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RecruitingPhase 3

Efficacy of PP-01 in Mitigating Cannabis Withdrawal Symptoms in Adults With Cannabis Use Disorder

PleoPharma, Inc. · with National Institute on Drug Abuse (NIDA) · NCT07644052

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Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–55 · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 3
Target enrollment
420
US sites recruiting
22
Study start
June 17, 2026
Record last updated
September 28, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This study is a randomized, double-blind, placebo and active-controlled, multicenter trial conducted to evaluate whether PP-01 mitigates the withdrawal symptoms associated with discontinuing cannabis in participants with moderate to severe cannabis use disorder (CUD). Study participants will receive PP-01, nabilone, or placebo every day for 34 days. The total study duration will be approximately 78 days, including screening and a one-week inpatient stay. Following the initial inpatient portion of the study, participants will return to the clinic for six clinic visits and complete two telemedicine appointments. Participants will complete daily symptom diaries and other study-related questionnaires.

Participants who complete the core study may be eligible to participate in a repeat dosing extension study if they meet required criteria.

Being studied: PP-01; Nabilone; Placebo

Conditions: Cannabis Withdrawal

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Generally healthy adults between the ages of 18 and 55, inclusive.
  • Meet DSM-5 diagnostic criteria for current moderate to severe CUD as confirmed by a licensed physician or psychologist or addiction medicine specialist.
  • BMI within 18.0 to 38.0 kg/m2, inclusive.
  • Female participants must not be pregnant or lactating. If of childbearing potential - the participant agrees to use an accepted contraceptive regimen.
  • Male participants who are fertile and engage in sexual activity must agree to use a double barrier method (e.g., condom and spermicide) during the study and to not donate sperm for 90 days after the last dose of study medication.
  • Be seeking and motivated to discontinue cannabis and to minimize withdrawal symptoms.
  • Agree to not use cannabis or any product containing CBD, hemp derivatives, terpenes or any THC containing product including delta-8, delta-10, THC-A or any other cannabinoid-like product following Randomization and throughout the study duration.
  • Meet DSM-5 Cannabis Withdrawal Criteria.
  • Report heavy use of daily/near daily cannabis.
  • Have a urine drug screen positive for THC/THC metabolite and have a negative result for all other illicit/excluded drugs and alcohol at Screening and Randomization.
  • Capable of giving informed consent and stated willingness to comply with all study procedures including inpatient and weekly outpatient visits, daily evening video calls, restrictions, and availability for the duration of the study.
  • Willing to be admitted to an inpatient clinic with overnight stays on Days 1 through 6 and return for all outpatient visits.
  • Ability to take study drug capsules at approximately the same time each day.
  • Have regular access to the internet and access to video/virtual capabilities for video calls by any means.
  • Agree to not use any alcohol during the study.
  • No plan to change current nicotine use.
  • Ability to read, understand, and complete daily diaries.

Exclusion Criteria

  • Lifetime history of DSM-5 diagnosis of schizophrenia, schizoaffective disorder, or bipolar disorder.
  • Current DSM-5 criteria for a psychiatric disorder that in the Investigator's judgment is unstable, would be disrupted by the study medication, or is likely to require new pharmacotherapy or psychotherapy during the study period. Individuals who are currently stable on psychotropic medication for at least 3 months may be included at the discretion of the Investigator's judgement.
  • Participants who meet DSM-5 criteria for any history of or current drug use disorder within the previous 2 years, other than cannabis, nicotine, or caffeine use disorders.
  • Participants who consume alcohol on a regular or frequent basis and who do not agree or are deemed by the Investigator to be unable to discontinue alcohol for the duration of the study.
  • Participants using cannabis for a physician directed medical condition requiring use such as epilepsy.
  • Any clinically important abnormalities on Screening physical examination, assessments, electrocardiogram, or laboratory tests.
  • Current or recent history of significant violent or suicidal behavior, risk for suicide or homicide.
  • History of clinically significant medical condition that, in the opinion of the Principal Investigator, would jeopardize the safety of the participant or impact on the validity of the study results.
  • Participants with risk factors for seizure.
  • Known history of allergy, intolerance, or hypersensitivity to nabilone, gabapentin, or pregabalin.
  • Prohibited medications at Screening:
  • Current use of narcotics, psychedelics, stimulants, opioid agonists and antagonists, kratom, illicit drugs, ketamine, unregulated psychoactive drugs (sometimes known as "gas station drugs"), or products intended to induce a feeling of being high except for cannabis
  • Regular benzodiazepine use (more than once per week) and no use within 7 days of Baseline Visit (Day 1)
  • Current use (within 7 days of Baseline Visit) of OTC products to help with sleep or anxiety
  • Prescription medications to help with sleep or anxiety within 14 days of Screening
  • Current use of nabilone, dronabinol, Sativex, Epidiolex, synthetic cannabinoids
  • Gabapentin or pregabalin or use within 30 days of Screening
  • Heavy users of alcohol within 60 days of Screening or binge drinkers of alcohol within 30 days of Screening.
  • A positive urine drug/alcohol test at Screening or Randomization for narcotics and/or illicit drugs other than cannabis. If the test is positive for benzodiazepines or alcohol at Screening, and if it is reported that they are only occasional users, a repeat urine drug screen can be performed at the discretion of the Medical Monitor and must be negative at the time of Randomization.
  • Use of an investigational drug or biologic within 30 days or 5 times the half-life (whichever is longer) prior to the Screening Visit.
  • Active influenza or COVID-19 infection or planned vaccination.
  • Prior participation in any PleoPharma clinical study.

