Found 13 matching trials
Exploratory Study of L.S.E.S.r. (LipidoSterolic Extract of Serenoa Repens)(PERMIXON® 160 mg Hard Capsule) Versus Tamsulosine LP Activity on Inflammation Biomarkers in Urinary Symptoms Related to BPH (Benign Prostatic Hyperplasia) PHASE4 Inflammation is reported as one of the most recent hypotheses to explain BP...
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Multiple Locations
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Safety and Efficacy of 0.5mg Dutasteride and 0.4mg Tamsulosin Combination Once Daily for Six Months for Benign Prostatic Hyperplasia PHASE4 Open-label, 6 month-treatment with the IP in all subjects. - Sample size: A...
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GSK Investigational Site
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Study to Evaluate the Bioequivalence of Astellas Phama Korea Inc. "Harnal-D" in Healthy Volunteers PHASE1 This study is an open-label, randomized, fasted, single dose, crossover stu...
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SECOTEX® (Tamsulosin Hydrochloride) Bioequivalence Study Brazil - Fast Admin PHASE1 It will be an open-label, randomized, laboratory-blind, crossover study wit...
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GSK Investigational Site
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Study to Evaluate the Bioequivalence of Astellas Phama Korea Inc. "Harnal-D" in Healthy Volunteers After Meal PHASE1 This study is an open-label, randomized, fed, single dose, crossover study ...
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PK Comparison of GL2701 With Finasteride and Tamsulosin in Combination PHASE1 To compare the relative bioavailability and pharmacokinetic characteristics...
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Clinical trial center of Anam Hospital
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SECOTEX® (Tamsulosin Hydrochloride) Bioequivalence Study Brazil - Fed Admin PHASE1 It will be an open-label, randomized, laboratory-blind, crossover study wit...
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GSK Investigational Site
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Clinical Study to Determine Bioequivalence of Oral Tamsulosin Products as 0.4 mg Prolonged-release Tablets in Male Subjects Under Fed Conditions NA Prospective, longitudinal, single-dose, randomized, open-label, crossover 2...
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Axis Clinicals Latina, S.A. de C.V.
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A Study to Evaluate the Safety and Pharmacokinetics of AD-116 and AD-1161 in Healthy Adult Male Subjects PHASE1 A Study to Evaluate the Safety and Pharmacokinetics of AD-116 and AD-1161 U...
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H PLUS YANGJI HOSPITAL, Seoul
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Clinical Study to Determine Bioequivalence of Oral Tamsulosin Products as 0.4 mg Prolonged-release Tablets in Male Subjects Under Fasted Conditions NA Prospective, longitudinal, single-dose, randomized, open-label, crossover 2...
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Axis Clinicals Latina, S.A. de C.V.
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