Cannabis Use DisorderEarly Phase 1COBRASNCT06430580
Cannabinoids and Biological Reactivity to Stress
A Early Phase 1 study testing Hydrocortisone Oral and Yohimbine Hydrochloride in people with Cannabis Use Disorder, run by Florida State University at 1 site in United States.
Trial summary
The goal of this study is to test the impact of two drugs that produce temporary stress-like symptoms, both in isolation and together, on cannabis use motivation in individuals with Cannabis Use Disorder. The main questions it will answer are: 1. How do different forms of stress affect cannabis use motivation? 2. Read more about this study
- Who is it for?
- Ages 18 to 50 years
- Conditions the study is for
- Cannabis Use Disorder
- What is being tested?
- Hydrocortisone Oral and Yohimbine Hydrochloride
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 38 participants
- Where
- 1 siteUnited States
- Study dates
- 30 Sep 2024to 13 Aug 2026
- Phase
- Early Phase 1
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Meets criteria for current, moderate to severe Cannabis Use Disorder (CUD) as assessed by the Structured Clinical Interview (SCID) for the Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) during the screening interview.
- Reports engagement in near-daily/daily cannabis use.
- Provide a urine sample positive for THC.
- Must be in generally good health as determined by a physical exam, EKG, and blood tests
- Must be adequately informed of the nature and risks of the study and given written informed consent prior to screening.
- Able to read and write in English.
Who cannot join
- Has a history of serious psychiatric problems (i.e., psychosis, Bipolar Disorder I) or meets criteria for a current Major Depressive Episode, as assessed by the SCID-V-RV.
- Reports current suicidal ideation.
- Meets DSM-5 criteria for any other current, moderate to severe substance use disorder (other than CUD or Tobacco Use Disorder
- Has a positive result urine drug screen for all other drugs aside from THC (i.e., amphetamine, methamphetamine, benzodiazepine, cocaine, MDMA, morphine, oxycodone, methadone, buprenorphine) at screening or at any lab visit.
- Has structural brain abnormalities (e.g., neoplasms), stroke, seizures, infectious disease, a history of other neurological diseases, or a history of head trauma resulting in unconsciousness.
- Has a history of cardiovascular disease, myocardial infarction, chest pain, or palpitations on exertion or drug use, edema, hypertension, resting heart rate <50 BPM or >100 BPM. Cardiovascular diseases include:
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- . a. Benign prostatic hyperplasia (BPH) b. Post-myocardial infarction
- Demonstrates systolic BP outside of acceptable range (80-140mmHG), or diastolic BP outside of acceptable range (50-90 mmHG)
- Has a history of cor pulmonale, dyspnea, orthopnea, tachypnea (>24 breaths per minute), or uncontrolled chronic obstructive pulmonary disease or asthma.
- Currently taking any daily psychotropic medication
- Currently taking any of the following medications:
- Angiotensin-Converting Enzyme (ACE) inhibitors including Lisinopril, Enalapril, Benazepril, and Bamipril
- Angiotensin II Receptor Blockers (ARB) including Losartan, Valsartan, and Olmesartan
- Thiazide Diuretics including Hydrochlorothiazide (HCTZ), Chlorthalidone
- Calcium Channel Blockers including Amlodipine, Diltiazem, and Verapamil
- Beta-blockers including Carvedilol, Metoprolol, Atenolol, Propranolol
- Anti-Arrythmic Medication including Disopyramide, Flecainide, and Mexiletine
- Edema (Diuretics)
- Thiazide Diuretics (as above)
- Loop Diuretics including Furosemide and Torsemide
- Potassium Sparing Diuretics: Spironolactone and Eplerenone
- Anti-Platelet Medications such as Clopidogrel, Prasugrel, and Ticagrelor
- Reproductively capable candidates who are pregnant (based on urine test at screening or at any lab visit) or are heterosexually active and not using medically approved birth control measures (oral contraceptives, IUD, condom, sterilization).
- Self-reports currently seeking or engaging in CUD treatment or any other alcohol or drug treatment.
- Self-reports intent to imminently quit cannabis use.
- Has a Blood-Injection-Injury Phobia, as determined by scores greater than 15 on the Injection and Blood Draw subscale of the Medical Fear Survey
Trial locations and contacts
1 site in 1 country.
