This Was a Multinational Study Comparing the Efficacy and Safety of Two Medicines , Solifenacin Succinate and Mirabegron Taken Together, or Separately, or a Mock Treatment (Placebo) in Subjects With Symptoms of Overactive Bladder



Status:Completed
Conditions:Overactive Bladder, Urology
Therapuetic Areas:Gastroenterology, Nephrology / Urology
Healthy:No
Age Range:18 - Any
Updated:11/3/2018
Start Date:November 5, 2013
End Date:October 22, 2015

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A Randomized, Double-Blind, Parallel-Group, Placebo- and Active-Controlled, Multi-center Study to Evaluate the Efficacy, Safety and Tolerability of Combinations of Solifenacin Succinate and Mirabegron Compared to Solifenacin Succinate and Mirabegron Monotherapy in the Treatment of Overactive Bladder

The purpose of this study was to examine how well two medicines (solifenacin succinate and
mirabegron) combined work compared to each medicine alone in the treatment of bladder
problems.


Inclusion Criteria:

- Subject was willing and able to complete the micturition diary and questionnaires
correctly and able to measure his/her vital signs at home at stipulated time points,
using the device provided by the study personnel, and to adequately record the
readings;

- Subject had symptoms of "wet" OAB (urinary frequency and urgency with incontinence)
for at least 3 months;

Exclusion Criteria:

- Subject had significant PVR volume (> 150 mL);

- Subject had a neurological cause for detrusor overactivity (e.g. neurogenic bladder,
diabetic neuropathy with autonomic component or bladder involvement, or systemic or
central neurological disease such as multiple sclerosis and Parkinson's disease with
autonomic component or bladder involvement). An autonomic component could be inferred
when autonomic functions were affected, including heart rate, blood pressure,
perspiration and digestion.

- Subject had an indwelling catheter or practices intermittent self catheterization.

- Subject had chronic inflammation such as bladder pain syndrome /interstitial cystitis,
symptomatic bladder stones or any previous or current radiation cystitis.

- Subject had received intravesical treatment in the past 12 months with e.g., botulinum
toxin, resiniferatoxin, capsaicin.

- Subject had moderate to severe hepatic impairment

- Subject had severe renal impairment

- Subject had a clinically significant abnormal ECG

- Subject had a concurrent malignancy or history of cancer (except noninvasive skin
cancer) within the last 5 years prior to screening.

- Subject had an average QTcF interval > 450 ms for males or > 470 ms for females based
on the triplicate ECGs completed at Screening or is at risk of QT prolongation (e.g.,
family history of long QT syndrome, hypokalaemia).

- Subject had severe hypertension, which is defined as a sitting average systolic blood
pressure ≥ 180 mmHg and/or average diastolic blood pressure ≥ 110 mmHg.
We found this trial at
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Walla Walla, Washington 99362
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