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Study ID Status Title Patient Level Data
117365 Completed PGx6652: Genetic Evaluation of Pazopanib –Related Hepatotoxicity
117374 Active, Not Recruiting PGx6633: FLAIR (GSK2190915) ADME Replication, Exploring the roles of UGT1A1 and UGT1A3
117375 Active, Not Recruiting HO-12-9141 SLS in-depth exit interviews on patient centered outcomes in COPD and asthma
117380 Completed A Phase I, Open-Label, Parallel-Group, Two-Part Study to Evaluate the Pharmacokinetics and Safety of GSK2336805 in Subjects with Hepatic Impairment and Healthy Matched Control Subjects (HAI117380)
117392 Completed PGx: Exploratory Analysis of Whole Bacterial Genome DNA Sequences of Escherichia coli Isolates from Two Patients Enrolled in the LRS114688 PhII cUTI Clinical Study
117393 Active, Not Recruiting PGx6557: Targeted Genotyping in lapatinib DILI positive re-challenge cases from EGF106708 and EGF106903
117394 Active, Not Recruiting Exploratory PGx Analysis of ALT elevation in EGF105485
117395 Active, Not Recruiting PGx6470: Genetics of Mepolizumab (SB240563) Treatment Response in Severe Asthmatics in MEA112997
11UK Completed Comparison of the effects of bupropion, dextroamphetamine and amitriptyline on human performance tests, autonomic responses, EEG and subjective rating scales.
120008/901 Completed A Study to Evaluate the Effect of a High Fiber and a High Fat Meal on the Pharmacokinetics of LANOXIN† (digoxin) Elixir Pediatric in Healthy Adults Study Listed on ClinicalStudyDataRequest.com
123(H73)-013-V Completed The Pharmacokinetics of Valaciclovir and Acyclovir After Oral Administration of a Single Dose of Valaciclovir to Patients With Cirrhosis and Healthy Volunteers
123-007 Completed A Comparative Trial of Valaciclovir and Aciclovir for the Suppression of Ano-Genital Herpes Infections in HIV-Infected Patients
123-008 Completed A Study to Investigate the Efficacy and Safety of Valaciclovir in the Treatment of Recurrent Ano-Genital Herpes in HIV-Infected Patients
123-014 Completed A Randomised Double-Blind Trial of Valaciclovir (BW256U87) Prophylaxis for Opportunistic Cytomegalovirus End-Organ Disease in Patients With Advanced HIV Infection (<100CD4+ Lymphocytes)
123-016 Completed 123-016: A Double-blind, Multi-centre Study Comparing Oral Valaciclovir and Aciclovir for the Suppression of CMV Infection and Disease Following Allogeneic Bone Marrow Transplantation
123-026 Completed A Comparative Trial of Valaciclovir With Aciclovir and Placebo for the Suppression of Recurrent Genital Herpes Infections in Immunocompetent Patients
123-031 Completed A Pilot, Randomized, Double-Blind Study to Investigate the use of Valaciclovir for the Prophylaxis of CMV Infection in Recipients of a Heart or Single Lung Transplant
123-033 Completed A randomized, double blind, placebo controlled cross over trial to compare valacyclovir HCl and acyclovir for suppression of subclinical herpes simplex virus sheddingExtensive searching has revealed that no clinical study report is available for this study.
123-034 Completed Report of the Pharmacokinetics of Aciclovir and Digoxin Following Administration of Digoxin and Valaciclovir Alone and in Combination to Healthy Volunteers
123-037 Completed A Randomised, Double-Blind, Controlled Study of Valaciclovir for the Suppression of Recurrent Genital Herpes Simplex Virus Infection in Immunocompetent Patients
123-038 Completed Evaluation of the Effect of an Aluminium Hydroxide and Magnesium Hydroxide Containing Antacid on the Pharmacokinetics of Valaciclovir and Acyclovir Following a Single Oral Dose of Valaciclovir
123-044 Completed Pharmacokinetics of valaciclovir in late pregnancy
123-304 Completed Zoster ophthalmicus in immunocompetent patientsExtensive searching has revealed that no clinical study report is available for this study. The clinical trial results were reported via publication. See citation below.
123-310 Completed A double-blind, multicenter study comparing valacyclovir HCL with famciclovir for the treatment of uncomplicated herpes zoster in immunocompetent patients 50 years of age and olderExtensive searching has revealed that no clinical study report is available for this study.
13 Completed Ninety-eight day, parallel, double-blind, randomized comparison of placebo, bupropion and amitriptyline (75-200mg/day) in outpatients, ages 55 and older – Extensive searching has revealed that no clinical study report is available for this study.

 

 

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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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