United States1 site
The BRAINS Lab at Florida State University
Tallahassee, Florida, 32306-4301
About this study
The goal of this study is to test the impact of two drugs that produce temporary stress-like symptoms, both in isolation and together, on cannabis use motivation in individuals with Cannabis Use Disorder. The main questions it will answer are:
- How do different forms of stress affect cannabis use motivation?
- How do different forms of stress affect the body's natural cannabinoids?
Read more
Researchers will compare a placebo to both drugs in isolation, as well as together, across four separate lab visits.
Participants will:
- Complete a clinical screening interview (by phone or in-person) and visit the lab for a medical screening, and if eligible:
- Visit the lab four times where they will: i). Take one of four drug combinations ii). Complete an interview, questionnaires, and computerized tasks iii). Have their brain activity recorded with an EEG cap iv). Provide three blood samples
Read the detailed description
The prevalence of daily cannabis use and cannabis use disorder (CUD) has increased in the United States over the past two decades. Unfortunately, psychosocial treatments produce minimal long-term abstinence rates and no FDA-approved medications for CUD exist. Thus, identifying novel CUD treatment targets is an increasingly urgent public health need.
Stress-elicited cannabis use motivation has been implicated in worse CUD outcomes, but a mechanistic understanding of how acute stress increases cannabis use motivation in CUD is limited. Prior work has demonstrated that acute psychosocial stress enhancement of subsequent cannabis cue incentive salience, as indexed by the late positive potential (neural measure of approach-motivated attention recorded using electroencephalography [EEG]), was associated with worse CUD severity and intervention response, independent of subjective craving. Moreover, hypothalamic pituitary adrenal [HPA]-axis, rather than noradrenergic or subjective reactivity to the psychosocial stressor was associated with subsequent potentiation of the cannabis cue-elicited late positive potential. These studies suggest that non-genomic, rapid glucocorticoid effects may be a contributing mechanism in stress amplification of neural drug-cue reactivity, but their correlational designs preclude causal inference. Further, psychosocial stressors are unable to isolate HPA-axis vs. noradrenergic components of stress reactivity.
To isolate HPA-axis activation and test causality, pharmacological manipulations, common in animal models but rare in human studies, will be used to produce separate and co-operative glucocorticoid (20mg hydrocortisone) and noradrenergic (54mg yohimbine) activation. The investigators will employ a 2x2 randomized, placebo-controlled double-blind crossover design in 36 participants with severe CUD. The primary aim is to test the causal potentiating effect of glucocorticoids on drug-cue reactivity and drug use motivation, and further determine if the effect depends on co-occurring noradrenergic stimulation. Preclinical work indicates that glucocorticoids can potentiate reward motivation via mobilization of endocannabinoid activity (primary target of cannabis). Thus, as an exploratory aim, the investigators will obtain plasma samples to test the impact of pharmacological stress on circulating endocannabinoids (2-AG, AEA) and their mediating role in glucocorticoid potentiation of drug-cue reactivity and drug use motivation. This project represents a highly novel integration of a rigorous pharmacological challenge design with biological markers of drug-cue incentive salience and endocannabinoid system activity. If hypotheses are confirmed, one causal mechanism through which stress increases neural cannabis cue reactivity will be known, which has immediate implications for testing experimental therapeutics. The long-term goal is to understand how a stress-related mechanism predictive of worse CUD phenotype is generated and can be blocked in CUD. Development of this model will provide a valid, efficient and (relative to other neuroimaging methods) low-cost approach to screen candidate medications and optimize psychosocial drug cue exposure therapies.
- Conditions
- Cannabis Use Disorder
- Being tested
- Hydrocortisone Oral, Yohimbine Hydrochloride, Cornstarch Placebo 20mg, Cornstarch Placebo 54mg
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Hydrocortisone OralDrug
20mg hydrocortisone, single oral dose
Yohimbine HydrochlorideDrug
54mg yohimbine hcl, single oral dose
Cornstarch Placebo 20mgDrug
20mg cornstarch placebo, single oral dose
Cornstarch Placebo 54mgDrug
54mg cornstarch placebo, single oral dose
| Study group | Role | What they receive |
|---|---|---|
| 20mg hydrocortisone + 54mg yohimbine hcl | Experimental | 20mg hydrocortisone, single oral dose 54mg yohimbine hcl, single oral dose Receives: Drug: Hydrocortisone Oral; Drug: Yohimbine Hydrochloride |
| 20mg hydrocortisone + 54mg placebo | Experimental | 20mg hydrocortisone, single oral dose 54mg cornstarch placebo, single oral dose Receives: Drug: Hydrocortisone Oral; Drug: Cornstarch Placebo 54mg |
| 20mg placebo + 54mg yohimbine hcl | Active comparator | 20mg cornstarch placebo, single oral dose 54mg yohimbine hcl, single oral dose Receives: Drug: Yohimbine Hydrochloride; Drug: Cornstarch Placebo 20mg |
| 20mg placebo + 54mg placebo | Placebo comparator | 20mg cornstarch placebo, single oral dose 54mg cornstarch placebo, single oral dose Receives: Drug: Cornstarch Placebo 20mg; Drug: Cornstarch Placebo 54mg |
What is being measured
The primary outcome is the main question the study is designed to answer.
