drugset / Trial / NCT00237536

Study of the Efficacy and Safety of Lonidamine for the Treatment of Symptomatic Benign Prostatic Hyperplasia

NCT00237536 ↗

Phase 2 Terminated 240 enrolled Threshold Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this trial is to evaluate the dose response relationship of lonidamine and the primary efficacy endpoint, International Prostate Symptom Score (IPSS), in subjects with symptomatic benign prostatic hyperplasia (BPH).

Timeline

Start
2005-06
Primary completion
2006-08
Completion
2006-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Lonidamine Small molecule — —