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This is a placebo-controlled, double-blind study to evaluate the safety and efficacy of two doses of DR-3001 in women with overactive bladder who have symptoms of predominant or pure urge incontinence...
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Lead Sponsor
Duramed Research
NCT06885931 · Mixed Urinary Incontinence, Stress Urinary Incontinence (SUI), and more
NCT05989646 · Urinary Incontinence, Daytime Wetting, and more
NCT06798311 · Urinary Incontinence (UI), Lower Urinary Tract Symptoms (LUTS), and more
NCT07489794 · Multiple Sclerosis, Urinary Incontinence (UI)
NCT05362292 · Urinary Incontinence, Urge, Urinary Incontinence, and more
Duramed Investigational Site
Birmingham, Alabama
Duramed Investigational Site
Huntsville, Alabama
Duramed Investigational Site
Mobile, Alabama
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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