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Study ID Status Title Patient Level Data
C94-034 Completed A study to determine the absolute bioavailability of oral GR85548A.
C94-036 Completed An ascending dose, parallel group study to compare the effects of oral GR85548A on blood pressure in healthy subjects and in hypertensive patients taking anti-hypertensive therapy.
C94-042 Completed A Study to Assess the Absolute Bioavailability of a Single Dose of Inhaled Fluticasone Propionate Administered Via Nebulisation
C94-045 Completed A study to investigate the potential central function effect of GR85548.
C94-057 Completed A study to investigate the effects of the monoamine oxidase A inhibitor, moclobemide, on the pharmacokinetics, safety and tolerability of oral sumatriptan.
C94-071 Completed A study to investigate the safety, tolerability and pharmacokinetics of repeat dosing with oral GR85548A for 5 days.
C95-036 Completed A study to investigate the pharmacokinetics of oral naratriptan (GR85548A) in subjects with impaired hepatic function.
CAE10004 Completed A study to determine the bioequivalence of reformulated 125mg/5mL cefuroxime axetil oral suspension (CAOS) to standard marketed 125mg/5mL suspension at a dose of 250mg. Study Listed on ClinicalStudyDataRequest.com
CAE10005 Completed A study to determine the bioequivalence of reformulated 250mg/5mL cefuroxime axetil oral suspension (CAOS) to standard marketed 250mg/5mL suspension. Study Listed on ClinicalStudyDataRequest.com
CAE40408 Completed An open-label study of sequential therapy with intravenous cefuroxime followed by oral cefuroxime axetil for the treatment of community acquired pneumonia (CAP)
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

 

 

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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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