Pregabalin Plus Lofexidine for the Outpatient Treatment of Opioid Withdrawal
Purpose
A placebo-controlled trial in which male and female outpatients with an opioid use disorder who express interest in extended-release injectable naltrexone (XR-NTX) are randomized 1:1 to lofexidine/pregabalin or lofexidine/pregabalin placebo for withdrawal management and offered XR-NTX if after completing withdrawal.
Conditions
- Opiate Withdrawal Syndrome
- Opioid Use
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- Male and/or female subjects ≥ 18 years of age 2. Meet DSM-5 criteria for an Opioid Use Disorder with physiologic features. Have met 2 or more of the 11 criteria for an OUD including tolerance and withdrawal within the last 12 months 3. Interested in opioid antagonist treatment 4. Used opioids in 20 or more of the last 30 days 5. A stable address in the local area; not planning to move in the next 60 days. 6. Have documents for ID check 7. Absence of medical or psychiatric conditions that are likely to interfere with study participation 8. Has 12 lead ECG demonstrating a QTc ≤450 msec and a QRS ≤120 msec. Site PI has final determination for study inclusion if readings exceed these limits. The PENN cardiologists and medical monitor are available for consultation when needed 9. Negative pregnancy test and using adequate contraception if of childbearing potential.
Exclusion Criteria
- Current psychotic disorder (bipolar I, schizophrenia, major depression that is not in remission 2. Alcohol, benzodiazepine, or other sedative use disorder with physiological features that require medication for detoxification 3. Allergy or other serious adverse event due to treatment with pregabalin, XR-NTX, or lofexidine 4. Pending incarceration or plans to leave the immediate area in the next 30 days 5. Homicidal or otherwise behaviorally disturbed requiring immediate attention 6. High risk for suicide as determined by answering 'yes' to questions 4 and/or 5 on C-SSRS 7. Blood pressure <90 mm Hg (systolic) or <60 mm Hg (diastolic). If value out of normal range, the investigator and study Clinician will decide subject inclusion/exclusion on case-by-case basis 8. Heart rate and/or pulse<50 bpm at screening-sitting 9. An Estimated Glomerular Filtration Rate eGFR<70 mL/min/1.73m2 10. A History of, or current Seizure disorder (excluding childhood febrile seizures) 11. Inability to read and/or understand English. For example, unable to understand the informed consent as demonstrated by failing to answer 9/10 questions correctly on the quiz 12. 12. Pregnant or breastfeeding 13. 13. Currently taking sympathomimetic drugs, or a thiazolidinedione antidiabetic 14. ALT and/or AST >4X upper limit of normal 15. A Child-Pugh score >7 16. Currently receiving opioids for pain management 17. In a treatment study where medication was administered in the last 30 days 18. Currently using medications that are known to be strong or moderate inhibitors of CYP2D6 such as fluoxetine, paroxetine, mirabegron, bupropion, quinidine, terbinafine, cimetidine, cinacalcet, duloxetine, or fluvoxamine 19. In a methadone maintenance or buprenorphine treatment program within the last 30 days
Study Design
- Phase
- Phase 2
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Intervention Model Description
- Active pregabalin plus lofexidine versus placebo pregabalin plus lofexidine
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Investigator)
- Masking Description
- double-blind placebo-controlled randomized trial
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental LFX/PGB |
PGB/day 1=400mg, day 2-7=600mg each day, day 8=400mg, day 9=200mg, day 10=100mg LFX/day 1=1.62mg, day 2-7=2.16mg each day, day 8=1.44mg, day 9=0.72mg, day 10=0.72mg |
|
|
Active Comparator LFX/PLA-PGB |
PLA-PGB/day 1-7= 0mg each day, day 8, 9, and 10 =0mg each day LFX/ day 1=1.62mg, day 2-7=2.16mg each day, day 8=1.44mg, day 9=0.72mg, day 10=0.72mg |
|
Recruiting Locations
Philadelphia, Pennsylvania 19104
More Details
- NCT ID
- NCT05995535
- Status
- Recruiting
- Sponsor
- University of Pennsylvania
Detailed Description
A placebo-controlled trial in which male and female outpatients with an opioid use disorder who express interest in extended-release injectable naltrexone (XR-NTX) are randomized 1:1 to lofexidine/pregabalin or lofexidine/pregabalin placebo for withdrawal management and offered XR-NTX if after completing withdrawal. It follows a UG3 study in which 90 inpatients with an OUD who expressed interest in XR-NTX were randomized 2:1 to withdrawal management with lofexidine/pregabalin or lofexidine/placebo pregabalin. Results were that the conditions were equally safe, and that lofexidine/pregabalin was more effective in reducing subjective withdrawal and keeping patients in treatment than lofexidine/placebo pregabalin. The objectives are to study the safety and effectiveness of lofexidine/pregabalin compared to lofexidine/placebo for managing opioid withdrawal and transitioning to XR-NTX in outpatient settings.