Postmenopausal with Urinary Incontinence
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- STATUS
- Recruiting
Summary
Postmenopausal with Urinary Incontinence
Description
This study is to compare the efficacy of study drug, Enobosarm, administered once daily to that of placebo by evaluating the number of subject reported stress incontinence episodes per day.
Volunteers will receive compensation for time, travel and study-related medical care. Qualified participants may receive study medications and all study related care including physical examinations and laboratory services at no cost. No medical insurance is necessary to participate.
Details
| Clinical Study Identifier | TX152090 |
|---|---|
| Last Modified on | 25 March 2021 |
How to participate?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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