Induction of Opioid-Dependent Individuals Onto Buprenorphine and Buprenorphine/Naloxone
Completed
Indivior Inc.
Phase 2
2008-03-01
The purpose of this study is to compare the presence, degree, time course and profile of
opioid withdrawal symptoms associated with induction onto new formulations of buprenorphine
or buprenorphine/naloxone in persons with active opioid dependence. The primary outcome
measure is the severity of withdrawal symptoms measured using the Clinical Opiate Withdrawal
Scale (COWS). The primary study hypothesis is that neither drug formulation will precipitate
an opioid withdrawal syndrome.
Buprenorphine Formulation Comparison: Sublingual Tablet vs. Solution - 1
Completed
National Institute on Drug Abuse (NIDA)
Phase 1/Phase 2
1997-10-01
The purpose of this study is to compare subject response to liquid vs. tablet formulations,
to assess bioequivalency of liquid vs. tablet, to compare subject preference, and to evaluate
if dose response curve for tablet is equal to liquid form."
Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules - 1
Completed
University of California, Los Angeles
Phase 3
2003-06-01
The purpose of this protocol is to to compare the clinical utility of two dosage tapering
regimens in Buprenorphine/Naloxone stabilized subjects for opiate detoxification.
Bridging Active Heroin Users to Hepatitis C Treatment Using Buprenorphine - 1
Completed
Organization to Achieve Solutions in Substance Abuse (OASIS)
N/A
2003-06-01
The purpose of this study is to see whether street-recruited heroin users can be successfully
treated for hepatitis C after stabilizing them on buprenorphine.
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