Clinical trial
A Randomized, Double-Blind, Factorial, Parallel-Group, Active and Placebo-Controlled, Multicenter Dose-Ranging Study to Evaluate the Efficacy, Safety and Tolerability of Six Dose Combinations of Solifenacin Succinate and Mirabegron Compared to Mirabegron and Solifenacin Succinate Monotherapies in the Treatment of Overactive Bladder.
NCT01340027 is registered in ClinicalTrials.gov with Astellas Pharma Europe B.V. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomized, Double-Blind, Factorial, Parallel-Group, Active and Placebo-Controlled, Multicenter Dose-Ranging Study to Evaluate the Efficacy, Safety and Tolerability of Six Dose Combinations of Solifenacin Succinate and Mirabegron Compared to Mirabegron and Solifenacin Succinate Monotherapies in the Treatment of Overactive Bladder.
- Lead sponsor
- Astellas Pharma Europe B.V.
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- March 29, 2011
- Completion date
- June 28, 2012
- Enrollment
- 1,307 (actual)
- Sites
- 133
Conditions
As the registry lists them; a condition with its own page is linked.