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Study ID Status Title Patient Level Data
ARI30015 Completed Multicentre, randomized, placebo-controlled, double-blind, parallel-group, phase IIIB clinical trial evaluating the efficacy of dutasteride in the prevention of bleeding related to prostate transurethral resection in subjects presenting with BPH.
ARI30016 Completed A long-term extension study of GI198745 in patients with Benign Prostatic Hyperplasia
ARI40001 Completed A multicentre, randomised, double-blind, double-dummy, parallel group study to compare the efficacy of GI198745 0.5mg Once Daily versus finasteride 5mg Once Daily for 12 months in the treatment of subjects with benign prostatic hyperplasia (BPH). (EPICS) Study Listed on ClinicalStudyDataRequest.com
ARI40001_1 Completed A Multicentre, Randomised, Double-Blind, Double-Dummy, Parallel-Group Study to Compare the Efficacy of Dutasteride/GI198745 0.5mg Once Daily Versus Finasteride 5mg Once Daily for 12 Months in the Treatment of Subjects with Benign Prostatic Hyperplasia (BPH), Followed by an Optional 24 Months Open Label Phase. Study Listed on ClinicalStudyDataRequest.com
ARI40002 Completed A pilot multi-centre, double-blind, parallel group, randomised study to investigate the effect on symptoms 3 months after discontinuing tamsulosin, following 6 months combination treatment with 0.5mg GI198745 and 0.4mg tamsulosin daily in patients with symptomatic Benign Prostatic Hyperplasia (BPH). Study Listed on ClinicalStudyDataRequest.com
ARI40005 Completed A randomized, double-blind, parallel group study to investigate the efficacy and safety of treatment with dutasteride (0.5mg) and tamsulosin (0.4mg), administered once daily for 4 years, alone and combination, on the improvement of symptoms and clinical outcome in men with moderate to severe symptomatic benign prostatic hyperplasia Study Listed on ClinicalStudyDataRequest.com
ARI40006 Completed A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study of the Efficacy and Safety of Dutasteride 0.5 mg Administered Orally Once Daily for Four Years to Reduce the Risk of Biopsy-Detectable Prostate Cancer Study Listed on ClinicalStudyDataRequest.com
ARI40007 Completed A Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study Investigating the Effects of Either 4 or 6 Weeks Dutasteride 0.5mg Daily on Peri-Operative Bleeding Following Transurethral Resection of the Prostate (TURP) in Subjects with Benign Prostatic Hyperplasia (BPH). Study Listed on ClinicalStudyDataRequest.com
ARI40010 Completed Multicenter, double-blind, randomized, parallel-group study, comparing 0.5 mg and 3.5 mg dutasteride daily for 4 months prior to radical prostatectomy versus radical prostatectomy alone in men with biopsy-proven and clinically localized prostate cancer Study Listed on ClinicalStudyDataRequest.com
ARI40013 Completed GI 198745 in the Treatment of Symptomatic Benign Prostatic Hyperplasia (BPH): An Open, Multicentre, Phase IIIb Study.
ARI40014 Completed Effects of Dutasteride on Intraprostatic Dihydrotestosterone (DHT) Levels Study Listed on ClinicalStudyDataRequest.com
ARIA1001 Completed An Investigation of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GI198745 (dutasteride), an Inhibitor of the 5-Alpha Reductase Enzyme, In Healthy Adult Males
ARIA1002 Completed A pilot investigation of the relative bioavailability of oral formulations of GI198745 (dutasteride), an inhibitor of the 5-alpha reductase enzyme, in healthy adult male volunteers
ARIA1003 Completed An Investigation of the Safety, Tolerability Pharmacokinetics and Pharmacodynamics of DUT(/dutasteride) When Administered Daily for 28 Days in Patients with Benign Prostatic Hyperplasia
ARIA1004 Completed An Evaluation of the Relative Bioavailability of the GI198745 (Dutasteride) Soft Gelatin Capsule with Monodiglycerides of Caprylic/Capric Acid (MDC) in Healthy Adult Male Volunteers
ARIA1007 Completed The Effects of Aging on the Pharmacokinetic and Pharmacodynamic Characteristics of GI198745/Dutasteride in Healthy Adult Male Volunteers
ARIA1009 Completed An Investigation of the Pharmacokinetics of GI198745 and of the Effects of GI198745 on Semen Characteristics When Administered Daily for 12 Months to Healthy Male Subjects Study Listed on ClinicalStudyDataRequest.com
ARIA1010 Completed An Evaluation of the Effects of Cholestyramine on the Pharmacokinetics of GI198745(Dutasteride)
ARIA1011 Completed An Open-label, Crossover Study to Investigate the Pharmacokinetic-Pharmacodynamic Interaction Between (1) Tamsulosin and GI198745(dutasteride) and (2) Terazosin and GI198745 (dutasteride) When Co-administered to Healthy Male Subjects for 14 Days
ARIA1012 Completed Investiagtion of the Metabolic Fate and Routes of Excretion of GI198745 at Steady State in Healthy Male Subjects Study Listed on ClinicalStudyDataRequest.com
ARIA2001 Completed A Double-Blind, Placebo-Controlled, Dose-Ranging, Clinical Evaluation of GI198745 and Finasteride in Subjects with Benign Prostatic Hyperplasia.
ARIA2003 Completed A Randomized, Double-Blind, Placebo-Controlled Pilot Study to Evaluate the Safety And Preliminary Efficacy of Neoadjuvant Therapy With GI198745 in Subjects With Localized Prostate Cancer Undergoing Radical Prostatectomy. Study Listed on ClinicalStudyDataRequest.com
ARIA2004 Completed A Double-Blind, Placebo-Controlled, Dose-Ranging Clinical Evaluation of GI198745 and Finasteride in Subjects with Androgenetic Alopecia
ARIA3001_1 Completed A Randomized, Double-Blind, Placebo-Controlled, Two Year Parallel Group Study of the Efficacy and Safety of Dutasteride GI198745 0.5mg in the Treatment and Prevention of Progression of Benign Prostatic Hyperplasia, Followed by a Two-Year Open-Label Treatment Phase (Report on Year 1 Data) Study Listed on ClinicalStudyDataRequest.com
ARIA3001_2 Completed A Randomized, Double-Blind, Placebo-Controlled, Two Year Parallel Group Study of the Efficacy and Safety of dutasteride GI198745 0.5mg in the Treatment and Prevention of Progression of Benign Prostatic Hyperplasia, Followed by a Two-Year Open-Label Treatment Phase (Report on 2 Year Data). Study Listed on ClinicalStudyDataRequest.com

 

 

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