drugset / Trial / NCT01151098

Safety of Buprenorphine Transdermal Systems in Subjects With Chronic Nonmalignant Pain - a 28-week Extension Study

NCT01151098

Phase 3 Completed 189 enrolled Purdue Pharma LP
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study was to evaluate the long-term safety and tolerability of 7-day BTDS in a 28-week open-label extension phase in subjects with chronic nonmalignant pain syndromes whose pain had been previously controlled by oral opioid combination therapy.

Timeline

Start
2001-04
Primary completion
2002-02
Completion
2002-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Buprenorphine Other / unclassified 5 ug Other
Subject Buprenorphine Other / unclassified 10 ug Other
Subject Buprenorphine Other / unclassified 20 ug Other

Indications