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Taking people in United StatesPhase 2

Cannabidiol and Cannabis Concentrate Users

Key facts

Who runs it
University of Colorado, Denver
Where
Aurora, United StatesSee the site
Trial code
Status
Recruiting
Phase
Phase 2
People taking part
120 people, planned
Started
4 Dec 2024
Expected to end
30 Jun 2028
Type of study
Interventional, 3 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • Broad Spectrum Cannabidiol (bsCBD) 400 mg
  • Broad Spectrum Cannabidiol (bsCBD) 200 mg
  • Placebo
Record updated
1 May 2026

Who can take part

Age
25 years to 60 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 20 criteriaShow less

Who can take part

  • Age 25-60
  • Regular use (at least 4 times per week) of cannabis concentrates for the last year
  • Not currently seeking to cut down or stop cannabis use
  • At least one episode of 3 consecutive days of cannabis abstinence with no experience of severe withdrawal symptoms (i.e., >=4 DSM-5 Cannabis Withdrawal symptoms rated as "severe"), in the last 90 days
  • At least two symptoms of a DSM-5 cannabis use disorder

Who cannot take part

  • Current use of any psychotropic (e.g., antidepressants, anxiogenics) or hepatotoxic medications
  • Current use of strong or moderate CYP3A4 inhibitors or inducers (commonly used examples not captured by other exclusion criteria include protease inhibitors, macrolide antibiotics [e.g., erythromycin], azole antifungals [e.g., ketoconazole], verapamil, and grapefruit juice)
  • Current use of strong or moderate CYP2C19 inhibitors or inducers (commonly used examples not captured by other exclusion criteria include proton pump inhibitors, prednisone, and norethisterone)
  • For female patients of childbearing potential, not willing to use at least an approved method of birth control while taking the study medication, unless she is surgically sterile, partner is surgically sterile or she is postmenopausal (one year)
  • Meets DSM-5 diagnostic criteria for a psychotic disorder (e.g., schizophrenia, schizophreniform disorder, schizoaffective disorder), bipolar disorder, or major depression with suicidal ideation, or has a history of treatment for these disorders
  • Current cardiovascular or respiratory disease (e.g., coronary artery disease, severe asthma, chronic obstructive pulmonary disease, etc.)
  • Currently use of anti-epileptic medications (e.g., clobazam, sodium valproate) or medications known to have major interactions with Epidiolex (buprenorphine, leflunomide, levomethadyl acetate, lomitapide, mipomersen, pexidartinib, propoxyphene, sodium oxybate, and/or teriflunomide) or a history of seizures
  • Current or past hepatocellular disease, as indicated by medical history or alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2 times the upper limit of the normal range at screening
  • Use of any illicit substance besides alcohol, nicotine, or cannabis (e.g., cocaine, opiates, methamphetamine, MDMA, benzodiazepines, or barbiturates) in the past 60 days, as indicated by self-report and urine toxicology screening at the beginning of each study visit
  • Use of CBD-containing products other than cannabis concentrates in the past 90 days
  • Alcohol use on 3 or more days per week, and/or > 3 drinks per drinking day in the past 60 days. Participants must also have a breath alcohol level of 0 at the beginning of each study visit
  • Daily nicotine use
  • For female participants, pregnancy or trying to become pregnant. A positive pregnancy test at the beginning of any study visit will result in exclusion from ongoing study participation
  • For female participants, currently lactating
  • Current suicidality risk as indicated during the conduct of the C-SSRS with concurrence after a study physician's or PI evaluation if the response to C-SSRS questions 1 or 2 is "yes"

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 25 and 60 years old?

Where in United States

  • University of Colorado Anschutz Medical CampusAurora, United StatesContact: Joseph P Schacht, PhDTaking people

About the trial

What the trial wants to find out

This study is a randomized, placebo-controlled, dose-ranging trial of plant-derived cannabidiol (CBD) among people who regularly use cannabis concentrates but are not trying to stop or cut down on their use. The main questions it aims to answer are whether CBD, relative to placebo, reduces cannabis concentrate use, the subjective effects of cannabis, or cannabis craving. Participants will take CBD (200 mg or 400 mg per day) or placebo for 4 weeks and will complete three visits during the study medication period, all conducted using a mobile laboratory.

The 3 groups in the trial

  • Broad Spectrum Cannabidiol (bsCBD) 400 mgExisting treatment, for comparison

    bsCBD in a 400 mg dose will be used as described in the study arms.

  • Broad Spectrum Cannabidiol (bsCBD) 200 mgExisting treatment, for comparison

    bsCBD in a 200 mg dose will be used as described in the study arms.

  • PlaceboPlacebo, for comparison

    A medically inert placebo medication will be used as described in the study arms.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Cannabidiol and Cannabis Concentrate Users: A Randomized, Placebo Controlled Study
Fit questions
Built from NCT06575751, who can take part
Record updated
1 May 2026