Post-marketing commitment to the European Medicines Agency to conduct a prospective, controlled study of the transfer from Subutex to Suboxone.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
241
Suboxone sublingual tablet 4 mg/1 mg - 24 mg/6 mg, daily for 28 days
Subutex sublingual tablet 4-24 mg, daily for 28 days
Response Rate
Response rate was defined as the percentage of participants who did not receive a dose increase from the dose given at the first dosing date by Day 7 of a one-week, randomized, double-blind, double-dummy treatment transfer phase.
Time frame: Assessed by Day 7 of double-blind, double-dummy treatment period.
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