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Study ID Status Title Patient Level Data
FLTA4024 Completed Double-blind, double-dummy, randomized, parallel group comparison of fluticasone proprionate aqueous nasal spray versus encapsulated loratadine tablets versus a combination of fluticasone proprionate and loratadine versus placebo for two weeks in subjects with seasonal allergic rhinitis
FLTA4025 Completed A randomized, double-blind, placebo-controlled study examining the effect of fluticasone propionate aqueous nasal spray 200mcg QD used in conjunction with an antibiotic in allergic and nonallergic subjects with recurrent sinusitis
FLTA4030 Completed A Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, Parallel-Group, Comparative Study of Inhaled Fluticasone Propionate (88mcg BID) Versus Zafirlukast (20mg BID) in Subjects Who Are Currently Receiving Beta-Agonists Alone
FLTA4031 Completed A Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, Parallel-Group, Comparative Study of Inhaled Fluticasone Propionate (88mcg BID) Versus Zafirlukast (20mg BID) in Subjects Who Are Currently Receiving Beta-Agonists Alone
FLTA4033 Completed A randomized, double-blind, placebo-controlled study examining the effect of fluticasone propionate aqueous nasal spray 200?g QD in subjects with an acute episode of recurrent sinusitis
FLTA4034 Completed A Randomized, Double-Blind, Double-Dummy, Parallel-Group, Comparative Study Of Inhaled Fluticasone Propionate 88mcg BID Versus Zafirlukast 20mg BID In Asthmatic Subjects Who Are Currently Receiving Low Dose Inhaled Corticosteroids
FLTA4035 Completed A Randomized, Double-Blind, Double-Dummy, Parallel-Group, Comparative Study Of Inhaled Fluticasone Propionate 88mcg BID Versus Zafirlukast 20mg BID In Asthmatic Subjects Who Are Currently Receiving Low Dose Inhaled Corticosteroids
FLTA4039 Completed A randomized, double-blind, parallel group comparison study of inhaled fluticasone propionate (88mcg BID) versus montelukast sodium (10mg QD) in subjects currently receiving beta agonists alone.
FLTB1001 Completed To compare the effects of the dosing schedule of inhaled Fluticasone propionate using various tests of HPA-axis function.
FLTB1003 Completed A study to assess the effects of ketoconazole on the pharmacokinetics and systemic pharmacodynamics of inhaled fluticasone propionate in healthy volunteers
FLTB1006 Completed Pharmacokinetic and pharmacodynamic evaluation of Fluticasone propionate and Budesonide after single and bi-daily inhaled administration over 5 days
FLTB1009 Completed A study to investigate the plasma concentrations of fluticasone propionate (FP) after intranasal administration of four 800 mg doses of FP given over two days as either preservative-free nasal drops or an aqueous nasal spray.
FLTB1016 Completed A randomised, double blind (with respect to placebo within a device), incomplete block design study to assess the systemic pharmacodynamics and pharmacokinetics of intranasal and intravenous fluticasone propionate administered via either: a nasal aerosol in propellant HFA134a (200µg, 2400µg), an ...
FLTB1020 Completed A Dose Proportionality Study of Fluticasone Propionate from 50, 125, and 250mcg HFA Inhalers and Comparability to 125 and 250mcg CFC Inhalers
FLTB3001 Completed A multicentre, randomised, double blind, parallel group study to compare the oral steroid-sparing effect of nebulised fluticasone propionate 2mg twice daily and 0.5mg twice daily with placebo in patients with chronic severe asthma.
FLTB3002 Completed A multicentre, randomised, double-blind, parallel group clinical trial to determine the safety and efficacy of nebulised fluticasone propionate 1mg twice daily compared with oral soluble prednisolone administered for 7 days to children aged 4 to 16 years with an acute asthma exacerbation.
FLTB3004 Completed A multicentre, randomised, double-blind, parallel-group study to compare the efficacy and tolerability of fluticasone proprionate 100mg bd administered by pressurised inhaler propelled by a mixture of propellants 11 and 12 or by an alternative propellant, GR106642X for a period…
FLTB3006 Completed A multicentre, randomised, double-blind, crossover study to compare the efficacy and tolerability of fluticasone propionate 2 mg daily administered by pressurised inhaler propelled by a mixture of propellants 11/12 or by an alternative propellant, GR106642X in adult patients with severe reversib ...
FLTB3009 Completed A multicentre, randomised, double-blind, double-dummy, parallel-group study to determine the clinical equivalence between fluticasone propionate 250mg twice daily delivered via a multidose powder inhaler (MDPI) and the Diskhaler in adult patients with reversible airways disease.
FLTB3012 Completed A multicentre, randomised, double-blind, parallel group study to compare the efficacy and tolerability of fluticasone propionate (250 mg bd) administered by pressurised inhaler propelled by a mixture of propellants 11 and 12 or by an alternative propellant, GR106642X in adult patients…
FLTB3013 Completed A multi-centre, randomised, double-blind, parallel-group clinical trial to compare the safety and efficacy of the dry powder formulation of fluticasone propionate 400mg/day and beclomethasone dipropionate 400mg/day administered for 12 weeks to paediatric patients with chronic asthma.
FLTB3014 Completed A multicenter, randomised, double-blind, double-dummy, parallel group clinical trial to determine the safety and efficacy of inhaled fluticasone propionate 500 mg bd metered dose inhaler with a Volumatic™ spacer compared to oral soluble prednisolone administered for 7 days to patients aged…
FLTB3015 Completed A multi-centre, randomized, double-blind, parallel-group clinical trial to compare the safety and efficacy of the dry powder formulation of fluticasone propionate 400mg/day and beclomethasone dipropionate 400mg/day administered for 52 weeks to paediatric patients with chronic asthma
FLTB3016 Completed A multi-centre, randomised, double-blind, placebo-controlled parallel group study to determine the efficacy and safety of inhaled fluticasone propionate 50mg bd and 100mg bd delivered via the Babyhaler™ spacer device in the management of asthma symptoms in children aged 12-47 months inclusive.
FLTB3017 Completed A multi-centre, randomised, double-blind, placebo-controlled parallel group study to determine the efficacy and safety of inhaled fluticasone propionate 100mg bd and 250mg bd delivered via the Babyhaler™ spacer device in the management of asthma symptoms in children aged 12–47 months inclusive.

 

 

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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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