drugset / Trial / NCT01842893

Efficacy and Safety of Fentanyl ETHYPHARM for Breakthrough Pain in Opioid-treated Patients With Cancer

NCT01842893

Phase 3 Completed 91 enrolled Ethypharm
RandomizedCrossoverTriple-blindTreatment

Summary

The purpose of the study is to assess the clinical effectiveness of Fentanyl ETHYPHARM when used to relieve breakthrough pain (BTP) in opioid-treated cancer patients.

Timeline

Start
2011-11
Primary completion
2012-07
Completion
2012-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Fentanyl Other / unclassified 133 ug Subcutaneous
Subject Fentanyl Other / unclassified 267 ug Subcutaneous
Subject Fentanyl Other / unclassified 400 ug Subcutaneous
Subject Fentanyl Other / unclassified 533 ug Subcutaneous
Subject Fentanyl Other / unclassified 800 ug Subcutaneous

Indications