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Study ID Status Title Patient Level Data
ESS40002 Completed A 96-Week, Randomized, Open-Label, Multi-center Trial to Evaluate the Safety and Tolerability of the Antiretroviral Activity of Stavudine (40mg bid) + Lamivudine (150mg bid) + Nelfinavir (1250mg bid) Versus Abacavir (300mg bid) + COMBIVIR (3TC 150mg/ZDV 300mg bid) Versus COMBIVIR (3TC 150mg/ZDV ...
ESS40003 Completed Randomized, Multicenter, Open-Label Trial to Evaluate the Reversibility of Dyslipidemia upon Substitution of Abacavir for a Protease Inhibitor in Virologically Controlled HIV (+) Subjects with Elevated Cholesterol.
ESS40005 Completed A Phase IIIB Randomized, Multi-center Study of the Efficacy and Safety of COMBIVIR 1 Tablet PO BID Plus ZIAGEN 300mg PO BID Versus an Abacavir 300mg/Lamivudine 150mg/Zidovudine 300mg Combination Tablet PO BID, Administered for 24 Weeks in Subjects With HIV-1 Infection
ESS40006 Completed A Phase II, Randomized, Open-Label Comparative, Pilot Study of Two Different Dosage Regimens of Amprenavir (600 mg BID vs. 900 mg BID) in Combination with Ritonavir (100 mg BID) Plus Abacavir, Another NRTI, and Either Efavirenz or Tenofovir DF in HIV-1 Infected Subjects with Virologic Evidence o ...
ESS40009 Completed A Phase IV, Open-Label Study to Assess the Safety and Tolerability of Abacavir (Ziagen) in HIV-1 Infected Individuals and to Investigate the Effect of Baseline Genotype with Virtual Phenotype on the Response to Abacavir in Therapy Experienced Subjects in the Clinical Setting
ESS40010 Completed ESS40010, Trial to Assess the Regression of Hyperlactatemia and to Evaluate the Regression of Established Lipodystrophy in HIV-1-Positive Subjects (TARHEEL)
ESS40011 Completed A 24-week, Randomized, Open-Label, Multicenter Trial to Compare the Safety and Efficacy of the Licensed AGENERASE Dose (1200mg BID) to a Lower AGENERASE Dose (600mg BID) in the Presence of Norvir (100mg BID) when Combined with Other Background Antiretroviral Drugs in HIV-1 Infected Subjects.
ESS40013 Completed A Phase IV Multi-center Study of the Efficacy and Safety of 48-Week Induction Treatment with TRIZIVIR (Abacavir 300mg/Lamivudine 150mg/Zidovudine 300mg Combination Tablet BID) + Efavirenz (600mg QD) Followed by 48-Week Randomized, Open-Label, Maintenance Treatment with TRIZIVIR…
ESZ111503 Completed A randomised, double-blind, double-dummy, placebo-controlled, 3-way crossover study to evaluate potential next-day residual effects of a single evening dose of 3mg eszopiclone and 7.5mg zopiclone in healthy adult subjects.
FAP10001 Completed Dose proportionality of fluticasone propionate from HFA inhalers and effect of propellant on FP pharmacokinetics Study Listed on ClinicalStudyDataRequest.com
FAP10006 Completed A Randomized, Open-Label, 2-Way Crossover, Repeat-Dose Study in Pediatric Subjects with Asthma, Age 4-11 Years, to Compare Systemic Exposure of Fluticasone Propionate 2x44mcg Following Administration by Metered-Dose Inhalers Containing Hydrofluoroalkane or Chlorofluorocarbon Propellants Study Listed on ClinicalStudyDataRequest.com
FAP19052 Completed Pharmacodynamics of the 88mcg BID dose of the Hydrofluoroalkane propellant formulation of inhaled Fluticasone Propionate following Administration via the Metered-dose Inhaler in Pediatric Subjects 4 to 11 years of age with Asthma Study Listed on ClinicalStudyDataRequest.com
FAP19058 Completed Systemic exposure of the fluticasone propionate from the hydrofluoroalkane propellant formulation via the metered-dose inhaler with and without a spacer in pediatric subjects 4 to 11 years of age with asthma. Study Listed on ClinicalStudyDataRequest.com
