drugset / Trial / NCT01324570

Safety, Pharmacokinetics (PK), and Efficacy of Buprenorphine Transdermal System (BTDS) in Children

NCT01324570

Phase 3 Completed 41 enrolled Purdue Pharma LP
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to characterize the safety, PK, and efficacy of BTDS in patients of ages 7 to 16 years.

Timeline

Start
2011-07
Primary completion
2016-05
Completion
2016-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Buprenorphine Other / unclassified 2.5 ug Other
Subject Buprenorphine Other / unclassified 5 ug Other
Subject Buprenorphine Other / unclassified 10 ug Other
Subject Buprenorphine Other / unclassified 20 ug Other

Indications

No indication recorded.