drugset / Trial / NCT00712595

Mifepristone for Treatment of Uterine Fibroids

NCT00712595

Phase 2/3 Completed 200 enrolled Mediterranea Medica S. L.
RandomizedParallel-groupDouble-blindTreatment

Summary

The objectives of this study are to estimate the efficacy and safety of the daily administration of mifepristone 5 mg versus 10 mg for three months for the treatment of uterine fibroids. The hypothesis of the study is that both mifepristone doses reduce the volume of the myoma in about 40% after 3 months of treatment.

Timeline

Start
2007-01
Primary completion
2007-01
Completion
2009-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Mifepristone Small molecule 5 mg Oral
Subject Mifepristone Small molecule 10 mg Oral

Indications