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Study ID Status Title Patient Level Data
C2380329 Completed An exploratory, observational, cohort study investigating commercially available treatments which may reduce the scab stage of recurrent herpes labialis (RHL)
C6930943 Completed Effects of a common cold treatment on cognitive function
C7100991 Completed To Assess the Subjective Effect of Two Paracetamol Preparations on the Feeling of Breathing in Subjects with the Common Cold.
C7591227 Completed A comparison of solid and soluble forms of cold and influenza remedies
C8843 Completed Multinational/multicentre, non-randomized, open label study to assess efficacy and safety of fondaparinux sodium (ARIXTRA.) use in daily practice in subjects undergoing major orthopedic surgery of the lower limbs
C92_029 Completed A study to evaluate the safety, tolerability and systemic pharmacodynamics effects of salmeterol in the salmeterol/fluticasone propionate (FP)/HFA134a inhaler.
C92-037 Completed To Evaluate the Safety, Tolerability and Pharmacokinetics of Single Doses Fluticasone Propionate/GR106642X Inhaler (500?g, 1000?g and 2000?g) in Healthy Volunteers
C92-050 Completed A study to determine whether the pharmacokinetics, safety or tolerability of subcutaneously administered sumatriptan (6 mg) are altered by interaction with concurrent oral monoamine oxidase inhibitors.
C92-051 Completed A study to investigate the effect of sumatriptan on oesophageal motor function and gastroesophageal reflux.
C92-058 Completed An investigation of the gender differences in the pharmacokinetics of GR68755C.
C92-075 Completed A Study to Assess the Bioavailability of Fluticasone Propionate from a GR106642X Metered Dose Inhaler
C92-079 Completed A study to assess the bioavailability of fluticasone proprionate from a CFC metered dose inhaler containing 1% lecithin
C93-015 Completed A Study to Investigate the Pharmacokinetics of Lamivudine (GR109714X) in Patients with Impaired Hepatic Function
C93-019 Completed A Study to Assess the Absolute Bioavailability of Fluticasone Propionate From a Dry Powder Formulation Using a Multidose Powder Inhaler
C93-020 Completed A study to assess the absolute bioavailability of Fluticasone propionate from dry powder formulation using the Diskhaler®
C93-060 Completed A study to investigate the safety, tolerability, pharmacodynamic and pharmacokinetic response to two doses of oral GR85548A separated by 4 hours.
C93-070 Completed A study to investigate the dose proportionality of oral tablet GR85548A pharmacokinetics in healthy female volunteers.
C93-077 Completed A study to investigate the relative bioavailability of ondansetron syrup and Zofran tablets 4 mg
C93-078 Completed A study to investigate the effect of oral sumatriptan on the intraocular pressure of healthy subjects.
C93-081 Completed A study to investigate the pharmacokinetics of oral GR85548 in subjects with impaired renal function.
C93-085 Completed A study to assess the pharmacokinetics of inhaled fluticasone propionate from a dry powder formulation using the Diskhaler® upon repeat dosing.
C93-087 Completed A study to investigate whether alcohol has an effect on the safety, tolerability, pharmacokinetics or pharmacodynamics of GR85548.
C93-097 Completed A study to determine the dose equivalence for systemic effects for salmeterol compared with salbutamol given by MDI in healthy subjects.
C94-016 Completed A study to investigate the effect of 6mg subcutaneous sumatriptan on oesophageal motility.
C94-027 Completed A Study to Assess the Absolute Bioavailability of Fluticasone Propionate after Oral Doses (0.1 mg, 1 mg, 10 mg)

 

 

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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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