This is a Phase 3 study designed to evaluate the safety and tolerability of two titration schedules for ALKS 5461.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
66
Sublingual tablet taken once daily
Alkermes Investigational Site
Jacksonville, Florida, United States
Alkermes Investigational Site
Orlando, Florida, United States
Alkermes Investigational Site
Atlanta, Georgia, United States
Alkermes Investigational Site
Number of Subjects With Adverse Events (AEs)
Time frame: 8 weeks
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Saint Charles, Missouri, United States
Alkermes Investigational Site
Staten Island, New York, United States
Alkermes Investigational Site
Dayton, Ohio, United States
Alkermes Investigational Site
Allentown, Pennsylvania, United States
Alkermes Investigational Site
Bellevue, Washington, United States
Alkermes Investigational Site
Halifax, Nova Scotia, Canada