A Phase II Study of KUC-7483 in Patients With Overactive Bladder
NCT00742833 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 400
Last updated 2009-09-04
Summary
To investigate the efficacy and safety of KUC-7483 in overactive bladder patients.
Conditions
- Overactive Bladder (OAB)
Interventions
- DRUG
-
KUC-7483
- DRUG
Sponsors & Collaborators
-
Kissei Pharmaceutical Co., Ltd.
lead INDUSTRY
Principal Investigators
-
Yasuhiro Omori · 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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