drugset / Trial / NCT01259102

Examine Plasma Concentrations of Buprenorphine Following Reapplication of Buprenorphine Transdermal System (BTDS) After Variable Application Site Rest Periods

NCT01259102 ↗

Phase 1 Completed 70 enrolled Purdue Pharma LP
Non-randomizedParallel-groupOpen-label

Summary

The purpose of this study is to determine the pharmacokinetics of BTDS following same-site patch reapplication after rest intervals.

Timeline

Start
2000-11
Primary completion
2001-03
Completion
2001-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Buprenorphine transdermal patch Unknown 10 ug Other

Indications

No indication recorded.