Recruiting US locations

  • Woodland International Research Group, LLC

    Little Rock, AR 72211

    Site contact: George Konis, MD

  • Woodland Research Northwest, LLC

    Rogers, AR 72758

    Site contact: Ryan Mahelona, MD

  • Yale Stress Center

    New Haven, CT 06519

    Site contact: Rajita Sinha, PhD

  • University Clinical Research-DeLand, LLC d/b/a Accel Research Sites - DeLand Clinical Research Unit

    DeLand, FL 32720

    Site contact: Bruce G. Rankin, DO

  • Research Centers of America

    Hollywood, FL 33024

    Site contact: Edwin A. Gomez, MD

  • Sandhill Research, LLC d/b/a Accel Research Sites - St. Pete - Largo Clinical Research Unit

    Largo, FL 33777

    Site contact: Rosario B. Hidalgo, MD

  • ForCare Clinical Research

    Tampa, FL 33613

    Site contact: Marlene P. Hart, MD

  • Neuroscience Research Institute

    West Palm Beach, FL 33407

    Site contact: Danesh Alam, MD

  • Sandhill Research, LLC d/b/a Accel Research Sites - NeuroStudies Clinical Research Unit 755

    Decatur, GA 30030

    Site contact: Marshall L. Nash, MD, FAHA, CPI, FAPCR

  • Evergreen Clinical Trials

    Norcross, GA 30092

    Site contact: Dmitriy Pelishev, DO

  • CenExel iResearch, LLC

    Savannah, GA 31405

    Site contact: Nancy E. Backus, MD

  • AMR Clinical

    Lexington, KY 40509

    Site contact: Peter Akpunonu, MD

  • Maryland Psychiatric Research Center, University of Maryland School of Medicine

    Baltimore, MD 21228

    Site contact: David A Gorelick, MD, PhD

  • Oasis Clinical Research

    Las Vegas, NV 89121

    Site contact: Stephen Tam, MD

  • Hassman Research Institute, LLC d/b/a CenExel Marlton, NJ

    Marlton, NJ 08053

    Site contact: Elan A. Cohen, PhD

  • The Research Foundation for Mental Hygiene/ New York State Psychiatric Institute

    New York, NY 10032

    Site contact: John Mariani, MD

  • Richmond Behavioral Associates

    Staten Island, NY 10314

    Site contact: Romana Kulikova, MD

  • Neuro-Behavioral Clinical Research, Inc.

    North Canton, OH 44720

    Site contact: Shishuka Malhotra, MD

  • Coastal Carolina Research Center, LLC

    North Charleston, SC 29405

    Site contact: Elizabeth Perkins, MD

  • AMR Clinical

    Knoxville, TN 37920

    Site contact: Jerry L. Punch, MD

  • Community Clinical Research, Inc.

    Austin, TX 78754

    Site contact: David Brown, MD

  • Memorial Hermann Village

    Houston, TX 77043

    Site contact: Dominick Stevan D'Aunno, MD

Study contacts (from the official record)

  • LBR Regulatory · 859-426-5035 · lois.rosenberger@lbria.com
  • PleoPharma, Inc. · 610-937-2882 · jcon@pleopharma.com
Efficacy of PP-01 in Mitigating Cannabis Withdrawal Symptoms in… (NCT07644052) | Bored Studies