A Bioavailability and Safety Study of Probuphine Versus Sublingual Buprenorphine in Patients With Opioid Dependence

PHASE3TerminatedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

September 30, 2008

Primary Completion Date

December 31, 2008

Study Completion Date

December 31, 2008

Conditions
Opioid Dependence
Interventions
DRUG

Probuphine (buprenorphine implant)

Implantable formulation of buprenorphine made of buprenorphine HCl/ethylene vinyl acetate, considered a drug. (4 implants)

DRUG

Sublingual Buprenorphine

16 mg/day, QD

Trial Locations (1)

33308

Segal Institute For Clinical Research, Fort Lauderdale

Sponsors
All Listed Sponsors
lead

Titan Pharmaceuticals

INDUSTRY

NCT00768482 - A Bioavailability and Safety Study of Probuphine Versus Sublingual Buprenorphine in Patients With Opioid Dependence | Biotech Hunter | Biotech Hunter