GTx-024 as a Treatment for Stress Urinary Incontinence in Women

Completed · Phase 2

Conditions studied: Stress Urinary Incontinence

In brief

The purpose of this study is to determine whether GTx-024 is safe and effective in the treatment of stress urinary incontinence in postmenopausal women.

Key facts

Study ID

NCT02658448

Run by

GTx

People needed

19

Starts

2016-01-01

Expected to finish

2018-06-01

Last updated by the study team

2021-02-01

Who can join

Age: 18 and older, up to 80. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Give voluntary, written and signed, informed consent
• Female
• Age18 to 80 years old be clinically confirmed as postmenopausal. Subjects must have undergone the onset of spontaneous, medically induced or surgical menopause prior to the start of this study. Spontaneous menopause is defined as 12 months of spontaneous amenorrhea or 6 months of spontaneous amenorrhea with serum FSH levels > 40 mIU/ml or 6 weeks postsurgical bilateral oophorectomy with or without hysterectomy
• SUI symptoms for at least 6 months duration
• Predominant SUI (MESA questionnaire)
• 24 hour pad weight >3 gms at baseline
• A minimum of 1 SUI episode per day, in the 3 day diary
• 3-15 SUI episodes per day, averaged over 3 days, in the 3 day diary
• Serum AST and ALT within normal limits
• Total bilirubin within normal limits
• Positive Bladder Stress Test during screening
• Subject agrees to not start any new treatment (medication or otherwise) that is known to affect lower urinary tract function throughout the treatment and follow up periods
• Subject agrees to maintain on a stable dose of any medication known to affect lower urinary tract function, including but not limited to anticholinergics, tricyclic antidepressants, or alpha-adrenergic blockers, throughout the treatment and follow-up period

You may not qualify if…

• Pelvic floor physical therapy in a clinical setting within 30 days prior to screening
• History of pelvic radiation treatment
• History of urethral diverticula
• History of urethral sling, anterior prolapse repair, ureteral bulking agents and/or other SUI procedure or surgery
• Known vesicoureteral reflux, vaginal prolapse beyond the introitus, or other significant urological findings, including pelvic floor abnormalities which, in the judgement of the investigator, could impact treatment
• Urinary incontinence of neurogenic etilogy
• Patient is morbidly obese (defined as 100 pounds over their ideal body weight, or body mass index 40 or greater)
• Chronic hepatitis
• Hepatic cirrhosis
• HIV and/or hepatitis A, B, or C
• Subjects taking systemic hormone products
• Subjects with a history of breast or endometrial cancer
• Myocardial infarction or arterial thromboembolic events within 6 months prior to Baseline, severe or unstable angina, New York Heart Association (NYHA) Class III or IV disease, serious uncontrolled cardiac arrhythmia grade II or higher according to NYHA, uncontrolled hypertension (systolic > 150 and/or diastolic > 100 mm Hg)
• Subjects with an entry measurement of > 5 mm endometrial stripe thickness
• Clinically confirmed urinary tract infection
• Any other condition which per investigators' judgment may increase subject risk

Where it is running

• William Beaumont Hospital — Royal Oak, Michigan, United States
• Urologic Consultants of Southeastern Pennsylvania — Bala-Cynwyd, Pennsylvania, United States
• Penn Center for Continence and Pelvic Health, University of Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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