Semaglutide for Helping Opioid Recovery
Purpose
The is a pilot, 12-week, double-blind, placebo-controlled, randomized trial of individuals with opioid use disorder (OUD) newly initiating buprenorphine to receive either weekly injections of semaglutide (n=23) or matching placebo (n=23). The primary aim is to determine the effects of semaglutide on cue-reactivity among individuals with OUD. The secondary aim is to assess the preliminary efficacy, safety, and tolerability of semaglutide for OUD.
Condition
- Opioid Use Disorder
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Criteria
Inclusion Criteria:
- English speaking adults aged 18 and above
- DSM-5 diagnosis of opioid use disorder, severe
- Initiated sublingual buprenorphine (SL-BUP) treatment within 60 days of enrollment
- Attained stable dosing of SL-BUP of 16mg or greater for 30 days prior to enrollment
- Anticipating continuation of SL-BUP for the duration of the trial
- Agreeable with bringing SL-BUP prescription to visits to allow study team to conduct
a dose count
- Willing to grant study team permission to communicate about SL-BUP treatment with
community prescriber via completion of 42 CFR release
Individuals with any of the following will be excluded:
- DSM-5 diagnosis of any current substance use disorder excluding opioid, cannabis or
tobacco
- Active psychosis, active suicidality or homicidality or any psychiatric condition
that impair ability to provide informed consent
- Any current or lifetime diagnosis of eating disorders
- BMI<25mg/kg2
- Current or lifetime diagnosis of Type 1 or Type 2 diabetes
- Personal or family history of medullary thyroid carcinoma or multiple endocrine
neoplasia syndrome type 2
- Use of any GLP-1 agonist medications in the prior 3 months
- Anticipating receipt of any GLP-1 agonist medications during the trial
- History of angina pectoris, coronary heart disease, congestive heart failure,
inflammatory bowel disease, chronic obstructive pulmonary disease, bariatric
surgery, idiopathic pancreatitis, diabetic gastroparesis
- Liver function test greater than 3 times upper normal limit
- Renal impairment as indicated by eGFR of <60
- History of hypersensitivity or allergy to semaglutide
- Pregnant or breastfeeding
- Anticipated to participate in a concurrent drug trial
- Any other reason or clinical condition that the investigators judge may interfere
with study participation and/or be unsafe for a participant
Study Design
- Phase
- Phase 2
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Masking Description
- The IDS will perform both the randomization and blinding, and will be the only research staff that will remain unblinded. The IDS will extract the semaglutide and draw the dose into syringes, which will be made to match visually with the placebo saline doses. All other research staff will remain blinded for the duration of the trial.
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Semaglutide |
This arm will receive semaglutide (n=23). All participants will initially receive 0.25mg for 4 weeks, and then as tolerated dose will be increased to 0.5mg for 4 weeks. Then as tolerated, the dose will be increased to 1.0mg for 4 weeks. |
|
|
Placebo Comparator Placebo |
This arm will receive saline placebo (n=23). |
|
Recruiting Locations
Boston, Massachusetts 02115
More Details
- Status
- Recruiting
- Sponsor
- Brigham and Women's Hospital
Detailed Description
Participants include N=46 men and women with DSM5 diagnosis of OUD who are newly initiating sublingual buprenorphine (SL-BUP), defined as within 60 days of enrollment. Only those participants who have attained stable SL-BUP dosing (i.e. no change in dose) for at least 30 days prior to enrollment and plan to remain on the SL-BUP for the duration of the trial will be eligible. Potential participants will be screened and enrolled only if they meet full inclusion criteria. After baseline procedures are complete, participants will be randomized to semaglutide or placebo. Following randomization, participants will be scheduled for thirteen weekly study visits. Each visit will last approximately 1 hour, except for study visits 1 (baseline), 7, and 14 (follow-up) which will take no more than 3 hours in order to conduct reward- and stress-related neurocognitive testing. At each visit, participants will complete vital signs, weight, urine toxicology testing, and a blood testing for glucose. Participants will also complete an assessment of adverse events and questionnaires probing secondary outcomes (i.e. anxiety and depression, suicidality, substance use, opioid withdrawal symptoms, craving questionnaire). Blood samples will be collected at the beginning, middle, and end of the study. At study visits 2-13, the weekly dose of semaglutide or placebo will be administered. Both participants and study staff (including raters) will be blinded to active drug vs. placebo. The medication will be purchased from the manufacturer, and stored in the BWH Investigational Drug Service (IDS). The IDS will then extract the semaglutide and draw the dose into syringes, which will be matching visually with the placebo doses.