drugset / Trial / NCT00185341

Study to Investigate the Efficacy of a Non-hormonal Drug Against Endometriosis Associated Pelvic Pain

NCT00185341 ↗

Phase 2 Completed 110 enrolled Bayer
RandomizedParallel-groupDouble-blindTreatment

Summary

This study was designed as a proof-of-concept trial to evaluate safety, tolerability, and the efficacy of 1800 mg (ZK 811752 600 mg given orally three times daily) over 12 weeks for the treatment of endometriosis associated pelvic pain (EAPP) in comparison to placebo.

Timeline

Start
2005-02
Primary completion
2007-02
Completion
2007-02

Drugs

EvaluationDrugModalityDoseRoute
Subject BAY86-5047 Small molecule 600 mg Oral

Indications