drugset / Trial / NCT00160459

A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment of Uterine Fibroids

NCT00160459

Phase 2 Completed 129 enrolled Abbott
RandomizedParallel-groupTriple-blindTreatment

Summary

This study was designed to determine the safety and effectiveness of 3 asoprisnil doses compared to placebo, taken for 12 weeks by women with uterine fibroids.

Timeline

Start
2000-05
Primary completion
2001-07
Completion
2001-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Asoprisnil Other / unclassified 5 mg Oral
Subject Asoprisnil Other / unclassified 10 mg Oral
Subject Asoprisnil Other / unclassified 25 mg Oral

Indications