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Clinical Trial Summary

To investigate the long-term safety, efficacy and pharmacokinetics of KUC-7483 in patients with overactive bladder.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01003405
Study type Interventional
Source Kissei Pharmaceutical Co., Ltd.
Contact
Status Withdrawn
Phase Phase 3

See also
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