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High Bup Dose
High-dose buprenorphine is a partial mu-opioid receptor agonist that provides analgesia and opioid dependence treatment through sustained receptor occupancy.
High-dose buprenorphine is a partial mu-opioid receptor agonist that provides analgesia and opioid dependence treatment through sustained receptor occupancy. Used for Opioid use disorder, Chronic pain management.
At a glance
| Generic name | High Bup Dose |
|---|---|
| Also known as | Subutex |
| Sponsor | New York State Psychiatric Institute |
| Drug class | Partial mu-opioid receptor agonist |
| Target | Mu-opioid receptor (OPRM1) |
| Modality | Small molecule |
| Therapeutic area | Psychiatry / Addiction Medicine |
| Phase | Phase 3 |
Mechanism of action
Buprenorphine binds with high affinity to mu-opioid receptors in the central nervous system, producing analgesia and reducing cravings in opioid use disorder. At higher doses, it achieves greater receptor saturation and clinical efficacy while maintaining a ceiling effect on respiratory depression compared to full mu-opioid agonists. This Phase 3 trial likely evaluates optimized dosing regimens for improved treatment outcomes.
Approved indications
- Opioid use disorder
- Chronic pain management
Common side effects
- Constipation
- Nausea
- Headache
- Dizziness
- Insomnia
- Sweating
Key clinical trials
- Medication Treatment for Opioid Use Disorder in Expectant Mothers: Conceptual Model Assessments Sub-study
- Medication Treatment for Opioid Use Disorder in Expectant Mothers: Infant Neurodevelopmental Outcomes Sub-study
- Optimizing Retention, Duration and Discontinuation Strategies for Opioid Use Disorder Pharmacotherapy (RDD) (PHASE2)
- High Dose Buprenorphine (BUP) Induction in the Emergency Department (ED) (PHASE3)
- Medication Treatment for Opioid Use Disorder in Expectant Mothers (PHASE3)
- Standard Versus High Dose ED-Initiated Buprenorphine Induction (PHASE3)
- Efficacy of Computer Delivered Community Reinforcement Approach (CRA) (Bup II) (NA)
- Starting Treatment With Agonist Replacement Therapies (START) (PHASE4)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |