Title

Evaluation of the Efficacy and Safety of Silodosin in the Treatment of the Signs and Symptoms of BPH
Evaluation of the Efficacy and Safety of Silodosin vs. Tamsulosin and Placebo in the Treatment of the Signs and Symptoms of BPH. Multicentre, Randomised, Double-Blind, Controlled Trial With an Optional Long-Term, Open-Label Extension Phase.
  • Phase

    Phase 3
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Study Participants

    1228
A new drug for the treatment of benign prostatic hyperplasia is compared with placebo and tamsulosin (a drug belonging to the same therapeutic class) for to determine if it is safe and effective (the first phase of the study lasts approximately 18 weeks) and then is used for another 9 months to determine its long-term safety.
This is a multi-centre, double-blind, placebo and active controlled, parallel 12 week treatment trial in men with signs and symptoms of benign prostatic hyperplasia, followed by a 9 month open-label phase. The following procedures are used: physical exams, electrocardiograms, clinical laboratory tests, vital signs, the International Prostate Symptom Score, maximum urine flow rate, adverse events, concomitant medications, quality of life and compliance. 93 centres in 11 European countries (Finland, France, Germany, Italy, Netherlands, Poland, Romania, Russia, Spain, Ukraine, UK) will be involved
Study Started
May 31
2006
Primary Completion
May 31
2007
Study Completion
Jan 31
2008
Last Update
Feb 19
2009
Estimate

Drug Silodosin

8 mg daily for 12 weeks

  • Other names: KMD3213

Drug Tamsulosin

0.4 mg daily for 12 weeks

  • Other names: Omnic

Drug Placebo

once daily for 12 weeks

Silodosin Experimental

Tamsulosin Active Comparator

Placebo Placebo Comparator

Criteria

Inclusion Criteria:

Males in good general health and at least 50 years of age, with symptoms of moderate to severe Benign Prostatic Hyperplasia

Exclusion Criteria:

Medical conditions that would confound the efficacy evaluation
Medical conditions in which it would be unsafe to use an alpha-blocker
Use of concomitant drugs that would confound the efficacy evaluation
Use of concomitant drugs that would be unsafe with this alpha-blocker
No Results Posted