Recruiting
Phase 3

PP-01

Sponsor:

PleoPharma, Inc.

Code:

NCT07644052

Conditions

Cannabis Withdrawal

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Not accepted

Interventions

PP-01

Nabilone

Placebo

Study Details

Brief summary:

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.

Conditions

Cannabis Withdrawal

Study ID

NCT07644052

Start date

Jun 17, 2026

Status verified date

Sep, 2026

Completion date

Sep, 2027

Anticipated

Primary completion date

Jun, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 55

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Generally healthy adults between the ages of 18 and 55, inclusive.
2. Meet DSM-5 diagnostic criteria for current moderate to severe CUD as confirmed by a licensed physician or psychologist or addiction medicine specialist.
3. BMI within 18.0 to 38.0 kg/m2, inclusive.
4. Female participants must not be pregnant or lactating. If of childbearing potential - the participant agrees to use an accepted contraceptive regimen.
5. 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.
6. Be seeking and motivated to discontinue cannabis and to minimize withdrawal symptoms.
7. 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.
8. Meet DSM-5 Cannabis Withdrawal Criteria.
9. Report heavy use of daily/near daily cannabis.
10. 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.
11. 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.
12. Willing to be admitted to an inpatient clinic with overnight stays on Days 1 through 6 and return for all outpatient visits.
13. Ability to take study drug capsules at approximately the same time each day.
14. Have regular access to the internet and access to video/virtual capabilities for video calls by any means.
15. Agree to not use any alcohol during the study.
16. No plan to change current nicotine use.
17. Ability to read, understand, and complete daily diaries.

Exclusion Criteria:

1. Lifetime history of DSM-5 diagnosis of schizophrenia, schizoaffective disorder, or bipolar disorder.
2. 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.
3. 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.
4. 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.
5. Participants using cannabis for a physician directed medical condition requiring use such as epilepsy.
6. Any clinically important abnormalities on Screening physical examination, assessments, electrocardiogram, or laboratory tests.
7. Current or recent history of significant violent or suicidal behavior, risk for suicide or homicide.
8. 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.
9. Participants with risk factors for seizure.
10. Known history of allergy, intolerance, or hypersensitivity to nabilone, gabapentin, or pregabalin.
11. 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
12. Heavy users of alcohol within 60 days of Screening or binge drinkers of alcohol within 30 days of Screening.
13. 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.
14. Use of an investigational drug or biologic within 30 days or 5 times the half-life (whichever is longer) prior to the Screening Visit.
15. Active influenza or COVID-19 infection or planned vaccination.
16. Prior participation in any PleoPharma clinical study.

Study Design

Enrollment

420 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: PP-01

Oral PP-01 tapered/titrated over 34 days

active comparator: Nabilone

Oral Nabilone tapered/titrated over 34 days

placebo comparator: Placebo

Oral Placebo given daily for 34 days

Interventions

PP-01

Cannabinoid-1 (CB1) partial agonist / GABAergic modulator

Nabilone

CB1 partial agonist

Placebo

Placebo comparator

Primary outcome measure

  • AUCs of the CSCW over Days 2 to 7, inclusive, comparing PP-01 vs Placebo [ Time Frame: Days to 2 to 7 ]
  • AUCs of the CSCW over Days 25 to 35, inclusive, comparing PP-01 vs Nabilone to assess rebound [ Time Frame: Days 25 to 35 ]

Central Contacts and Locations

Locations

Woodland International Research Group, LLC

Recruiting

Little Rock, Arkansas, United States, 72211

Principal Investigator:

George Konis, MD

Woodland Research Northwest, LLC

Recruiting

Rogers, Arkansas, United States, 72758

Principal Investigator:

Ryan Mahelona, MD

Yale Stress Center

Recruiting

New Haven, Connecticut, United States, 06519

Principal Investigator:

Rajita Sinha, PhD

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

Recruiting

DeLand, Florida, United States, 32720

Principal Investigator:

Bruce G. Rankin, DO

Research Centers of America

Recruiting

Hollywood, Florida, United States, 33024

Principal Investigator:

Edwin A. Gomez, MD

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

Recruiting

Largo, Florida, United States, 33777

Principal Investigator:

Rosario B. Hidalgo, MD

ForCare Clinical Research

Recruiting

Tampa, Florida, United States, 33613

Principal Investigator:

Marlene P. Hart, MD

Neuroscience Research Institute

Recruiting

West Palm Beach, Florida, United States, 33407

Principal Investigator:

Danesh Alam, MD

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

Recruiting

Decatur, Georgia, United States, 30030

Principal Investigator:

Marshall L. Nash, MD, FAHA, CPI, FAPCR

Evergreen Clinical Trials

Recruiting

Norcross, Georgia, United States, 30092

Principal Investigator:

Dmitriy Pelishev, DO

CenExel iResearch, LLC

Recruiting

Savannah, Georgia, United States, 31405

Principal Investigator:

Nancy E. Backus, MD

AMR Clinical

Recruiting

Lexington, Kentucky, United States, 40509

Principal Investigator:

Peter Akpunonu, MD

Maryland Psychiatric Research Center, University of Maryland School of Medicine

Recruiting

Baltimore, Maryland, United States, 21228

Principal Investigator:

David A Gorelick, MD, PhD

Oasis Clinical Research

Recruiting

Las Vegas, Nevada, United States, 89121

Principal Investigator:

Stephen Tam, MD

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

Recruiting

Marlton, New Jersey, United States, 08053

Principal Investigator:

Elan A. Cohen, PhD

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

Recruiting

New York, New York, United States, 10032

Principal Investigator:

John Mariani, MD

Richmond Behavioral Associates

Recruiting

Staten Island, New York, United States, 10314

Principal Investigator:

Romana Kulikova, MD

Neuro-Behavioral Clinical Research, Inc.

Recruiting

North Canton, Ohio, United States, 44720

Principal Investigator:

Shishuka Malhotra, MD

Coastal Carolina Research Center, LLC

Recruiting

North Charleston, South Carolina, United States, 29405

Principal Investigator:

Elizabeth Perkins, MD

AMR Clinical

Recruiting

Knoxville, Tennessee, United States, 37920

Principal Investigator:

Jerry L. Punch, MD

Community Clinical Research, Inc.

Recruiting

Austin, Texas, United States, 78754

Principal Investigator:

David Brown, MD

Memorial Hermann Village

Recruiting

Houston, Texas, United States, 77043

Principal Investigator:

Dominick Stevan D'Aunno, MD

More Information

Sponsor

PleoPharma, Inc.

Last update posted

Sep 2, 2026

Last verified

Sep, 2026

Keywords

  • Cannabis Use Disorder
  • Marijuana Use Disorder

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by PleoPharma, Inc. on 2026-09-02.