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Interactions Between Cannabinoids and Cytochrome P450-Metabolized Drugs

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Prisijungti Registracija
Nuoroda įrašoma į mainų sritį
StatusasKol kas neužverbuoja
Rėmėjai
Johns Hopkins University
Bendradarbiai
Washington State University
National Center for Complementary and Integrative Health (NCCIH)

Raktažodžiai

Santrauka

This study will evaluate drug-drug interactions between cannabis extracts containing Tetrahydrocannabinol (THC) and THC+ Cannabinoids (CBD) and probe drugs for select CYP450 pathways including: caffeine (CYP1A2), omeprazole (CYP2C19), losartan (CYP2C9), dextromethorphan (CYP2D6), and midazolam (CYP3A).

apibūdinimas

Despite the widespread use and availability of cannabis products, substantive deficiencies remain regarding the potential risks for cannabis or cannabinoids to precipitate adverse interactions with conventional drugs. Evidence from the few systematic clinical studies that have been conducted suggests that THC and CBD can inhibit metabolism of other drugs, via interactions with cytochrome P450 (CYP) enzymes, a large family of enzymes involved in the metabolism of numerous drugs and foreign chemicals in the body. Accordingly, evaluating the potential for drug-drug interactions between cannabis-derived products and common CYP-metabolized drugs merits further investigation. This double-blind, randomized crossover design study will evaluate whether, and to what extent, oral administration of cannabis extracts containing high doses of CBD and/or THC alter the pharmacokinetics of 5 drugs metabolized via CYP pathways including: caffeine (CYP1A2), omeprazole (CYP2C19), losartan (CYP2C9), dextromethorphan (CYP2D6), and midazolam (CYP3A). Healthy adults will complete three experimental dosing sessions, in which participants will orally ingest brownies containing (1) a high THC cannabis extract with a target THC dose of 40mg, (2) a high CBD cannabis extract with a target CBD dose of 1350mg + a THC dose of 40mg, or (3) placebo. In all three experimental dosing sessions, consumption of the cannabis extract infused brownie will be followed by ingestion of a drug "cocktail" comprised of commercial formulations of therapeutic or subtherapeutic doses of each drug. This collection of probe drugs, coined the Inje Cocktail, has been demonstrated to be safe, both administered alone and with various CYP450 inhibitors. At baseline and following administration of the study drugs, a battery of subjective, physiological, and cognitive performance assessments will be completed and biological specimens obtained. Each session will consist of a 12-hour outpatient drug administration visit and a 1-hour outpatient visit the subsequent day for additional biospecimen collection, cognitive testing, and subjective drug effect questionnaires. The study will conclude when 18 participants complete all 3 experimental sessions. The outcomes of this study will be useful to inform clinical decision-making regarding co-administration of cannabinoid-containing products with drugs that are either commonly prescribed by physicians or readily available over-the-counter.

Datos

Paskutinį kartą patikrinta: 03/31/2020
Pirmasis pateikimas: 12/12/2019
Numatytas registravimas pateiktas: 12/12/2019
Pirmas paskelbtas: 12/16/2019
Paskutinis atnaujinimas pateiktas: 04/08/2020
Paskutinis atnaujinimas paskelbtas: 04/09/2020
Faktinė studijų pradžios data: 07/31/2020
Numatoma pirminio užbaigimo data: 01/31/2021
Numatoma studijų užbaigimo data: 01/31/2021

Būklė ar liga

Drug-Interactions

Intervencija / gydymas

Drug: Inje cocktail

Drug: Inje Cocktail + THC extract

Drug: Inje Cocktail + THC/CBD extract

Fazė

Fazė 1

Rankų grupės

RankaIntervencija / gydymas
Active Comparator: Inje Cocktail
Single oral administration of caffeine (100mg), omeprazole (20mg), losartan (25mg), dextromethorphan (30mg), and midazolam (1mg)
Experimental: Inje Cocktail + THC extract
Single oral administration of Inje Cocktail + brownie infused with cannabis extract containing 40mg THC
Drug: Inje Cocktail + THC extract
Acute drug exposure
Experimental: Inje Cocktail + THC/CBD extract
Single oral administration of Inje Cocktail + brownie infused with cannabis extract containing 40mg THC and 1350mg CBD
Drug: Inje Cocktail + THC/CBD extract
Acute drug exposure

Tinkamumo kriterijai

Amžius, tinkami studijuoti 18 Years Į 18 Years
Tinkamos studijoms lytysAll
Priima sveikus savanoriusTaip
Kriterijai

Inclusion Criteria:

- Healthy adult between 18-50 years old

- BMI between 18 to 34 kg/m2

- Willing to use birth control

- Willing to abstain from all medications and citrus fruits for the duration of the study

Exclusion Criteria:

- Medical or psychiatric illness judged by the investigator to put the participant at greater risk of experiencing an adverse event due to drug exposure or completion of other study procedures.

- Use of medications which, in the opinion of the investigator or medical staff, will interfere with the study outcomes or the safety of the participant.

- Clinically significant impairment of kidney, liver, or thyroid function (serum creatinine >1.2 mg/ml (kidney), liver function tests >3x the upper limit of normal (alanine amino transferase >99 U/L; aspartate amino transferase > 99 U/L), and thyroid stimulating hormone > 4.2 uIU/ml), or evidence of current anemia based on blood chemistry testing.

- History of adverse events associated with the ingestion of cannabis or any medications in the Inje cocktail judged by the investigator to present an undue risk of harm to the participant.

Rezultatas

Pirminės rezultatų priemonės

1. Losartan Area Under the Curve (AUC) in plasma [24 hours]

Area under the curve concentration (mg/mL) of losartan in plasma

Antrinės rezultatų priemonės

1. Caffeine AUC in plasma [24 hours]

Area under the curve concentration (mg/mL) of caffeine in plasma

2. Omeprazole AUC in plasma [24 hours]

Area under the curve concentration (mg/mL) of omeprazole in plasma

3. Dextromethorphan AUC in plasma [24 hours]

Area under the curve concentration (mg/mL) of dextromethorphan in plasma

4. Midazolam AUC in plasma [24 hours]

Area under the curve concentration (mg/mL) of midazolam in plasma

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