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Active Not Recruiting
NCT06441604
Extended-release Buprenorphine as a Novel Low-dose Induction Strategy
Conditions: Opioid Use Disorder
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE2
Enrollment: 8
Sponsor: Brigham and Women's Hospital
Location: Brigham and Women's Hospital Boston Massachusetts
Summary
This is a clinical trial to characterize the safety and pharmacokinetics of using extended-release buprenorphine (XR-BUP) as a novel low-dose buprenorphine induction strategy. Individuals with a diagnosis of Opioid Use Disorder (OUD) (n=30) will be admitted to an inpatient unit to complete study procedures over the course of 3 days. Participants will receive fentanyl to prevent the emergence of withdrawal. Each participant will then receive a single injection of XR-BUP after which study staff will monitor for any precipitated withdrawal.
Eligibility Criteria
Inclusion Criteria:
* English speaking adults aged 18 and above.
* diagnosis of opioid use disorder.
* Self-reporting use of illicit opioids in \>21 days in the prior 30 days.
* Provide urine toxicology testing positive for fentanyl at baseline.
Exclusion Criteria:
* Seeking medication treatment for opioid use disorder with sublingual buprenorphine or methadone.
* Received buprenorphine or methadone treatment in prior 30 days.
* Current diagnosis of alcohol or sedative/hypnotic use disorder.
* Positive urine drug screen for benzodiazepines, alcohol and or methadone.
* Physical dependence on alcohol or sedative/hypnotics.
* Psychotic disorder, active suicidality or homicidally or any psychiatric condition that impair ability to provide informed consent.
* Have a history or diagnosis of Intracranial mass/bleed, seizure disorder, liver cirrhosis, renal failure, obstructive lung disease, hyperthyroidism, narrow-angle glaucoma, valvular heart disease, cardiac arrhythmias, heart failure.
* Recent (within 6 months) head trauma, stroke, or myocardial infarction
* Requiring treatment with opioids for acute or chronic pain.
* History of hypersensitivity or allergy to buprenorphine or fentanyl.
* Pregnant or breastfeeding.
* Liver function test greater than 3 times upper normal limit.
* Receiving medications that are strong or moderate CYP34A inducers or inhibitors (including but not limited to ketoconazole, itraconazole, clarithromycin, fluconazole, erythromycin), in the past 30 days.
Source: ClinicalTrials.gov (NCT06441604). StuddyBuddy aggregates publicly available trial information.