drugset / Trial / NCT00501371

MCS in Treating Lower Urinary Tract Symptoms (LUTS) Suggestive of Benign Prostatic Hyperplasia

NCT00501371 ↗

Phase 3 Terminated 85 enrolled Health Ever Bio-Tech Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Phase III, Randomized, double-blind, parallel placebo-controlled study. Two arms: MCS (30mg/day) vs. placebo. Subproject MCS-2: alpha-blocker naïve subjects Subproject MCS-3: subjects responding poorly to alpha-blocker

Timeline

Start
2007-07
Primary completion
2009-10
Completion
2009-10

Outcome

Outcome not reported

Stopped: “Study terminated for re-design. A new IND study (US FDA, July 2009) will be conducted in US and Taiwan. Termination not related to safety concerns.”

Drugs

EvaluationDrugModalityDoseRoute
Comparator MCS Unknown 30 mg —