching has revealed that no clinical study report is available for this study.
CP-97-012 Completed Phase II study of iodine I 131 Tositumomab for non-Hodgkin’s lymphoma patients who have previously received Rituximab
CP-98-018 Completed A phase I, dose-escalation, open label, multicenter study of Iodine-131 anti-B1 antibody for intermediate- and high-risk B-cell chronic lymphocytic leukemia Study Listed on ClinicalStudyDataRequest.com
CP-98-020 Completed Expanded access study of Iodine-131 anti-B1 antibody for relapsed/refractory low-grade and transformed low-grade non-Hodgkin’s lymphoma
CP-98-021 Completed Retreatment study of patients with non-Hodgkin’s lymphoma who have previously responded to iodine I 131 Tositumomab
CP-98-025 Completed Fludarabine monophosphate followed by Iodine I 131 tositumomab for untreated low-grade and follicular non-Hodgkin’s lymphomaNote: Extensive searching has revealed that no clinical study report is available for this study.
CP-98-028 Completed Phase 1, dose-escalation study of Iodine-131 anti-B1 antibody for patients with previously treated non-Hodgkin’s lymphoma with more than 25% bone marrow involvementNote: Extensive searching has revealed that no clinical study report is available for this study.
CP-99-036 Completed Phase II multicenter study of CVP followed by Iodine-131 anti-B1 antibody for patients with untreated low-grade non-Hodgkin’s lymphoma.Note: Extensive searching has revealed that no clinical study report is available for this study.
CPE107602 Completed A Phase I, Open-Label, Dose-Escalation, First Time in Human Study to Evaluate the Safety Profile, Pharmacokinetics, and Pharmacodynamics of GSK923295 in Subjects with Refractory Cancers
CR2100597 Completed A randomised, double-blind, placebo controlled, 3-way crossover study to evaluate the pharmacodynamics of SB-656933-AAA following single doses in healthy adult subjects undergoing ozone challenge.
CR2100609 Completed A randomised, double-blind, placebo controlled, dose ascending, parallel group study to evaluate the safety, tolerability, steady state pharmacokinetics and pharmacodynamics of SB-656933-AAA following repeated doses in healthy adult subjects. The pharmacokinetic interaction between repeated doses of SB-656933-AAA and single dose of simvastatin will also be assessed
CR2111256 Completed A randomized, double-blind, placebo controlled study to evaluate the safety, tolerability, and pharmacokinetics of SB-656933 following 14 days repeat dosing in healthy male smokers.
CR219039 Completed A dose ranging study to assess the effect of pre-treatment with a single dose of inhaled fluticasone propionate (2 mg, 0.5 mg) on lung inflammation following challenge with inhaled ozone and intermittent exercise in healthy volunteers, relative to placebo. Study Listed on ClinicalStudyDataRequest.com
CR9108914 Terminated A Proof-of-Concept Study Of SB-751689 In Men And Post-menopausal Women With A Fractured Distal Radius Study Listed on ClinicalStudyDataRequest.com
CR9108963 Terminated Study CR9108963: A 12-month, randomized, double-blind, parallel-group, placebo and active-controlled dose-range finding study of the efficacy and safety of SB-751689 in post-menopausal women with osteoporosis Study Listed on ClinicalStudyDataRequest.com
CRH103002 Terminated An open-label, repeat-dose, single-sequence study to investigate the effects of once-daily repeat oral administration of GW876008 125mg on the pharmacokinetics of the combined oral contraceptive in female volunteers
CRH103390 Completed Study CRH103390: A 12 Week Flexible Dose Study of GW876008, Placebo and Active Control (Paroxetine) in the Treatment of Social Anxiety Disorder (SocAD)
CRH108571 Completed Double-blind, randomized, placebo and Alprazolam-controlled three-period crossover incomplete block design study to compare putative anxiolytic-like fRMI activity of GW876008 and GSK561679 after single-dose administration in subjects with Social Anxiety Disorder (SAD)
CRI103143 Completed A Phase IIa, single-centre, randomised, placebo-controlled, double-blind, three-period crossover study investigating the effects on gut autonomic responses of single administrations of either 20 mg or 200 mg GW876008, a CRF1 antagonist, to adult patients with irritable bowel syndrome
CRI105626 Completed A randomised, double-blind, placebo-controlled, crossover study to evaluate efficacy and safety of the CRF1 receptor antagonist GW876008 in patients with Irritable Bowel Syndrome
CRR110744 Completed Phase I, open label drug-drug interaction study in healthy volunteers to evaluate the effect of KALETRA (lopinavir-ritonavir) on GSK706769 pharmacokinetics and to evaluate the pharmacokinetics of a new oral formulation of GSK706769

 

 

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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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