Overview
Safety and Efficacy of MK0594 to Treat Overactive Bladder (0594-003)
Status:
Completed
Completed
Trial end date:
2007-09-24
2007-09-24
Target enrollment:
0
0
Participant gender:
All
All
Summary
This study is designed to investigate whether a new drug may offer safe and effective treatment for patients with overactive bladder.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Merck Sharp & Dohme Corp.
Vyne Therapeutics Inc.
Criteria
Inclusion Criteria:- Patients with predominantly urge incontinence overactive bladder episodes
- Patients must meet minimum eligibility requirements (e.g., average number of
micturitions/day) based on screening diary cards
Exclusion Criteria:
- History of Diabetes insipidus, uncontrolled hyperglycemia or hypercalcemia
- Lower urinary tract symptoms associated with benign prostatic hypertrophy
- Active or current Urinary Tract Infections (UTIs)
- Surgery to correct prolapsed uterus or stress incontinence