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Vaped Marijuana to Attenuate Naloxone-Precipitated Withdrawal

Primary Purpose

Opioid Overdose

Status
Suspended
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Naloxone
Marijuana
Sponsored by
New York State Psychiatric Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Opioid Overdose

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 18-55 years of age.
  2. Diagnostic criteria for Opioid Use Disorder (OUD) moderate-severe (304.00) as per DSM-V, including physiological dependence and not currently seeking treatment for OUD.
  3. Self-reported opioid use for nontherapeutic purposes; and positive urine drug screen for opioids.
  4. Physically healthy.
  5. Normal body weight/Within 20% of body weight (for appropriate frame) according to 1983 Metropolitan Weight tables.
  6. Able to perform study procedures.
  7. Females must be either:

    1. Post-menopausal (amenorrhea for at least 12 consecutive months), surgically sterile -or
    2. Women of childbearing potential must agree to use an acceptable double-barrier method of contraception during screening and study participation.
  8. Must smoke < three cannabis cigarettes three times a week (or the vaping equivalent) for the four weeks before screening.

Exclusion Criteria:

  1. Seeking treatment for Opioid Use Disorder.
  2. Current or history of a psychiatric condition that would affect participants' ability to provide informed consent (e.g., mood disorder with functional impairment or schizophrenia) or make participant hazardous for the participant (e.g., recent suicidal ideation) or staff (e.g., significant history of violence).
  3. Current DSM-V diagnosis of substance use disorders requiring medically managed detoxification, other than OUD (e.g., alcohol or benzodiazepine dependence).
  4. Medical condition resulting in chronic pain (>3 months).
  5. Clinically significant abnormality on physical examination, vital signs, screening laboratory tests, or 12- lead ECG.
  6. Significant cardiovascular, hepatic, renal, respiratory, gastrointestinal, endocrine, immunologic, dermatologic, hematologic, or neurologic disorder.
  7. Any surgical, or medical condition that may interfere with the absorption, distribution, metabolism, or excretion of the study drugs.
  8. Baseline hypotension, orthostatic hypotension or syncope, hypertension (blood pressure > 140/90), pulmonary hypertension or heart disease.
  9. Any of the following values for laboratory tests:

    1. positive pregnancy test,
    2. hemoglobin < 12 g/dL in males and < 11 g/dL in females,
    3. neutrophil count < 1.0 × 109/L,
    4. platelet count < 75 × 109/L,
    5. creatinine clearance < 50 ml/min per modified Cockcroft-Gault equation,
    6. aspartate aminotransferase or alanine aminotransferase > 3.0 × upper limit of normal.
  10. Hypersensitivity to opioids, history of significant adverse reactions to cannabinoids, and allergy or contraindication to any other drugs administered as a part of this investigation.
  11. Use of an investigational agent within 30 days.

Sites / Locations

  • New York State Psychiatric Institute

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Experimental

Experimental

Arm Label

Naloxone 0 mg + MJ 0.0 mg

Naloxone 0 mg + MJ 12.5 mg

Naloxone 0 mg + MJ 25 mg

Naloxone 4 mg + MJ 0.0 mg

Naloxone 4 mg + MJ 12.5 mg

Naloxone 4 mg + MJ 25 mg

Arm Description

Intranasal naloxone in combination with vaped marijuana

Intranasal naloxone in combination with vaped marijuana

Intranasal naloxone in combination with vaped marijuana (MJ)

Intranasal naloxone in combination with vaped marijuana (MJ)

Intranasal naloxone in combination with vaped marijuana (MJ)

Intranasal naloxone in combination with vaped marijuana (MJ)

Outcomes

Primary Outcome Measures

Clinical Opiate Withdrawal Scale (COWS)
Clinical Opiate Withdrawal Scale is an 11-item, clinician-administered measure designed to quantify the severity of opioid withdrawal. The COWS evaluates the severity of the following symptoms on a scale of 0-4 or 5: resting pulse rate, sweating, restlessness, pupil size, bone or joint aches, runny nose or tearing, gastrointestinal upset, tremor, yawning, anxiety, or irritability, and gooseflesh. The score on the COWS ranges from 0 to 48 points with withdrawal ratings between 5-12 considered mild, 13-24 as moderate, 25-36 as moderately severe, and >36 considered severe.

Secondary Outcome Measures

Full Information

First Posted
October 5, 2021
Last Updated
August 8, 2023
Sponsor
New York State Psychiatric Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05114460
Brief Title
Vaped Marijuana to Attenuate Naloxone-Precipitated Withdrawal
Official Title
The Ability of Vaped Marijuana to Reduce the Severity of Naloxone-Precipitated Withdrawal
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Suspended
Why Stopped
The U.S. Department of Health and Human Services Office of Human Research Protections issued an FWA restriction on NYSPI research that included a pause of human subjects research as of June 23, 2023.
Study Start Date
November 1, 2021 (Actual)
Primary Completion Date
September 30, 2024 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
New York State Psychiatric Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of the proposed, proof-of-concept study is to test the combined effects of vaporized marijuana [Delta-9-tetrahydracannabinol (THC)] with NLX as a proof of concept towards the possible development of a combined overdose reversal agent with improved tolerability.
Detailed Description
The goal of the proposed, proof-of-concept study is to test the combined effects of vaporized marijuana [Delta-9-tetrahydracannabinol (THC)] with NLX as a proof of concept towards the possible development of a combined overdose reversal agent with improved tolerability. Marijuana plant material will be obtained from the National Institutes on Drug Abuse (NIDA). In clinical studies, oral synthetic THC reduced the severity of opioid withdrawal during opioid detoxification. Clinically, cannabinoid drugs like Marinol® (oral synthetic THC), Sativex ® (nabixomols), and Cesamet® (nabilone) are used to treat nausea and vomiting, common symptoms of opioid withdrawal. This study will investigate the ability of vaporized marijuana (V-MJ) (0.00, 12.5, and 25 mg: concentration= 11.7% THC + 0.04% CBD) to reduce the severity of opioid withdrawal precipitated by intranasal (IN) NLX (0.0 and 4.0 mg). This trial will recruit healthy participants with opioid use disorder (N=16, completers). Testing will begin following stabilization on oral morphine (120 mg/day), which will continue throughout the trial. During each testing session, a single V-MJ + naloxone dose combination will be assessed (in randomized order), with 48 hours between testing sessions. Laboratory testing sessions will consist of a modified naloxone challenge procedure, which quantifies the severity of naloxone-precipitated opioid withdrawal.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Overdose

