A Study to Characterize the Abuse Liability of ALO-02 in Healthy, Non-Dependent, Recreational Opioid Abusers

PHASE1CompletedINTERVENTIONAL
Enrollment

81

Participants

Timeline

Start Date

February 28, 2013

Primary Completion Date

August 9, 2013

Study Completion Date

August 9, 2013

Conditions
Healthy
Interventions
DRUG

Placebo

Placebo solution + Placebo ALO-02 (intact)

DRUG

intact ALO-02 60 mg/7.2 mg

Placebo solution + ALO-02 60 mg/7.2 mg (intact)

DRUG

crushed ALO-02 60 mg/7.2 mg

crushed ALO-02 60 mg/7.2 mg in solution + placebo ALO-02 (intact)

DRUG

crushed oxycodone IR 60 mg

crushed oxycodone immediate-release (IR) 60 mg in solution + placebo ALO-02 (intact)

DRUG

crushed ALO-02 40 mg/4.8 mg

crushed ALO-02 40 mg/4.8 mg in solution + placebo ALO-02 (intact)

DRUG

crushed oxycodone IR 40 mg

crushed oxycodone immediate-release (IR) 40 mg in solution + placebo ALO-02 (intact)

Trial Locations (1)

M5V 2T3

INC Research Toronto, Inc., Toronto

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Syneos Health

OTHER

lead

Pfizer

INDUSTRY

NCT01746901 - A Study to Characterize the Abuse Liability of ALO-02 in Healthy, Non-Dependent, Recreational Opioid Abusers | Biotech Hunter | Biotech Hunter