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The Pharmacokinetics of Single Dose Oral Tetrahydrocannabinol and Cannabidiol

The Pharmacokinetics of Oral Tetrahydrocannabinol and Cannabidiol Across the Spectrum of Glomerular Filtration Rate: a PharmacoKinetic Study

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05742724
Acronym
POT-GFR-PK
Enrollment
24
Registered
2023-02-24
Start date
2024-01-11
Completion date
2025-03-01
Last updated
2024-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis, Chronic Kidney Diseases, Dialysis

Keywords

Pharmacokinetics

Brief summary

POT-GFR-PK is a single dose pharmacokinetic study oral tetrahydrocannabinol (THC) and cannabidiol (CBD) in healthy adult controls and individuals with chronic kidney disease including those treated with in-center hemodialysis.

Detailed description

Adults aged greater than 25 years including 6 with eGFR\>60ml/min/1.73m2, 6 eGFR 30-59ml/min/1.73m2, 6 eGFR \<30ml/min/1.73m2 (CKD Epidemiology Collaboration equation) and 6 receiving in-center hemodialysis at least 2x weekly via a tunnelled catheter will receive THC 0.1mg/kg and CBD 2mg/kg by mouth in the form of MediPharm Labs-001 (MPL-001) (50mg CBD/2mg THC per 1mL). In healthy controls and participants with chronic kidney disease, blood samples will be collected at t=0, 1, 2, 3, 3.5 and 4 hours post THC/CBD administration. In participants receiving in-center hemodialysis, blood samples will be collected at t=0, 1, 2, 3, 3.5 and 4 hours post THC/CBD administration and during hemodialysis at t=0, 60, 120, 180 minutes and 15 minutes prior to the end of hemodialysis (at a reduced pump speed with blood flow 50-100ml/min) and 60 minutes post-hemodialysis. A 24 hour urine will be collected in all participants except those receiving hemodialysis without any residual urine output. Dialysate samples will be collected at 1,2,3 hours during hemodialysis and at the end of hemodialysis. Blood samples will also be collected at 24 and 48 hours. Plasma, urine and dialysis cannabinoids (THC, CBD and their metabolites) will be quantified using Multisegment Injection-Capillary Electrophoresis-Mass Spectrometry.

Interventions

DRUGTetrahydrocannabinol-Cannabidiol Combination

Oral THC 0.1mg/kg and CBD 2.5mg/kg

Sponsors

Center for Medicinal Cannabis Research
CollaboratorOTHER
McMaster University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. adult age\>25 years 2. estimated glomerular filtration rate (eGFR)\>60ml/min/1.73m2 or eGFR\<60ml/min/1.73m2 by the CKD Epidemiology Collaboration equation including in-center hemodialysis at least 2x weekly for a minimum of 3 hours per treatment via a tunnelled catheter treated \>90 days 3. agree to take the medication as directed in the study 4. provides informed consent

Exclusion criteria

1. body mass index \<20 or \>35kg/m2 2. physical dependence on any drug other than caffeine or nicotine 3. history of clinically significant adverse event associated with cannabis intoxication 4. history of psychosis or mania or any active major psychiatric disorder 5. recent (within 30 days) use of any cannabinoid (natural or synthetic) identified by self-report or urine drug screen for cannabinoids 6. taking any medication with known interactions with THC or CBD via cytochrome P450 (CYP) CYP2C9, CYP2C19 and CYP4A6 or CYP2D4 (e.g. anti-epileptic drugs, calcineurin inhibitors, anti-fungal) 7. evidence of liver dysfunction (ALT less than 3 times upper limit of normal, bilirubin below upper limit of normal, international normalized ratio\<1.5) 8. pregnant or breastfeeding women 9. change in ideal body weight or dry weight in the last 4 weeks 10. intradialytic hypotension (systolic blood pressure\<90mmHg) requiring an intervention in the previous 4 weeks

Design outcomes

Primary

MeasureTime frameDescription
Other cannabinoids and their metabolites dialytic clearance48 hoursDialytic clearance
Other cannabinoids and their metabolites last detection time48 hoursLast detection time
Other cannabinoids and their metabolites area under the curve48 hoursArea under the curve
Other cannabinoids and their metabolites renal clearance48 hoursRenal clearance
Tetrahydrocannabinol and its metabolites maximum concentration (Cmax)48 hoursMaximum concentration (Cmax)
Tetrahydrocannabinol and its metabolites time to Cmax48 hoursTime to Cmax
Tetrahydrocannabinol and its metabolites last detection time48 hoursLast detection time
Tetrahydrocannabinol and its metabolites area under the curve48 hoursArea under the curve
Tetrahydrocannabinol and its metabolites renal clearance48 hoursRenal clearance
Tetrahydrocannabinol and its metabolites dialytic clearance48 hoursDialytic clearance
Cannabidiol and its metabolites maximum concentration (Cmax)48 hoursMaximum concentration (Cmax)
Cannabidiol and its metabolites time to Cmax48 hoursTime to Cmax
Cannabidiol and its metabolites last detection time48 hoursLast detection time
Cannabidiol and its metabolites area under the curve48 hoursArea under the curve
Cannabidiol and its metabolites renal clearance48 hoursRenal clearance
Cannabidiol and its metabolites dialytic clearance48 hoursDialytic clearance
Other cannabinoids and their metabolites maximum concentration (Cmax)48 hoursMaximum concentration (Cmax)
Other cannabinoids and their metabolites time to Cmax48 hoursTime to Cmax

Secondary

MeasureTime frameDescription
Blood pressure48 hoursSystolic and diastolic blood pressure in mmHg
Heart rate48 hoursHeart rate in beats per minute
Adverse events48 hoursWeakness, fatigue, pain, falls, abnormal coordination, numbness or tingling, sedation, sleepiness, tremor, confusion, disorientation, dissociation, abnormal speech, muscle spasms, nausea, vomiting, diarrhea, altered mood, depression, euphoric mood, hallucinations, blurred vision, dizziness, imbalance, palpitations, hypotension, syncope, urinary tract infection, allergic reactions, shortness of breath, lung infection, fever, sweatiness, headache

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026