This is a 52-week open-label study to evaluate the safety and tolerability of ALKS 5461.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
1,485
Sublingual tablet, taken daily
Incidence of Adverse Events (AEs)
Time frame: Up to 56 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
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