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| ID | Type | Description | Link |
|---|---|---|---|
| U54AT008909 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| Office of Dietary Supplements (ODS) | NIH |
| National Center for Complementary and Integrative Health (NCCIH) | NIH |
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The goal of this clinical trial is to determine how two different doses of cannabidiol (CBD), given as a hemp product, change the blood concentrations of the drug clopidogrel in the body. Results will be used to help design future studies and to assist healthcare providers in informing their patients about the safe use of CBD.
The popularity of cannabis products has grown exponentially over the past decade as several states continue to decriminalize or legalize recreational and/or medicinal use. Cannabis contains >500 phytoconstituents, including >100 cannabinoids. The most well-studied cannabinoids are tetrahydrocannabinol (THC) and cannabidiol (CBD). Although both are psychoactive, THC produces the characteristic "high," while CBD does not. CBD is available as a prescription drug (Epidiolex®) to treat seizure disorders. Hemp, a popular CBD-containing botanical product, is defined as containing <0.3% THC. Hemp was federally legalized in the United States in 2018 following passage of the Farm Bill. Since passage of that bill, hemp and other CBD-containing products have become widely available over the counter. As such, hemp/CBD products have become top-selling botanicals, with sales projected to reach nearly $4.5 billion by 2024. Common uses include self-treatment for pain, anxiety, and sleep disorders.
Despite increasing use of cannabis products, the pharmacokinetic interaction potential with pharmaceutical medications remains understudied. Previous pharmacokinetic studies have yielded convincing evidence that CBD significantly inhibits the activity of the drug metabolizing enzyme cytochrome P450 (CYP) 2C19. Despite the valuable information generated by these and numerous other studies, several unanswered questions about CBD-containing products remain:
The primary objective of the proposed study is to evaluate the effects of a well-characterized, widely used hemp product on the pharmacokinetics of the commonly prescribed CYP2C19 substrate clopidogrel (Plavix®) in healthy adult participants who are confirmed to be CYP2C19 normal, rapid, or ultra-rapid metabolizers. Results could be used to inform a future study design involving elderly people, which is a population of interest. Results could also be used to guide healthcare providers in helping their patients make informed decisions about the safe use of hemp
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm 1: clopidogrel alone | Experimental | Participants will be administered a single oral dose (75 mg) of clopidogrel. Blood and urine will be collected for 24 hours. |
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| Arm 2: chronic hemp (30 mg CBD) + clopidogrel | Experimental | Participants will self-administer a single low dose of hemp (30 mg CBD) as an oral softgel at home daily for 5 consecutive days. On day 6, participants will return to the research setting, where they will be administered a single low dose of hemp (30 mg CBD) and a single oral dose of clopidogrel (75 mg). Blood will be collected for 72 hours and urine will be collected for 24 hours. |
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| Arm 3: chronic hemp (240 mg CBD) + clopidogrel | Experimental | Participants will repeat the Arm 2 procedures using a higher dose of hemp (240 mg CBD) |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cannabidiol in the form of hemp | Drug | Cannabidiol (30 mg) in the form of an orally administered hemp oil softgel |
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| Measure | Description | Time Frame |
|---|---|---|
| AUC ratio of clopidogrel active metabolite | Ratio of the area under the plasma concentration vs. time curve of the active metabolite of clopidogrel in the presence to absence of hemp | 0-24 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Cannabidiol AUC | Area under the plasma concentration vs. time curve of cannabidiol | 0-72 hours |
| AUC of cannabidiol metabolites | Area under the plasma concentration vs. time curve of cannabidiol metabolites |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Mary F Paine, RPh, PhD | Contact | 509-358-7759 | mary.paine@wsu.edu |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Washington State University College of Pharmacy and Pharmaceutical Sciences | Recruiting | Spokane | Washington | 99202 | United States |
IPD used in the results publication
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| ID | Term |
|---|---|
| D002185 | Cannabidiol |
| D000077144 | Clopidogrel |
| ID | Term |
|---|---|
| D002186 | Cannabinoids |
| D013729 | Terpenes |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
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| Clopidogrel | Drug | 75 mg oral clopidogrel |
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| 0-72 hours |
| D013988 |
| Ticlopidine |
| D058924 | Thienopyridines |
| D013876 | Thiophenes |
| D013457 | Sulfur Compounds |
| D011725 | Pyridines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |