drugset / Trial / NCT00486811

A Study to Evaluate the Efficacy and Safety of CG5503 Prolonged Release (PR) in Subjects With Moderate to Severe Chronic Pain Due to Osteoarthritis of the Knee

NCT00486811

RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate whether tapentadol (CG5503) prolonged-release (PR) tablets at doses of 100-250 mg twice daily provide a better pain relief in patients with moderate to severe chronic pain due to osteoarthritis of the knee than a placebo (a medication without active substance). In addition the tolerability of CG5503 PR will be assessed. One third of the patients will receive CG5503 and one third will receive placebo. For further comparison one third of the patients will receive oxycodone controlled release (CR) at doses of 20-50 mg twice daily which is an active approved pain medication. Please note that tapentadol ER (Extended Release) and tapentadol PR (Prolonged Release) are identical and used interchangeably. This is due to United States of America and European naming conventions.

Timeline

Start
2007-06
Primary completion
2008-07
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Oxycodone Other / unclassified 20 mg
Comparator Oxycodone Other / unclassified 30 mg
Comparator Oxycodone Other / unclassified 40 mg
Comparator Oxycodone Other / unclassified 50 mg
Subject Tapentadol Small molecule 100 mg Oral
Subject Tapentadol Small molecule 150 mg Oral
Subject Tapentadol Small molecule 200 mg Oral
Subject Tapentadol Small molecule 250 mg Oral

Indications