カンナビジオールとタクロリムスの薬物-遺伝子-栄養補助食品の相互作用
The information learned in these studies will help to inform doctors as to how to appropriately adjust doses of cannabidiol and tacrolimus in order to improve health outcomes and long-term treatment success for transplant recipients.
調査の概要
状態
詳細な説明
The commercial availability of cannabidiol, or CBD oil, has increased in the United Stated and this supplement has the potential to cause a variety of drug-drug interactions, including in solid organ transplant recipients who receive tacrolimus to prevent rejection. Through a series of pharmacokinetic and pharmacodynamics assays, this proposal will identify gene-drug and drug-drug interactions (DDI), including those that place transplant recipients at risk for increased toxicity related to their immunosuppression. The information learned in these studies will help to inform practitioners as to whether cannabidiol needs to be avoided in transplant recipients and how to appropriately adjust doses of CBD and immunosuppression in order to improve health outcomes and long-term treatment success in this high-risk population.
研究の種類
入学 (実際)
段階
- フェーズ 1
連絡先と場所
研究場所
-
-
Indiana
-
Indianapolis、Indiana、アメリカ、46202
- IU Health University Hospital
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Age 18-75
- Are judged healthy enough to participate as determined by and decided from a pre-enrollment screening session that includes medical history and laboratory tests such as blood and urine tests, and electrocardiography (EKG).
- Agree to refrain from taking any prescription medications, over-the-counter medications, and herbal, dietary, and alternative supplements that may interact with the metabolism of the study drugs at least 2 weeks prior to the start of the study and until study completion.
- Are willing to commit the time requested for this study
- Are willing to refrain from smoking or use of tobacco or marijuana for at least two weeks prior to and until the completion of the study (the entire study lasts for approximately 26 days).
Additional Criteria for the Healthy volunteer study:
• Have a GFR above 60 ml/min/1.73m2 with proteinuria less than 0.3 grams by urine protein to creatinine ratio or 24 hour urine collection
Additional Criteria for the CKD study:
- Have either:
- A GFR less than or equal to 60 ml/min/1.73m2 or
- The presence of greater than 0.3 grams of proteinuria by urine protein to creatinine ratio or 24 hour urine collection, but less than 3.5 gm of nephrotic range proteinuria as hypoalbuminemia may impact protein binding.
Exclusion Criteria:
- Unable to provide informed consent
- Have history of intolerance, allergic reactions (e.g. rash) or other forms of hypersensitivities to any of the study medications (tacrolimus or cannabidiol);
- Are currently taking sedative agents, including agents for insomnia
- Are underweight (body mass index (BMI) less than 18.5) or overweight [body mass index (BMI) greater than 35]
- Have a positive pregnancy serum or urine test obtained just prior to each study, or are breast feeding
- Are night shift workers
- Are on dialysis
- Have compromised liver function as defined by pre-screening bilirubin, AST and ALT testing including any elevation of bilirubin or AST/ALT more than 2x the upper limit of normal.
- Are not willing to refrain from smoking or use of marijuana for at least two weeks prior to and until the completion of the study
- Have a Hgb < 10.0 g/dL
- Have gastrointestinal (digestive) disorders such as persistent diarrhea or malabsorption that would interfere with the absorption of orally administered drugs
- Have a history of or current seizure disorder
- Are currently on immunosuppression or are immunosuppressed.
- Are recipients of a current allograft (heart, kidney, pancreas, liver, intestine, lung, stem cell transplant).
- Have baseline EKG readings that are abnormal that could place the patient at the high risk.
- Have alcohol (more than 4 alcoholic drinks per day on a regular basis) or drug abuse, including opioids, or have used tobacco products or marijuana within the past three months, and are unwilling or unable to stop taking these medications two weeks prior to and during the entire study period
- Have participated in a research study involving intensive blood sampling or have donated blood within the past two months
- Had an unplanned hospitalization in the last 6 months or two or more unplanned hospitalizations in the last 2 years.
- Are taking prescription medications, that may interfere with the metabolism of the study drugs (e.g., inhibitors or inducers of CYP3A4/5 or CYP2C19 or those that will displace protein binding of tacrolimus/cannabidiol). Interactions will be screened according to the Flockhart table.
- Are taking over-the-counter medications, herbal or dietary supplements, and alternative medicines that may interfere with the metabolism of the study drugs (e.g., inhibitors or inducers of CYP3A4/5 or CYP2C19 or those that will displace protein binding of tacrolimus/cannabidiol) that the subject is unwilling or unable to stop over the course of the study. Interactions will be screened according to the Flockhart table.
- Are students under supervision of any of the study investigators.
- Cannot commit the time requested for this study.
