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

No results posted yet for this study

Summary

To evaluate the efficacy and the safety of KUC-7483 in overactive bladder patients.

Conditions

Interventions

DRUG

KUC-7483

DRUG

Placebo

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01004315 on ClinicalTrials.gov