What are the treatment outcomes of Brixadi (buprenorphine) versus Sublocade (buprenorphine) for opioid use disorder?

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Last updated: October 25, 2025View editorial policy

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Comparison of Brixadi vs Sublocade Treatment Outcomes for Opioid Use Disorder

Both Brixadi (buprenorphine) and Sublocade (buprenorphine) are effective long-acting injectable formulations for opioid use disorder treatment, with Sublocade having more established clinical evidence showing 61.5-75.8% abstinence rates after 12 months of treatment and retention rates of approximately 50%. 1

Overview of Long-Acting Injectable Buprenorphine Options

  • Long-acting injectable buprenorphine formulations represent an advancement in medication-assisted treatment for opioid use disorder (OUD), offering alternatives to daily oral or sublingual administration 2
  • Both Brixadi (CAM 2038) and Sublocade (RBP-6000) are subcutaneous buprenorphine depot formulations specifically developed for OUD treatment 2
  • These formulations are recommended for patients who have been stabilized on transmucosal buprenorphine and can help address adherence challenges associated with daily dosing 3

Clinical Efficacy of Sublocade

  • Sublocade demonstrated strong clinical outcomes in a 12-month study with 61.5% of continuing participants and 75.8% of new participants achieving abstinence after a full year of treatment 1
  • Retention rates for Sublocade treatment were approximately 50.6% for participants continuing from previous studies and 50.5% for new participants after 12 months 1
  • The standard protocol for Sublocade involves initial doses of 300 mg monthly for the first two months, followed by maintenance doses of 100 mg monthly 3
  • Sublocade has been shown to reduce opioid cravings and block the euphoric effects of opioids, similar to other buprenorphine formulations 4

Clinical Considerations for Both Formulations

  • Patients must be stabilized on 8-24 mg daily of sublingual or buccal buprenorphine for at least 7 consecutive days before transitioning to any injectable formulation to avoid precipitated withdrawal 3
  • Both formulations require patients to demonstrate tolerance to buprenorphine before initiation 3
  • Monitoring for injection site reactions is important, though these are typically mild to moderate in severity 1
  • The incidence of treatment-emergent adverse events with Sublocade decreases over time, with fewer events reported in the second 6 months of treatment compared to the first 6 months 1

Dosing Considerations

  • Higher buprenorphine dosing (up to 32 mg/day in oral formulations) has been associated with improved outcomes, including decreased opioid use and better retention rates 5
  • This suggests that adequate dosing of long-acting formulations is similarly important for optimal treatment outcomes 5
  • For Sublocade, the recommended maintenance dose is 100 mg monthly, though some patients may benefit from continuing the 300 mg monthly dose 3

Integration with Comprehensive Treatment

  • All medication-assisted treatments for OUD, including long-acting buprenorphine formulations, are most effective when combined with behavioral therapies 6
  • Evidence-based treatment for OUD typically includes medication-assisted treatment with buprenorphine or methadone in combination with behavioral therapies 6
  • Integrated treatment approaches that address substance use disorders alongside HIV prevention and treatment (when applicable) show improved outcomes 6

Provider Requirements and System Considerations

  • Providers must have appropriate training and certification to prescribe buprenorphine products for OUD 6
  • Barriers to buprenorphine treatment include lack of institutional support, insufficient mental health and psychosocial support resources, time constraints, and lack of specialty backup 6
  • Expanding access to medication-assisted treatment is a priority, as many patients with OUD do not receive appropriate medical treatment 4

While both Brixadi and Sublocade offer advantages over daily buprenorphine administration, Sublocade currently has more robust long-term efficacy data demonstrating sustained abstinence and reasonable retention rates in OUD treatment.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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