drugset / Trial / NCT00236093

Extension Study of ACTIQ Treatment for Children and Adolescents With Breakthrough Pain

NCT00236093

Phase 2 Completed Cephalon
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The objective of the study is to monitor the safety (adverse event data) of longer-term use of ACTIQ (Oral Transmucosal Fentanyl Citrate \[OTFC\]) treatment in children with pain associated with cancer, sickle cell disease, or severe burns and breakthrough pain (BTP) who are receiving around the clock (ATC) opioid therapy.

Timeline

Start
2006-10
Primary completion
2006-12
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Fentanyl Other / unclassified Oral