FAP30001 Completed A Randomized, Double-Blind, Parallel-Group Trial of Inhaled Fluticasone Propionate/GR106642X 220mcg BID and 440mcg BID in Adolescent and Adult Subjects with Asthma
FAP30007 Completed A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled 12-Week Trial of Inhaled Fluticasone Propionate 88mcg BID, 220mcg BID, and 440mcg BID versus Placebo in Propellant GR106642X in Adolescent and Adult Subjects with Asthma who are Maintained on Inhaled Corticosteroid Therapy Study Listed on ClinicalStudyDataRequest.com
FAP30008 Completed A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled 12-Week Trial of Inhaled Fluticasone Propionate 88mcg BID, 220mcg BID, and 440mcg BID versus Placebo in Propellant GR106642X in Adolescent and Adult Subjects with Asthma who are Maintained on Bronchodilator Therapy Study Listed on ClinicalStudyDataRequest.com
FAP30010 Completed A Randomized, Double-Blind, Paralled-Group, Placebo-Controlled 12 Week Trial of Inhaled Fluticasone Propionate 88mcg Twice Daily versus Placebo in Propellant GR106642X in Pediatric Subjects 4 to 11 years of age with Asthma Study Listed on ClinicalStudyDataRequest.com
FAP30011 Completed A multi-centre, randomised, double-blind, parallel group clinical trial to assess the efficacy and safety of fluticasone propionate/GR106642X 250mg BD compared with fluticasone propionate/propellants CFC 250mg BD administered by pressurised metered-dose inhaler in adult Chinese patients with asthma.
FAS10002 Completed A multiple-dose, open-label, 2-way crossover study in pediatric subjects with asthma aged 1 to < 4 years to compare the systemic exposure of fluticasone propionate 88mcg administered via the hydrofluoroalkane metered-dose inhaler using the valved holding chambers, Aerochamber Plus™ and Babyhaler™, with face-masks Study Listed on ClinicalStudyDataRequest.com
FAS106533 Completed PD of Hydrofluoroalkane propellant of inhaled fluticasone propionate following administration in pediatric subjects 6-12 months of age with asthma Study Listed on ClinicalStudyDataRequest.com
FAS30006 Completed A Multicentre, Randomised, Double-Blind, Parallel Group Clinical Trial to Compare the Efficacy and Safety of Fluticasone propionate (FP) 200mg/day with Fluticasone propionate 400mg/day Administered for 52 Weeks via a Multidose Powder Device (Diskus) to Paediatric patients with Asthma.
FAS30007 Completed A multicentre, randomised, double-blind, parallel group placebo-controlled study to determine the efficacy and safety of fluticasone propionate 200mcg/day delivered via the Babyhaler in paediatric subjects aged 12 to 47 months with recurrent/persistent asthma like symptoms. Study Listed on ClinicalStudyDataRequest.com
FAS30009 Completed A multicentre, randomised, parallel-group open label study to assess the long term safety of fluticasone propionate 100mcg bd via the MDI and babyhaler spacer device, compared with sodium cromoglycate 5mg QDS in children aged 12-47months with documented evidence of recurrent/persistent asthma-like symptoms. Study Listed on ClinicalStudyDataRequest.com
FAS30030 Completed A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, 12-Week Safety and Efficacy Study of Fluticasone Propionate 88mcg BID Versus Placebo BID delivered via HFA MDI and a valved holding chamber with facemask in Pediatric Subjects with Asthma age 12 months to 47 months. Study Listed on ClinicalStudyDataRequest.com
FAS40008 Completed An interventional three year study for asthma control - In what way and in what kind of population is it possible to get asthmatic patients free from symptoms, keep the patients in work, restore a normal lung function, diminish hyperreactivity and normalise quality of life? Study Listed on ClinicalStudyDataRequest.com

 

 

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