A Confirmatory Study of KUC-7483 in Patients With Overactive Bladder
NCT01004315 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 750
Last updated 2010-07-27
Summary
To evaluate the efficacy and the safety of KUC-7483 in overactive bladder patients.
Conditions
Interventions
- DRUG
-
KUC-7483
- DRUG
- DRUG
-
Tolterodine
Sponsors & Collaborators
-
Kissei Pharmaceutical Co., Ltd.
lead INDUSTRY
Principal Investigators
-
Yasuhiro Omori · Clinical Development Department, Kissei pharmaceutical Co., Ltd.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- Japan
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