- Have a known CYP3A4 *22/*22 genotype
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:支持療法
- 割り当て:非ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ:慢性腎疾患のないCYP3A5発現者
|
5 mg once
他の名前:
Epidiolex 5 mg/kg
他の名前:
Epidiolex at up to 5 mg/kg twice daily (for 14 days) and tacrolimus 5 mg once on day 12 of period
他の名前:
|
|
アクティブコンパレータ:慢性腎疾患のないCYP3A5非発現者
|
5 mg once
他の名前:
Epidiolex 5 mg/kg
他の名前:
Epidiolex at up to 5 mg/kg twice daily (for 14 days) and tacrolimus 5 mg once on day 12 of period
他の名前:
|
|
アクティブコンパレータ:慢性腎臓病の CYP3A5 発現者
|
5 mg once
他の名前:
Epidiolex 5 mg/kg
他の名前:
Epidiolex at up to 5 mg/kg twice daily (for 14 days) and tacrolimus 5 mg once on day 12 of period
他の名前:
|
|
アクティブコンパレータ:慢性腎臓病のCYP3A5非発現者
|
5 mg once
他の名前:
Epidiolex 5 mg/kg
他の名前:
Epidiolex at up to 5 mg/kg twice daily (for 14 days) and tacrolimus 5 mg once on day 12 of period
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The AUC0-Infinity Ratio of Tacrolimus With Cannabidiol Divided by Tacrolimus Alone
時間枠:27 days
|
The primary outcome is the AUC0-Infinity ratio of tacrolimus with cannabidiol divided by tacrolimus alone between CYP3A5 expressers and non-expressers in subjects with and without chronic kidney disease (CKD). Tacrolimus whole blood concentrations were measured at 0, 20, 40, and 60 minutes and 2, 4, 6, 12, 24, 48, and/or 72 hours. |
27 days
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Cell Viability Ratio
時間枠:27 days
|
The hypothesis tested is that cannabidiol will reduce immune cell proliferation between Period 1 and Period 3. There is no comparison between CYP3A5 expressor groups intended for this outcome measure. Period 1 (pre-CBD or baseline measurement) and Period 3 (post-CBD or steady-state cannabidiol) will be compared in a subset of individuals undergoing this phenotyping. Cell viability was measured in peripheral blood mononuclear cells using CellTiter-Glo (Promega Corp., catalog G7570) on 96-well plates to quantify cell proliferation by adenosine triphosphate (ATP) detection using a Spectramax M5 system coupled with SoftMax Pro 5.2 (Molecular Devices). Values were calculated as a unitless ratio of luminescence (ATP detection) in the stimulated (CD3/CD28) condition normalized by the non-stimulated (No CD3/CD28) condition. |
27 days
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Michael Eadon, MD、Indiana University
- 主任研究者:Zeruesenay Desta, PhD、Indiana University
出版物と役立つリンク
一般刊行物
- Birdwell KA, Decker B, Barbarino JM, Peterson JF, Stein CM, Sadee W, Wang D, Vinks AA, He Y, Swen JJ, Leeder JS, van Schaik R, Thummel KE, Klein TE, Caudle KE, MacPhee IA. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for CYP3A5 Genotype and Tacrolimus Dosing. Clin Pharmacol Ther. 2015 Jul;98(1):19-24. doi: 10.1002/cpt.113. Epub 2015 Jun 3.
- Brown JD, Winterstein AG. Potential Adverse Drug Events and Drug-Drug Interactions with Medical and Consumer Cannabidiol (CBD) Use. J Clin Med. 2019 Jul 8;8(7):989. doi: 10.3390/jcm8070989.
- Gisch DL, Koyama S, Etkins J, So GC, Fehrenbach DJ, Lu JBL, Cheng YH, Ferreira RM, Rajadhyaksha E, McClara K, Asghari M, Sharfuddin AA, Dagher PC, Snell LM, Madhur MS, Polidoro RB, Desta Z, Eadon MT. Cannabidiol exerts antiinflammatory effects but maintains T effector memory cell differentiation in humans. JCI Insight. 2025 Nov 18;11(1):e198590. doi: 10.1172/jci.insight.198590. eCollection 2026 Jan 9.
- So GC, Lu JBL, Koyama S, Cheng YH, Gisch DL, McClara K, Dexter PR, Sharfuddin AA, Etkins J, Tillman EM, Beamon TR, Cowsert Z, Stuart JS, Desta Z, Eadon MT. A Phase I Trial of the Pharmacokinetic Interaction Between Cannabidiol and Tacrolimus. Clin Pharmacol Ther. 2025 Mar;117(3):716-723. doi: 10.1002/cpt.3504. Epub 2024 Nov 27.
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 12763
- 5R01AT011463-02 (米国 NIH グラント/契約)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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