Found 8 matching trials
Evaluate the Safety, Tolerability and PK of Different Formulations of Orally Administered Solabegron in Healthy Male Subjects PHASE1 The purpose of this study is to evaluate the safety, tolerability and pharm...
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Multiple Locations
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Dose Ranging Study Of Solabegron Versus Placebo In Female Patients With Overactive Bladder Symptoms PHASE2 This study will test the effectiveness and safety of two doses of solabegro...
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GSK Investigational Site
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A Study To Investigate The Effect Of Solabegron (GW427353) On Gastrointestinal Transit In Healthy Volunteers PHASE1 This study will test the hypothesis that GW427353, a beta-3 adrenergic agon...
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GSK Investigational Site
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A Two-Part Study to Determine: Best Medication Formulation and Food Effect PHASE1 This is a two-part study. Part 1 is designed to find the best modified rele...
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GSK Investigational Site
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A Study To Test The Interaction of Two Medications for Treatment of Overactive Bladder PHASE1 The purpose of this study is to determine the effect of repeat doses of sol...
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GSK Investigational Site
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A Study To Investigate GW427353 In Subjects With Irritable Bowel Syndrome (IBS) PHASE2 This study will test the hypothesis that GW427353, a beta-3 adrenergic agon...
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GSK Investigational Site
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Evaluation of the Efficacy and Safety of Solabegron Tablets for Treatment of Overactive Bladder in Adult Women PHASE2 This is a Phase 2b, multicenter, randomized, double-blind, placebo-controll...
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Velicept Investigative Site - Birmingham
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A Study to Evaluate Once Daily Low Dose and High Dose Solabegron or Placebo Given for 12 Weeks to Treat Women With Symptoms of Overactive Bladder: Sudden Urge to Urinate, Frequent Urination Associated With Wetting Episodes (VEL-2001) PHASE2 This is a Phase 2b, multicenter, randomized, double-blind, placebo-controll...
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Velicept Investigative Site - Birmingham
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