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NCT00527033 Clinical Trial

A Study of YM178 in Patients With Symptomatic Overactive Bladder

Urinary Bladder, Overactive Clinical Trial

Official title:
A Randomized, Double-blind, Parallel-group, Placebo-controlled Study in Patients With Symptomatic Overactive Bladder

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00527033
Other study ID # 178-CL-045
Secondary ID
Status Completed
Phase Phase 2
First received September 6, 2007
Last updated February 14, 2017
Start date September 2007
Est. completion date April 2008

Study information
Verified date February 2017
Source Astellas Pharma Inc
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Examine which dose of YM178 is the best in terms of efficacy, safety and tolerability compared to placebo

Description:

To investigate the dose-response relationship of YM178 in terms of efficacy, safety and tolerability, and also the superiority of YM178 over placebo.

Recruitment information / eligibility
Status Completed
Enrollment 842
Est. completion date April 2008
Est. primary completion date April 2008
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients over 20 years suffering from overactive bladder

Exclusion Criteria:

- Pregnant and breastfeeding women

- Any clinically significant abnormal conditions which in the opinion of the investigator makes the patient unsuitable for the study

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• YM178
Oral
• Placebo
Oral

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Astellas Pharma Inc

Country where clinical trial is conducted

Japan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Overactive bladder symptoms 12 weeks
Secondary Overactive bladder symptoms (QOL) 12 weeks
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