Viewing Study NCT00337090



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00337090
Status: COMPLETED
Last Update Posted: 2013-07-02
First Post: 2006-06-14

Brief Title: A Study of YM178 in Patients With Symptomatic Overactive Bladder DRAGON
Sponsor: Astellas Pharma Inc
Organization: Astellas Pharma Inc

Study Overview

Official Title: A Randomized Double-blind Parallel Group Placebo and Active Controlled Multicenter Dose Ranging Study With the Beta-3 Agonist YM178 in Patients With Symptomatic Overactive Bladder
Status: COMPLETED
Status Verified Date: 2013-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study will examine which dose of YM178 is best in terms of efficacy safety and tolerability compared to placebo and compared to tolterodine a marketed product
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None