A Study of Mirabegron (YM178) in Men With Lower Urinary Tract Symptoms (LUTS) and Bladder Outlet Obstruction (BOO)

Completed · Phase 2 · Has a placebo group

Conditions studied: Lower Urinary Tract Symptoms, Bladder Outlet Obstruction

In brief

This study examined the safety, tolerability, and efficacy of mirabegron (YM178) compared to placebo.

Key facts

Study ID

NCT00410514

Run by

Astellas Pharma Inc

People needed

200

Starts

2006-12-01

Expected to finish

2008-08-01

Last updated by the study team

2014-04-04

Who can join

Age: 45 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Men 45 years of age or older
• Documented bladder outlet obstruction

You may not qualify if…

• History of urinary retention
• Symptomatic and recurrent urinary tract infection (UTI)

Where it is running

• Study site — Tuscon, Arizona, United States
• Study site — Atherton, California, United States
• Study site — Culver City, California, United States
• Study site — Fresno, California, United States
• Study site — San Diego, California, United States
• Study site — Torrance, California, United States
• Study site — Middlebury, Connecticut, United States
• Study site — Tallahassee, Florida, United States
• Study site — Des Moines, Iowa, United States
• Study site — Shreveport, Louisiana, United States
• Study site — Watertown, Massachusetts, United States
• Study site — Garden City, New York, United States
• Study site — Winston-Salem, North Carolina, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Virginia Beach, Virginia, United States
• Study site — Victoria, British Columbia, Canada
• Study site — Victoria, British Columbia, Canada
• Study site — Winnipeg, Manitoba, Canada
• Study site — Saint John, New Brunswick, Canada
• Study site — Halifax, Nova Scotia, Canada
• Study site — Kitchener, Ontario, Canada
• Study site — Toronto, Ontario, Canada
• Study site — Chicoutimi, Quebec, Canada
• Study site — Chicoutimi, Quebec, Canada
• Study site — Montreal, Quebec, Canada

Full record on ClinicalTrials.gov

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