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

NCT ID: NCT02658448

Last Updated: 2021-02-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 19 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-01-31
• Study Completion Date: 2018-06-30

Brief Summary

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.

Conditions

Stress Urinary Incontinence

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

GTx-024 3 mg

GTx-024 softgel capsules will be administered once daily to a total dose of 3 mg for up to 12 weeks.

Group Type: EXPERIMENTAL

GTx-024

Intervention Type: DRUG

GTx-024 softgel capsules will be administered once-daily to a total dose of 3 mg

Interventions

GTx-024

GTx-024 softgel capsules will be administered once-daily to a total dose of 3 mg

Intervention Type: DRUG

Other Intervention Names

enobosarm

Eligibility Criteria

Inclusion Criteria

• 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

Exclusion Criteria

• 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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

GTx

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kenneth M. Peters, MD

Role: PRINCIPAL_INVESTIGATOR

William Beaumont Hospitals

Locations

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

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

G201001

Identifier Type: -

Identifier Source: org_study_id