Oral Cannabidiol for Opioid Withdrawal

Johns Hopkins University3 enrolled

Overview

This pilot study will examine the safety of the cannabinoid cannabidiol (Epidiolex) in a human laboratory model of clinically relevant withdrawal. The study will be a residential within-subject comparison; all participants will receive placebo dosing and active cannabidiol. Results may be used to support an R01 grant application to more closely examine this hypothesis.

Based on preclinical research and emerging human research, cannabidiol (CBD; a major constituent of the cannabis plant) is a promising pharmacotherapy for the treatment of opioid withdrawal. Most recently, CBD decreased cue-induced craving and anxiety (two common withdrawal symptoms) among abstinent heroin-dependent individuals relative to placebo. As of June 2018, Epidiolex, an oral formulation of plant-derived pure CBD, has been approved by the U.S. Food and Drug Administration (FDA) for treating severe forms of epilepsy and can be prescribed for other off-label indications. Epidiolex has a low side effect and high safety profile. Given the recent FDA approval of Epidiolex, and a growing interest to develop existing pharmaceuticals to address issues related to Opioid Use Disorder (OUD) and its recovery, the investigators are proposing a pilot study to examine the safety of Epidiolex in a human laboratory model of clinically relevant withdrawal. The study will be a residential within-subject comparison; methadone-maintained participants will undergo spontaneous withdrawal and receive placebo dosing and active cannabidiol. Data collected for this study will establish: (1) the safety of administering two dosing regimens of Epidiolex within the investigators' withdrawal paradigm and (2) the feasibility of the investigators' withdrawal paradigm for demonstrating clinically meaningful increases in withdrawal. Results may be used to support an R01 grant application to more closely examine this hypothesis.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Opioid Withdrawal Opioid Craving Opioid Use Disorder

Interventions

EpidiolexDRUG

Epidiolex 100 mg/mL Oral Solution

PlaceboDRUG

Cherry syrup oral solution

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Medically cleared to take study medication * Are not pregnant or breast feeding * Willing to comply with the study protocol * Provides urine that tests positive for methadone * Maintained on 80-120 mg of daily methadone with no dose changes in the past 2 weeks (verified through a medical release with the participant's provider) Exclusion Criteria: * Meet Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria for alcohol/substance use disorder other than opioid use disorder * Previous adverse reaction to a cannabinoid product * Self-report any illicit drug use or cannabinoid use in the past 7 days * Presence of any clinically significant medical/psychiatric illness judged by the investigators to put subject at elevated risk for experiencing an adverse events * Past year suicidal behavior as assessed via the Columbia Suicide Severity Rating Scale * History of seizure disorder * Past 14 day use of any of the following contraindicated medications: * Clobazam, Valproate * Moderate or strong inhibitors of CYP3A4 or CYPC19 (with the exception of methadone, as outlined in the Protection Against CBD Risks section). * Strong CYP3A4 or CYP2C19 inducers * UGT1A9, UGT2B7, CYP1A2, CYP2C8, CYP2C9 and CYP2C19 substrates (with the exclusion of caffeine). * Central nervous system (CNS) depressants that are contraindicated with Epidiolex * Breathalyzer that tests positive for alcohol prior to session admission * Self-reported consumption of grapefruit juice within 24 hours of session admission * Have a history of clinically significant cardiac arrhythmias or vasospastic disease * Have circumstances that the study investigators believe are contraindicated with study participation and/or would interfere with study participation (e.g., impending jail). * Moderate-severe hepatic impairment as indicated by ALT or AST levels \> 3x ULN and/or Bilirubin levels \>2x ULN as evidenced by a blood test.

Locations (1)

Johns Hopkins University

Baltimore, Maryland, United States

Outcomes

Primary Outcomes

Safety as Assessed by Number of Adverse Events

Number of Adverse Events reported across sessions with and without study drug. Adverse events were collected for the entire 57 hour session.

Time frame: through completion of the two study sessions, an average of 17 days

Number of Participants Whose Aspartate Aminotransferase (AST)/Alanine Aminotransferase (ALT) Levels >3x Upper Limit of Normal

Number of participants whose AST/ALT levels \>3x upper limit of normal (ULN) at the end of a study session when they receive Epidiolex and Placebo. This will be used in the assessment of safety.

Time frame: End of residential stay, prior to discharge

Change in Withdrawal Scores From Baseline AfterReceiving Placebo

Change in withdrawal scores during laboratory evaluation of spontaneous withdrawal. Withdrawal is measured with the Subjective Opiate Withdrawal Scale (SOWS). That has a range of 0-64 where a mild score is represented by a score of 1-10, a moderate score is represented by a score of 11-20 and a severe score is considered anything greater than 21.

Time frame: Baseline, during residential session up to 57 hours

Secondary Outcomes

Initial Efficacy of Study Drug as Assessed by Area Under the Curve for the Subjective Opiate Withdrawal Scale (SOWS) Scores

Withdrawal symptom suppression during active and placebo conditions. Area Under the Curve (AUC) analyses will be calculated to characterize withdrawal on the Subjective Opiate Withdrawal Scale (SOWS) scores across time. SOWS AUC will be compared between the two conditions. AUC will range from 0 to 3072 where 0 represents no withdrawal during study drug administration and 3072 represents the most severe withdrawal during study drug administration.

Time frame: After first administration of study drug and up to 48 hours

Acceptability Assessed by Number of Participants Who Would Recommend the Medication to a Family Member or Friend

Data from ClinicalTrials.gov

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