Open Label Comparison of Injectable Buprenorphine ( Brixadi®) and Naltrexone (Vivitrol®) for Opioid Use Disorder

Opioid Use Disorder Clinical Trial

Official title:

Open Label Comparison of Injectable Buprenorphine ( Brixadi®) and Naltrexone (Vivitrol®) for Opioid Use Disorder

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05596955
• Other study ID #: 843403
• Status: Recruiting
• Phase: Phase 2
• Start date: January 12, 2023
• Est. completion date: July 2028

Study information

• Verified date: February 2024
• Source: University of Pennsylvania
• Contact: Urooj Iqbal
• Phone: 215-746-7281
• Email: Urooj.Iqbal[@]pennmedicine.upenn.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This project aims to elucidate the brain effects of opioid use disorder (OUD) treatments. The study will investigate the cognitive effects of extended-release preparations of a partial opioid agonist and an antagonist. To this end, the study will use up to three monthly injections of buprenorphine (XRBUP, Brixadi®) and naltrexone (XRNTX, Vivitrol®). Domain-specific brain activity will be induced by cognitive tasks and recorded with Magnetic Resonance Imaging. Participants will be imaged at baseline and in the interval between the 1st and 2nd injection and followed for up to three months.

Description:

This study will elucidate the cognitive mechanisms of response to opioid agonists and antagonists used to prevent relapse in OUD through investigation of the underlying neural circuits. The study will use previously validated cognitive probes, functional Magnetic Resonance Imaging (fMRI), and extended-release injectable preparations of opioid partial agonist buprenorphine (XRBUP, Brixadi) and opioid antagonist naltrexone (XRNTX, Vivitrol), in OUD patients. Using two medications with opposing mu opioid receptor action, the study will allow a comprehensive evaluation of the mechanisms of response to relapse prevention pharmacotherapy in OUD. The study will determine the presence of treatment effects in the domains of executive function, incentive salience, and resting functional connectivity and the interaction that will indicate a difference between the two medications. The study will evaluate the ability of the brain fMRI signal to explain relapse defined by % of opioid-positive urine tests and adherence to the study interventions. The study will screen recently detoxified treatment-seeking participants with OUD who will receive 2 monthly injections of XR-NTX or XR-BUP and have weekly urine toxicology monitoring. The project will enroll 200 participants over 6 years. The proposal would be the first neural systems' level investigation of the cognitive effects of the next generation extended release preparation of buprenorphine and naltrexone to explain the individual heterogeneity of OUD treatment response and failure. This project has the potential to advance the theory and personalized treatment of OUD by elucidating the brain mechanisms of vulnerability to relapse in OUD and in SUD in general.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: July 2028
• Est. primary completion date: July 2028
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria

1. 18-65 Years old

2. OUD by DSM5 Criteria, confirmed by history and physical examination including urine toxicology, medical records and self-report

3. Opioids are the drug of choice

4. Interested in either injectable extended release agonist or antagonist treatment

5. Have a stable address, working command of English language, and telephone access.

Exclusion Criteria

1. Lifetime diagnoses of any psychotic disorder, e.g. schizophrenia, schizoaffective disorder and bipolar affective disorder type 1.

2. Psychiatric disorders requiring current medication treatment, e.g. moderate to severe depression, with the exception of mild to moderate Depressive and Anxiety disorders and Attention Deficit Hyperactivity Disorder that does not require prescription stimulants.

3. Polysubstance users whose drug of choice is not an opioid.

4. Medical contraindications for the study medications, e.g. active liver disease.

5. Medical and surgical conditions such as malignancy that may affect patients' ability to receive XRNTX or XRBUP treatment because it may interfere with opioid analgesia.

6. Contraindications for MRI, e.g. claustrophobia, indwelling foreign magnetic agents.

7. Women of childbearing age who do not use an effective contraceptive.

Related Conditions & MeSH terms

• Opioid Use Disorder
• Opioid-Related Disorders
• Substance-Related Disorders

Intervention

Drug:
• Buprenorphine injection
Extended release once-a-month buprenorphine injection . Study arm undergoes 2 fMRI examinations and weekly monitoring visits
• Naltrexone Injection
Extended release once-a-month naltrexone injection. Study arm undergoes 2 fMRI examinations and weekly monitoring visits

Locations

Country	Name	City	State
United States	Addiction Treatment Center, University of Pennsylvania	Philadelphia	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Fronto-limbic brain fMRI response to XRNTX and XRBUP		Phase 1 (Years 1-2)
Primary	Fronto-limbic brain fMRI response to XRNTX and XRBUP		Phase 2 (Years 3-6)
Primary	Urine Toxicology	Percentage of urine tests positive for opioids	Phase 1 (Years 1-2)
Primary	Urine Toxicology	Percentage of urine tests positive for opioids	Phase 2 (Years 3-6)
Secondary	Self-reported continued opioid use	Report of illicit opioid use measured by Timeline Follow-Back Interview (TLFB)	Phase 1 (Years 1-2)
Secondary	Self-reported continued opioid use	Report of illicit opioid use measured by Timeline Follow-Back Interview (TLFB)	Phase 2 (Years 3-6)
Secondary	Adherence to treatment	The proportion of missed follow up visits out of the total available	Phase 1 (Years 1-2)
Secondary	Adherence to treatment	The proportion of missed follow up visits out of the total available	Phase 2 (Years 3-6)
Secondary	Opioid Craving	Self-reported craving for opioids measured standard clinical questionnaire (OCS) to determine opioid craving severity (0-10). Higher rating on items indicate more severe craving symptoms and increased likelihood of near term use.	Phase 1 (Years 1-2)
Secondary	Opioid Craving	Self-reported craving for opioids measured standard clinical questionnaire (OCS) to determine opioid craving severity (0-10). Higher rating on items indicate more severe craving symptoms and increased likelihood of near term use.	Phase 2 (Years 3-6)
Secondary	Self-reported Opioid Withdrawal	Measured by items using a Likert scale (0-4), Subjective Opioid Withdrawal Scale (SOWS), with higher ratings indicating more severe symptoms of opioid withdrawal	Phase 2 (Years 3-6)
Secondary	Clinician-reported Opioid Withdrawal	Measured by clinician-assessed values for Clinician Administered Opioid Withdrawal Scale (COWS) scale items. Higher values indicate more severe symptoms of opioid withdrawal.	Phase 2 (Years 3-6)