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 2
Interventional Study Model
Sequential Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Naloxone 0 mg + MJ 0.0 mg
Arm Type
Placebo Comparator
Arm Description
Intranasal naloxone in combination with vaped marijuana
Arm Title
Naloxone 0 mg + MJ 12.5 mg
Arm Type
Active Comparator
Arm Description
Intranasal naloxone in combination with vaped marijuana
Arm Title
Naloxone 0 mg + MJ 25 mg
Arm Type
Active Comparator
Arm Description
Intranasal naloxone in combination with vaped marijuana (MJ)
Arm Title
Naloxone 4 mg + MJ 0.0 mg
Arm Type
Active Comparator
Arm Description
Intranasal naloxone in combination with vaped marijuana (MJ)
Arm Title
Naloxone 4 mg + MJ 12.5 mg
Arm Type
Experimental
Arm Description
Intranasal naloxone in combination with vaped marijuana (MJ)
Arm Title
Naloxone 4 mg + MJ 25 mg
Arm Type
Experimental
Arm Description
Intranasal naloxone in combination with vaped marijuana (MJ)
Intervention Type
Drug
Intervention Name(s)
Naloxone
Intervention Description
Intranasal Naloxone
Intervention Type
Drug
Intervention Name(s)
Marijuana
Intervention Description
Vaped Marijuana
Primary Outcome Measure Information:
Title
Clinical Opiate Withdrawal Scale (COWS)
Description
Clinical Opiate Withdrawal Scale is an 11-item, clinician-administered measure designed to quantify the severity of opioid withdrawal. The COWS evaluates the severity of the following symptoms on a scale of 0-4 or 5: resting pulse rate, sweating, restlessness, pupil size, bone or joint aches, runny nose or tearing, gastrointestinal upset, tremor, yawning, anxiety, or irritability, and gooseflesh. The score on the COWS ranges from 0 to 48 points with withdrawal ratings between 5-12 considered mild, 13-24 as moderate, 25-36 as moderately severe, and >36 considered severe.
Time Frame
4-weeks trial

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18-55 years of age. Diagnostic criteria for Opioid Use Disorder (OUD) moderate-severe (304.00) as per DSM-V, including physiological dependence and not currently seeking treatment for OUD. Self-reported opioid use for nontherapeutic purposes; and positive urine drug screen for opioids. Physically healthy. Normal body weight/Within 20% of body weight (for appropriate frame) according to 1983 Metropolitan Weight tables. Able to perform study procedures. Females must be either: Post-menopausal (amenorrhea for at least 12 consecutive months), surgically sterile -or Women of childbearing potential must agree to use an acceptable double-barrier method of contraception during screening and study participation. Must smoke < three cannabis cigarettes three times a week (or the vaping equivalent) for the four weeks before screening. Exclusion Criteria: Seeking treatment for Opioid Use Disorder. Current or history of a psychiatric condition that would affect participants' ability to provide informed consent (e.g., mood disorder with functional impairment or schizophrenia) or make participant hazardous for the participant (e.g., recent suicidal ideation) or staff (e.g., significant history of violence). Current DSM-V diagnosis of substance use disorders requiring medically managed detoxification, other than OUD (e.g., alcohol or benzodiazepine dependence). Medical condition resulting in chronic pain (>3 months). Clinically significant abnormality on physical examination, vital signs, screening laboratory tests, or 12- lead ECG. Significant cardiovascular, hepatic, renal, respiratory, gastrointestinal, endocrine, immunologic, dermatologic, hematologic, or neurologic disorder. Any surgical, or medical condition that may interfere with the absorption, distribution, metabolism, or excretion of the study drugs. Baseline hypotension, orthostatic hypotension or syncope, hypertension (blood pressure > 140/90), pulmonary hypertension or heart disease. Any of the following values for laboratory tests: positive pregnancy test, hemoglobin < 12 g/dL in males and < 11 g/dL in females, neutrophil count < 1.0 × 109/L, platelet count < 75 × 109/L, creatinine clearance < 50 ml/min per modified Cockcroft-Gault equation, aspartate aminotransferase or alanine aminotransferase > 3.0 × upper limit of normal. Hypersensitivity to opioids, history of significant adverse reactions to cannabinoids, and allergy or contraindication to any other drugs administered as a part of this investigation. Use of an investigational agent within 30 days.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jermaine Jones, PhD
Organizational Affiliation
New York State Psychiatric Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Vaped Marijuana to Attenuate Naloxone-Precipitated Withdrawal

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