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Study ID Status Title Patient Level Data
113896 Completed PGx275 lapatinib liver safety pharmacogenetics in EGF30008
113898 Completed Outcomes Associated with Early or Delayed Maintenance Treatment Post-Chronic Obstructive Pulmonary Disease Exacerbation
113899 Completed Differences in the risk of re-hospitalization and other COPD-related (Chronic Obstructive Pulmonary Disease) exacerbations and costs for patients receiving fluticasone propionate-salmeterol xinafoate combination 250/50mcg (FSC) versus anticholinergics [i.e. tiotropium (TIO) and ipratropium or combination ipratropium-albuterol (IPR) post-hospitalization or ED visit for the treatment of COPD.
113900 Completed Clinical and Economic Burden of Patients with Chronic Obstructive Pulmonary Disease in a Medicaid Population
113901 Completed Outcomes for Chronic Obstructive Pulmonary Disease moderate exacerbators initiating treatment
113902 Completed Chronic Obstructive Pulmonary Disease (COPD)-Related Outcomes and Costs for Patients on Combination Fluticasone Propionate-Salmeterol Xinafoate 250/50mcg versus Anticholinergics in a Comorbid COPD-Depression/Anxiety Population
113903 Completed Observed outcomes associated with fluticasone propionate/salmeterol xinafoate or inhaled corticosteroids in asthma patients
113905 Completed An Open-Label, Flexible-Dose Study of Retigabine Immediate Release (IR) as Adjunctive Therapy to Specified Monotherapy Antiepileptic Treatments in Adults with Partial -Onset Seizures
113907 Completed Benefits of Adherence to 5-alpha reductase inhibitor treatment in Men with Enlarged Prostate: An Assessment of Medicare and Medicaid Patients Using the MarketScan Database
113908 Completed Clinical progression and costs in benign prostatic hyperplasia patients treated with early versus delayed combination therapy
113909 Completed Establishing the Benefits of Adherence to Enlarged Prostate Treatment: A Validation Study Linking Adherence to Outcomes Using the Market Scan Database
113913 Completed A Combination Product of Sumatriptan and Naproxen Sodium versus Single-entity Oral Triptans: An Analysis of Real World Data
113917 Completed Clinical and Economic Burden of Uncontrolled Epilepsy: Analyses from a Medicaid Database and a Private Health Plan Database
113918 Terminated Cost Analysis of Thrombocytopenia Treatment in Patients with Chronic Immune (Idiopathic) Thrombocytopenic Purpura
113922 Completed Outcomes Comparison of Chronic Immune Thrombocytopenic Purpura (ITP) Patients Switched to Eltrombopag and Romiplostim
113924 Withdrawn Immunogenicity and safety study of GSK Biologicals’ pandemic influenza (H1N1) candidate vaccine GSK2340274A in adults 18 to 64 years of age
113928 Active, not recruiting A Phase II study of the BRAF inhibitor dabrafenib as a single agent and in combination with the MEK inhibitor trametinib in subjects with BRAF V600E mutation positive metastatic (stage IV) non-small cell lung cancer
113929 Completed BRF113929: An Open-Label, Two-Cohort, Multicentre Study of GSK2118436 as a Single Agent in Treatment Naïve and Previously Treated Subjects with BRAF Mutation-Positive Metastatic Melanoma to the Brain
113932 Terminated Identification and characterization of the bacteria causing Acute Otitis Media (AOM) episodes in young children in Taiwan
113935 Completed Safety and immunogenicity of GSK Biologicals’ candidate tuberculosis vaccine (692342) when administered to HIV-positive adults living in a Tuberculosis endemic region
113939 Completed Relative bioavailability study between the formulations: Paroxetine 25 mg tablet with controlled release manufactured by GSK Mississauga and Paroxetine 25 mg tablets with controlled release manufactured by SmithKline Beecham (Cidra), fasted administration in healthy volunteers for both genders.
113946 Completed An open label, multi-centre, non-interventional post-marketing surveillance (PMS) to monitor the safety and effectiveness of HYCAMTIN administered in Korean patients according to the prescribing information
113948 Completed Safety and immunogenicity of new formulations of GlaxoSmithKline Biologicals’ DTPa-HBV-IPV/Hib vaccine (GSK217744) in primary infant vaccination
113949 Completed A partially blind study to evaluate the safety, reactogenicity and immunogenicity of GSK Biologicals’ Staphylococcal 4-component investigational vaccine (GSK2392102A) in healthy adults
113950 Completed A Single-Centre, Randomised, Open-label Study to Evaluate the Effects of Steady-State Verapamil, a Moderate P-Glycoprotein and CYP3A4 Inhibitor, on the Pharmacokinetics of GSK573719 and GSK573719 in Combination with GW642444 Study Listed on ClinicalStudyDataRequest.com

 

 

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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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