drugset / Trial / NCT02294396
Postmarketing Study to Evaluate add-on Therapy With Anticholinergics in Patients With Overactive Bladder (OAB) on Mirabegron.
RandomizedParallel-groupOpen-labelTreatment
Summary
The objective of the study was to evaluate the safety and efficacy of add-on therapy with anticholinergics in patients with OAB on mirabegron.
Timeline
- Start
- 2014-10-28
- Primary completion
- 2016-09-07
- Completion
- 2016-09-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Imidafenacin | Small molecule | 0.2 mg | Oral |
| Subject | Imidafenacin | Small molecule | 0.4 mg | Oral |
| Subject | Propiverine | Small molecule | 20 mg | Oral |
| Subject | Propiverine | Small molecule | 40 mg | Oral |
| Subject | Solifenacin | Small molecule | 5 mg | Oral |
| Subject | Solifenacin | Small molecule | 10 mg | Oral |
| Subject | Tolterodine | Small molecule | 4 mg | Oral |
| Background | Mirabegron | Other / unclassified | 50 mg | Oral |