Clinical trial

Understanding the Clinical Pharmacology of Marijuana-Tobacco Co-administration

Name
23-38884
Description
This is a crossover, randomized, double-blinded clinical pharmacology study enrolling dual cannabis-tobacco smokers to better understand the combined effects of co-administering cannabis and tobacco. The project aims to describe the pharmacokinetics and pharmacodynamics of marijuana-tobacco co-administration by delivering THC and nicotine in various combinations. This foundational study will establish a research program focused on elucidating the public health consequences of marijuana-tobacco co-use.
Trial arms
Trial start
2023-10-31
Estimated PCD
2028-10-31
Trial end
2028-10-31
Status
Not yet recruiting
Phase
Early phase I
Treatment
Cannabis
Participants will vape marijuana in varying doses from the PAX device
Arms:
High marijuana and Very Low Nicotine Content cigarette, High marijuana and regular cigarette, High marijuana only, Medium marijuana and Very Low Nicotine Content cigarette, Medium marijuana and regular cigarette, Placebo marijuana and Very Low Nicotine Content cigarette, Placebo marijuana and regular cigarette
Nicotine
Participants will vape regular and Very Low Nicotine content cigarettes from the PAX device
Arms:
High marijuana and Very Low Nicotine Content cigarette, High marijuana and regular cigarette, Medium marijuana and Very Low Nicotine Content cigarette, Medium marijuana and regular cigarette, Placebo marijuana and Very Low Nicotine Content cigarette, Placebo marijuana and regular cigarette, Regular cigarette only
Pax Loose Leaf Vaporizer
In all arms, participants will be using the PAX Loose Leave Vaporizer.
Arms:
High marijuana and Very Low Nicotine Content cigarette, High marijuana and regular cigarette, High marijuana only, Medium marijuana and Very Low Nicotine Content cigarette, Medium marijuana and regular cigarette, Placebo marijuana and Very Low Nicotine Content cigarette, Placebo marijuana and regular cigarette, Regular cigarette only
Size
48
Primary endpoint
Change in peak plasma concentration of THC
Baseline and Day 1
Change in peak plasma concentration of THC
Day 1 and Day 2
Change in peak plasma concentration of THC
Day 2 and Day 3
Change in peak plasma concentration of THC
Day 3 and Day 4
Change in peak plasma concentration of THC
Day 4 and Day 5
Change in peak plasma concentration of THC
Day 5 and Day 6
Change in peak plasma concentration of THC
Day 6 and Day 7
Change in peak plasma concentration of THC
Day 7 and Day 8
Change in Peak plasma concentration of nicotine
Baseline and Day 1
Change in Peak plasma concentration of nicotine
Day 1 and Day 2
Change in Peak plasma concentration of nicotine
Day 2 and Day 3
Change in Peak plasma concentration of nicotine
Day 3 and Day 4
Change in Peak plasma concentration of nicotine
Day 4 and Day 5
Change in Peak plasma concentration of nicotine
Day 5 and Day 6
Change in Peak plasma concentration of nicotine
Day 6 and Day 7
Change in Peak plasma concentration of nicotine
Day 7 and Day 8
Eligibility criteria
Inclusion Criteria: * Heart rate \< 105 BPM\* * Systolic Blood Pressure \< 160 and \> 90\* * Diastolic Blood Pressure \< 100 and \> 50\* \*Considered out of range if both machine and manual readings are above/below these thresholds. * Body Mass Index ≤ 38.0 (at investigator's discretion for higher BMI if no other concurrent health issues) * Current regular user of cannabis who smokes or vapes cannabis or THC extracts at least three days a week for the past 3 months or more * Test positive for D-9-tetrahydrocannabinol (THC) at screening and self-report of cannabis use * Current user of inhaled forms of tobacco/nicotine (cigarette, cigars, e-cigarettes) who use the product daily for the past 3 months or more * Saliva cotinine ≥ 30 ng/mL Exclusion Criteria: * Unstable medical conditions: * Heart disease * Seizures * Cancer * Thyroid disease (okay if controlled with medication) * Diabetes * Hepatitis B or C or Liver disease * Glaucoma * Kidney disease or urinary retention * An ulcer in the past year * Active use of an inhaler for asthma or COPD * Hypertension if uncontrolled (meaning participant has a diagnosis, but they are not taking medication/under treatment (e.g., diet or exercise plan) * Drug/Alcohol Dependence * Alcohol or illicit drug dependence within the past 12 months (currently in treatment) with the exception of those who recently completed an alcohol/drug treatment program * Positive toxicology test at the screening visit (THC \& prescribed medications okay) * Opioid replacement therapy (including methadone, buprenorphine, or other) * Psychiatric conditions * Current or past schizophrenia, and/or current or past bipolar disorder * Major depression, current or within the past year * Major personality disorder * Participants with current or past minor or moderate depression and/or anxiety disorders will be reviewed by the PI \[study physician\] and considered for inclusion * History of psychiatric hospitalizations are not exclusionary, but study participation will be determined as per PI's \[study physician's\] approval * Current regular use of any psychiatric medications with the exception of SSRIs and SNRIs and current evaluation by the PI that the participant is otherwise healthy, stable, and able to participate * Congenital or acquired immunodeficiency disorders (i.e. HIV, congenital immune deficiency syndrome, chronic diseases) * Other disorders (i.e. ICU, malnutrition, immunosuppressive therapy) * Traumatic brain injury * Recent onset or change (worsening) in cough, fever and/or abdominal symptoms (vomiting or pain) in the past two weeks * Medications * Use of medications that are inducers of nicotine metabolizing enzyme CYP2A6 (Example: rifampicin, dexamethasone, phenobarbital, and other anticonvulsant drugs) * Concurrent use of nicotine-containing medications * Any stimulant medications (ex. Adderall) generally given for ADHD treatment * Other/Misc. Chronic Health Problems * Oral thrush * Fainting * Other "life threatening illnesses" as per study physician's discretion * Pregnancy * Pregnancy (self-reported and urine pregnancy test) * Breastfeeding (determined by self-report) * Concurrent participation in another clinical trial * Inability to communicate in English * History of marijuana-induced psychosis or paranoia after smoking marijuana * Scoring a 7 or higher on the Severity of Dependence Scale (SDS) for cannabis use * Planning to quit smoking or vaping within the next 60 days * Planning to quit cannabis use within the next 60 days * Uncomfortable with getting blood drawn * Willingness to abstain from tobacco smoking and all combustible products for 13 hours before admission * Willingness to abstain from smoking/ingestion of cannabis 13 hours before * Willingness to abstain from nicotine products 13 hours before each admission
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'CROSSOVER', 'primaryPurpose': 'BASIC_SCIENCE', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 48, 'type': 'ESTIMATED'}}
Updated at
2023-08-21

1 organization

2 products

6 indications

Product
Cannabis
Indication
cannabis
Indication
Cannabis Use
Indication
Tobacco Use
Indication
Vaping
Product
Nicotine