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Study ID Status Title Patient Level Data
116364 Completed Study FFR116364, a double-blind, placebo-controlled study of GW685698X in paediatric subjects with perennial allergic rhinitis Study Listed on ClinicalStudyDataRequest.com
116365 Completed Study FFR116365, an open-label study of GW685698X in paediatric subjects with perennial allergic rhinitis Study Listed on ClinicalStudyDataRequest.com
116371 Completed A Phase 1, Open-Label, Crossover Study to Demonstrate the Bioequivalence of RYTHMOL SR® (propafenone hydrochloride) Manufactured at Two Different Sites Study Listed on ClinicalStudyDataRequest.com
116378 Completed A Single Blind (Sponsor-unblinded), Placebo-controlled, Parallel-group Study to Investigate the Efficacy and Safety of GSK1070806 in the Treatment of Obese Subjects with T2DM. Study Listed on ClinicalStudyDataRequest.com
116387 Completed Epidemiological multinational (Russia, Ukraine and Kazakhstan), retrospective observational study to evaluate medical, economic and social factors in patients with systemic lupus erythematosus in heading rheumatologic centers
116389 Completed GSK2302032A Antigen-Specific Cancer Immunotherapeutic as adjuvant therapy in patients with Non-Small Cell Lung Cancer Study Listed on ClinicalStudyDataRequest.com
116392 Completed A randomized, double blind, placebo-controlled study to investigate the safety and pharmacodynamics of repeat intranasal administration of the TLR7 agonist GSK2245035 in subjects with respiratory allergies Study Listed on ClinicalStudyDataRequest.com
116402 Completed A multi-national, randomized, double-blind, placebo-controlled, 3-period crossover study with GSK 573719 as monotherapy in adult subjects with asthma Study Listed on ClinicalStudyDataRequest.com
116404 Completed Sleepiness and mood in Parkinson's disease and combination treatment with ropinirole and levodopa
116406 Completed A study to test the possibility of cross reaction of the antibodies induced by the ELAPRASE (R) to GSK2788723 ELAPRASE is a trade mark owned by a third party
116409 Completed An open-label, randomised, cross-over, single centre study in healthy volunteers to optimise the Rotacap formulation andROTAHALER device for delivery of Fluticasone propionate/salmeterol.
116415 Completed A randomized, double-blind, single dose, four way cross-over study to assess the systemic exposure, systemic pharmacodynamics and safety and tolerability of FluticasoneFuroate, Umeclidinium and Vilanterol following single inhaled doses of Umeclidinium/Vilanterol blend + Fluticasone Furoate, Umeclidinium + Vilanterol, Fluticasone Furoate + Vilanterol and Fluticasone Furoate + Umeclidinium in healthy subjects Study Listed on ClinicalStudyDataRequest.com
116416 Completed Single and Repeat Dose Pharmacokinetic Study of GSK1605786 in Healthy Chinese Subjects Study Listed on ClinicalStudyDataRequest.com
116427 Completed An observer-blind study to evaluate immunogenicity and safety of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A in adults 18 years of age or older with solid tumours receiving chemotherapy
116428 Completed Study to evaluate safety and immunogenicity of GSK Biologicals' Herpes Zoster vaccine GSK1437173A in adults aged 18 years and older with haematologic malignancies
116429 Completed Prospective cohort study for patients’ adherence on lower urinary tract symptoms (LUTS) / Benign prostatic hyperplasia (BPH) pharmacological treatment in real practice
116431 Completed An Open-Label Study to Determine the Safety and Pharmacokinetics of AT1001 in Subjects with Impaired Renal Function and Healthy Subjects with Normal Renal Function (AT1001-015)
116435 Completed A Phase 1 Study to Investigate the Absorption, Metabolism and Excretion of [14C] AT1001 (migalastat hydrochloride) following a Single Oral Administration in Healthy Volunteers (AT1001-014)
116439 Completed A study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK2586184 following a single doseof 800mg and repeat oral tablet doses of 800mg b.d and the effect of food and gender on the pharmacokinetics of oralGSK2586184 in healthy subjects
116441 Completed Single Oral Dose Study of Atovaquone/Proguanil Hydrochloride Combination Tablets and Atovaquone Suspension. - A Single Oral Dose Study to Investigate Pharmacokinetics of Atovaquone and Proguanil from Combination Tablets and Atovaquone from Atovaquone Suspension in Japanese Healthy Males. -
116454 Active, Not Recruiting Special Drug Use Investigation for ReQuip® Controlled-Release (CR)
116455 Completed A Multi-Center, Open-labelled Study to Evaluate the Safety of Levocetirizine Hydrochloride Oral Solution in Children Aged 6 Months to 2 Years with Allergic Rhinitis or Pruritus Associated with the Skin Diseases.
116456 Recruiting A Post-Marketing Surveillance Study of Requip PD™ (Ropinirole) in the Treatment of Adult Filipino Patients diagnosed with Parkinson’s Disease
116457 Terminated An open-label extension study of the long-term safety, tolerability and efficacy of ambrisentan in subjects with inoperable chronic thromboembolic pulmonary hypertension (CTEPH)
116459 Completed Pharmacokinetic Study of Levocetirizine Oral Solution-An open-label, randomized, cross-over study to evaluate the pharmacokinetics, the safety and tolerability of levocetirizine oral solution (5 mg) and cetirizine dry syrup (10 mg), following a single dose in Japanese healthy male subjects-

 

 

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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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