To evaluate the safety and efficacy of solifenacin succinate in subjects with overactive bladder symptoms (urgency, with or without urge incontinence, usually with frequency and nocturia).
Study included a 24 week extension that did not occur due to FDA approval of the product.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
2,225
oral
To evaluate the efficacy of 5 and 10mg solifenacin succinate in patients with OAB symptoms
Time frame: Weeks 4, 8 and 12
Percentage of patients satisfied with 5mg treatment
Time frame: Week 12
Percentage of patients obtaining additional benefit with increase to 10mg dose
Time frame: week 12
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Bay Minette, Alabama, United States
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Birmingham, Alabama, United States
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Birmingham, Alabama, United States
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Birmingham, Alabama, United States
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Decatur, Alabama, United States
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Huntsville, Alabama, United States
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Oro Valley, Arizona, United States
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Phoenix, Arizona, United States
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Phoenix, Arizona, United States
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Scottsdale, Arizona, United States
...and 188 more locations