The manufacturer of SUBLOCADE® will discontinue supply in Australia on 31 December 2026.
This is a commercial decision and not related to safety or efficacy.
ODT prescribers should work with patients to plan their next steps early to support continuity of treatment. Check the dedicated NSW Health webpage for updates.
Based on the most recent evidence, this guidance supersedes all existing guidance on transitioning from Sublocade to other opioid dependence treatment formulations, including the NSW Health Guidance Long-Acting Injectable Buprenorphine for Opioid Dependence Treatment.
Figure 1: Pharmacokinetic parameters at buprenorphine (BPN) steady state equilibrium comparing Subutex, Sublocade and Buvidal Cmin Cavg and Cmax
This chart compares steady-state buprenorphine concentrations (ng/mL) across four formulations: Subutex, Sublocade, Buvidal Weekly and Buvidal Monthly. Each bar shows the approximate range of concentrations achieved at different dose strengths.
For Subutex, concentrations increase with dose, ranging from approximately 0.66 to 4.27 ng/mL at 8 mg, 0.87 to 5.6 ng/mL at 12 mg, 1.04 to 6.77 ng/mL at 16 mg, 1.37 to 8.86 ng/mL at 24 mg, and 1.98 to 15.63 ng/mL at 32 mg.
For Sublocade, concentrations range from approximately 2.46 to 5.1 ng/mL at 100 mg and 5.47 to 11.81 ng/mL at 300 mg.
For Buvidal Weekly, concentrations increase from approximately 0.89 to 1.7 ng/mL at 8 mg, 0.84 to 4.30 ng/mL at 16 mg, 1.20 to 5.00 ng/mL at 24 mg, and 2.63 to 6.87 ng/mL at 32 mg.
For Buvidal Monthly, concentrations increase from approximately 0.92 to 3.8 ng/mL at 64 mg, 1.4 to 5.9 ng/mL at 96 mg, 2.09 to 11.1 ng/mL at 128 mg, and 2.66 to 15.4 ng/mL at 160 mg.
Note: In Figure 1, Buvidal is represented as a mix of modelled data from Camurus data on file [15] (8 mg and 24 mg Weekly doses and 64 mg and 96 mg Monthly doses) and measured data presented in the European Public Assessment Report for Buvidal [16] (16 mg and 32 mg Weekly doses and 128 mg and 160 mg Monthly doses). All figures presented are geometric means.