81
Participants
Start Date
February 28, 2013
Primary Completion Date
August 9, 2013
Study Completion Date
August 9, 2013
Placebo
Placebo solution + Placebo ALO-02 (intact)
intact ALO-02 60 mg/7.2 mg
Placebo solution + ALO-02 60 mg/7.2 mg (intact)
crushed ALO-02 60 mg/7.2 mg
crushed ALO-02 60 mg/7.2 mg in solution + placebo ALO-02 (intact)
crushed oxycodone IR 60 mg
crushed oxycodone immediate-release (IR) 60 mg in solution + placebo ALO-02 (intact)
crushed ALO-02 40 mg/4.8 mg
crushed ALO-02 40 mg/4.8 mg in solution + placebo ALO-02 (intact)
crushed oxycodone IR 40 mg
crushed oxycodone immediate-release (IR) 40 mg in solution + placebo ALO-02 (intact)
INC Research Toronto, Inc., Toronto
Lead Sponsor
Collaborators (1)
Syneos Health
OTHER
Pfizer
INDUSTRY