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Study ID Status Title Patient Level Data
CAL.201 Completed A multicenter, randomized, double-blind study of the safety and efficacy of emulsion formulation calcipotriene foam 0.005% vs vehicle foam, dovonex; (calcipotriene) ointment 0.005% and vehicle ointment in the treatment of mild to moderate plaque-type psoriasis
CAL.203 Completed A randomized, open-label study to assess the bioavailability of emulsion formulation calcipotriene foam, 0.005%, and dovonex® ointment, 0.005%, in patients with mild to moderate plaque-type psoriasis
CAL10001 Completed An Evaluation of the Bioequivalence of a Combined Formulated Tablet (600mg/300mg abacavir/lamivudine) Compared to ZIAGEN† (abacavir) 2 X 300mg Tablets and EPIVIR† (lamivudine) 2 X 150mg Tablets Administered Concurrently and the Effect of Food on Absorption of the Combined Formulation in Healthy ...
CAL102120 Completed An open-label, two-period, crossover, pharmacokinetic study of abacavir and its intracellular anabolite carbovir triphosphate following once-daily and twice-daily administration of abacavir in HIV-infected subjects.
CAL30001 Completed A phase III, randomized, open-label, parallel, multicenter study to evaluate treatment with fixed-dose combination of abacavir/lamivudine (600mg/300mg) once-daily versus abacavir (300mg) twice-daily and lamivudine (300mg) once-daily in combination with tenofovir once-daily and a new PI or NNRTI for 48 weeks in ART-experienced HIV-1 infected patients
CAR 8902 Completed Report of a study to assess the effects of inhibition and induction of hepatic mixed function oxidase activity on the pharmacokinetics of a single oral dose of carvedilol in 8 healthy volunteers.
CAR-02 Completed A Study of the Pharmacodynamics and Pharmacokinetics of Intravenous Carvedilol in Normal Volunteers.
CAZF4005 Completed Treatment of severe infection with ceftazidime (CAZ) continuous infusion in intensive care patients with continuous veno-venous hemodiafiltration
CBA103679 Completed An open label positron emission tomography (PET) study to investigate brain penetration by [11C]GW842166 in healthy subjects
CBA106191 Completed A double-blind, placebo controlled cross-over study of the effects of the CB2 compound of GW842166 in patients with osteoarthritis
CBA106809 Completed A multi-centre, randomised, single-blind, placebo-controlled, parallel group study to investigate the efficacy of single pre-emptive doses of GW842166X, a non-cannabinoid CB2 receptor agonist, on pain following third molar tooth extraction.
CBA109389 Completed A Multicentre, Randomised, Double-blind, Placebo and Naproxen (500mg) BID controlled, Phase II Proof of Concept, Parallel Group Study to Assess the Efficacy and Safety of Oral GW842166 at Two Dose Levels Administered for 4 weeks in Adults with Osteoarthritis of the Knee
CCR104456 Terminated A Phase III, randomized, double-blind, placebo-controlled, multicenter, parallel group study to compare the efficacy and safety of GW873140 400mg BID in combination with a ritonavir-containing optimized background therapy (OBT) regimen versus placebo plus OBT over 48 weeks.
CCR104458 Terminated A Phase III, randomized, double-blind, placebo-controlled, multicenter, parallel group study to compare the efficacy and safety of GW873140 400mg BID in combination with a ritonavir-containing optimized background therapy (OBT) regimen versus placebo plus OBT over 48 weeks.
CDA 714703/005 Completed A multi-centre, randomised, double-blind, double dummy study comparing the efficacy and safety of chlorproguanil-dapsone-artesunate versus artemether-lumefantrine in the treatment of acute uncomplicated Plasmodium falciparum malaria in children and adolescents in Africa. Study Listed on ClinicalStudyDataRequest.com
CDA 714703/006 Completed A multi-centre, randomised, double-blind study to compare the efficacy and safety of chlorproguanil-dapsone-artesunate versus chlorproguanil-dapsone in the treatment of acute uncomplicated Plasmodium falciparum malaria in children, adolescents and adults in Africa. Study Listed on ClinicalStudyDataRequest.com
CFD105453 Completed A Randomized, Double-Blind, Double-Dummy, Parallel Group, Factorial Design Trial to Assess the Efficacy and Safety of up to Six Weeks Treatment with 20mg, 40mg, or 80mg QD Doses of Carvedilol Controlled Release Formulation (COREG CR) or 10mg, 20mg, or 40mg QD doses of Lisinopril (Zestril) or a Combination of One of the Doses of Each Medication Study Listed on ClinicalStudyDataRequest.com
CFD109701 Completed A study to evaluate the potential incidence of orthostatic hypotension in elderly hypertensive patients following administration of a combination of carvedilol CR and lisinopril Study Listed on ClinicalStudyDataRequest.com
CHN-Nicotine Mint Lozenge-002 Completed A multi-center, randomized, double-blind, parallel, placebo-controlled clinical study to evaluate efficacy and safety of nicotine mint lozenge (2mg and 4mg) in smoking cessation
CIL103657 Completed A Randomized, 24-week, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety and Tolerability of ARIFLO® (15mg BID) in Patients with Chronic Obstructive Pulmonary Disease (COPD) Study Listed on ClinicalStudyDataRequest.com
CNA10905 Completed An Open-Label, Single-Arm, Pharmacokinetic Study of Abacavir and its Intracellular Anabolite Carbovir Triphosphate Following Chronic Administration of an Abacavir 300mg BID Containing Regimen (Ziagen or Trizivir) in HIV Infected Patients
CNA109586 Completed Study of Once-Daily Abacavir/Lamivudine versus Tenofovir/Emtricitabine, Administered with Efavirenz in Antiretroviral-Naive, HIV-1 Infected Adult Subjects
CNA109586_1 Completed Study of Once-Daily Abacavir/Lamivudine versus Tenofovir/Emtricitabine, Administered with Efavirenz in Antiretroviral-Naive, HIV-1 Infected Adult Subjects at 96 weeks
CNA30017 Completed A Phase IIIb, Randomized, Open-Label, Multicenter Study to Evaluate the Safety and Efficacy of 2NRTI/Abacavir versus Continued 2NRTI/PI Treatment in HIV-1 Infected Subjects with Undetectable Plasma HIV-1 RNA Levels
CNA30018 Completed Open-Label Trial to Evaluate the Efficacy, Safety and Tolerance of 1592U89 (Abacavir) in Paediatric Infected Patients With Encephalopathy by HIV: Virological and Immunological Markers in CSF

 

 

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