The purpose of this study is to evaluate the efficacy and safety of TAS-303 in female
patients with stress urinary incontinence.
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Full eligibility criteria for NCT02906683
Ages eligible for Study
20 Years to 79 Years
Genders eligible for Study
Accepts Healthy Volunteers
Patient has symptoms of Stress Urinary Incontinence (SUI) for at least 12 weeks prior to study entry
Patient has at least 1 incontinence episodes per day, and urinary diurnal frequency of 10 or less per day and nocturia of 2 or less per day.
Patient is positive in 1-hour pad weight test
Patient has predominant or primary urge incontinence according to investigator judgment
Patient had a prior surgical SUI treatment
Patient is diagnosed stageII or more of Pelvic Organ Prolapse
Patient has symptoms of Urinary tract infection (UTI)
Patient is positive pregnancy test
Patient has on physical examination, neurological and/or vaginal examination results which, in the opinion of the investigator, should exclude the subject.
All locations for NCT02906683
Taiho Pharmaceutical Co., Ltd selected site
View full eligibility
Tris trial is registered with FDA with number: NCT02906683. The sponsor of the trial is Taiho Pharmaceutical Co., Ltd. and it is looking for 256 volunteers for the current phase.
Official trial title: A Phase IIa Study of TAS-303 in Female Patients With Stress Urinary Incontinence
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