drugset / Trial / NCT00318500

Study Evaluating the Safety and Efficacy of ERB-041 on Reduction of Symptoms Associated With Endometriosis in Reproductive-Aged Women

NCT00318500 ↗

Phase 2 Completed 150 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to evaluate the efficacy and safety of two doses of ERB-041 (75 mg and 150 mg) relative to placebo on the relief of endometriosis-related symptoms (dysmenorrhea, pelvic pain, and deep dyspareunia) in reproductive aged women.

Timeline

Start
2006-05
Primary completion
—
Completion
2006-12

Drugs

EvaluationDrugModalityDoseRoute
Subject PRINABEREL Small molecule 75 mg —
Subject PRINABEREL Small molecule 150 mg —