Overview
Efficacy and Safety of SH T00660AA in Treatment of Endometriosis
Status:
Completed
Completed
Trial end date:
2006-09-01
2006-09-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this study is to demonstrate safety and efficacy of SH T00660AA compared to placebo in the treatment of endometriosisPhase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Bayer
Criteria
Inclusion Criteria:- Female patients with endometriosis-associated pelvic pain
Exclusion Criteria:
- Pregnant or lactating women
- history or suspicion of hormone dependent tumor
- therapy resistant endometriosis
- need for primary surgical treatment
- any other conditions which forbid the participation.