Clinical trial

Study to Investigate the Efficacy of a Non-hormonal Drug Against Endometriosis…

NCT00185341 · Bayer, Industry · Completed

Key facts

NCT number NCT00185341
Title Study to Investigate the Efficacy of a Non-hormonal Drug Against Endometriosis Associated Pelvic Pain
Official title A Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Evaluate the Safety, Tolerability and Efficacy of the CCR1 Antagonist ZK 811752, Given Orally in a Dose of 600 mg Three Times Daily, for the Treatment of Endometriosis Over 12 Weeks
Lead sponsor Bayer, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Endometriosis
Intervention type Drug
Interventions CCR1-Antagonist (BAY86-5047, ZK811752), Placebo
Enrollment 110
Start date Feb 1, 2005
Primary completion Feb 1, 2007
Completion Feb 1, 2007
First posted Sep 16, 2005
Last update posted May 2, 2016
Countries Czechia, Denmark, Finland, France, Netherlands, Spain, Sweden

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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