339
Participants
Start Date
May 31, 2008
Primary Completion Date
April 30, 2011
Study Completion Date
April 30, 2011
buprenorphine/naloxone
2/0.5 mg buprenorphine/naloxone and 8/2 mg buprenorphine/naloxone sublingual tablets; dosage and frequency are subject specific; subjects will receive treatment for up to 12 months
(Multiple sites in Austria) => Coordinating CRO: H&P GmbH, Vienna
Lead Sponsor
Indivior Inc.
INDUSTRY