Amplitude of neurophysiological response to cannabis cues (μV)
Change in electroencephalography-recorded (EEG) late positive potential amplitude to cannabis cue images after hydrocortisone (with or without yohimbine) compared to placebo+placebo and yohimbine+placebo conditions (higher amplitudes indicate worse outcome)
Measured: Late positive potential amplitude outcome is assessed at each of the four lab visits, which take place over the study period (10-22 days)
Amplitude of Demand Intensity for Cannabis (# of hits at $0)
Marijuana purchase task-derived Intensity after hydrocortisone administration (with or without yohimbine) compared to placebo+placebo and yohimbine+placebo (increased Intensity indicates worse outcome)
Measured: Intensity is assessed at each of the four lab visits, which take place over the study period (10-22 days)
Peak Total Monetary Expenditure for Cannabis (total amount of money spent on hits)
Marijuana purchase task-derived OMax after hydrocortisone administration (with or without yohimbine) compared to placebo+placebo and yohimbine+placebo (increased OMax indicates worse outcome)
Measured: OMax is assessed at each of the four lab visits, which take place over the study period (10-22 days)
Breakpoint of Monetary Expenditure for Cannabis (price at which no hits are purchased)
Marijuana purchase task-derived Breakpoint after hydrocortisone administration (with or without yohimbine) compared to placebo+placebo and yohimbine+placebo (increased Breakpoint indicates worse outcome)
Measured: Breakpoint is assessed at each of the four lab visits, which take place over the study period (10-22 days)
Sensitivity of Cannabis Hit Purchasing Behavior to Price Increases
Marijuana purchase task-derived Elasticity after hydrocortisone administration (with or without yohimbine) compared to placebo+placebo and yohimbine+placebo (decreased Elasticity indicates worse outcome)
Measured: Elasticity is assessed at each of the four lab visits, which take place over the study period (10-22 days)
Frequency of implicit cannabis image choice
Change in cannabis image selections on the Implicit Image Choice Task (computerized behavioral task; range 0-30; higher scores indicate worse outcome) after hydrocortisone administration (with and without yohimbine) compared to placebo+placebo and yohimbine+placebo
Measured: Implicit choice task # of cannabis image selections outcome is assessed at each of the four lab visits, which take place over the study period (10-22 days)
Frequency of explicit cannabis image choice
Change in cannabis image selections on the Explicit Image Choice Task (computerized behavioral task; range 0-30; higher scores indicate worse outcome) after hydrocortisone administration (with and without yohimbine) compared to placebo+placebo and yohimbine+placebo
Measured: Explicit choice task # of cannabis image selections outcome is assessed at each of the four lab visits, which take place over the study period (10-22 days)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 May 2024
- Study start30 Sep 2024
- Primary completion13 Aug 2026
- Study completion13 Aug 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cannabis Use DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Early Phase 1
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- 2x2 randomized double-blind within-subject crossover
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 38 participants (actual)
Sponsor and investigators
- Lead sponsor
- Florida State University
- Sponsor type
- University, hospital or other
- Collaborators
- Wayne State University, National Institute on Drug Abuse (NIDA), Auburn University
- Responsible party
- Principal investigator, Rick James Macatee, Florida State University
- Investigators
- Richard J Macatee, PhD, Principal investigator, Florida State University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06430580
- Sponsor's protocol ID
- STUDY00006376
- Other IDs
- R21DA058780-01A1
- Acronym
- COBRAS
- Status last verified
- Sep 2026
- First submitted
- 13 May 2024
- Last updated
- 22 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No