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临床试验/NCT04840862
NCT04840862已完成4 期

Impact of Rifabutin on the Pharmacokinetics of Elexacaftor/Tezacaftor/Ivacaftor

University of Southern California1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2022年5月9日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
6
试验地点
1
主要终点
24h area-under the plasma concentration time curve (AUC) of ELX/TEZ/IVA in the absence and the presence of concomitant rifabutin

研究概览

简要总结

This is a prospective, single-center, fixed-sequence, nonrandomized, open-label study in healthy adults to investigate the impact of rifabutin on the pharmacokinetics of trikafta.

详细描述

Trikafta (Elexacaftor [ELX], Tezacaftor [TEZ], Ivacaftor[IVA]) is contraindicated with concomitant use of strong inducers as co-administration of rifampin decreased the area-under-the concentration time curve (AUC) of IVA by 89%, creating a therapeutic challenge to the treatment of non-tuberculosis mycobacteria (NTM) infection in people with cystic fibrosis (CF). While rifabutin also induces CYP3A4 activity, its effects appear to be more moderate when compared with rifampin. Therefore, we hypothesize that rifabutin can be co-administered with an adjusted dose of ELX/TEZ/IVA in patients being treated for NTM pulmonary disease.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Able and willing to sign informed consent prior to any study-related activities.
  • Male or female participants between 18 and 65 years of age inclusive.
  • Healthy subjects as determined by no clinically significant deviation from normal in medical history, physical examination findings, and clinical laboratory test results
  • Body mass index (BMI) of 17.5 to 30.5 kg/m2, inclusive; and a total body weight >50kg (110 lbs).
  • Willing to stop using any herbal or natural health products for 2 weeks prior to and during the study including: Grapefruit, grapefruit juice, St. John's Wort.
  • Participant must use a reliable method of birth control while they are participating in the study; for instance an intrauterine device (IUD), condom with spermicidal gel or foam, diaphragm with spermicidal gel or foam, vasectomy, tubal ligation, hysterectomy or abstinence or female must be post-menopausal for at least one year.

排除标准

  • Female subjects of childbearing potential with positive urine pregnancy test at screening.
  • Female subjects who are breastfeeding.
  • Use of CYP3A modulators (e.g., rifampicin, phenobarbital, carbamazepine, phenytoin, azole drugs, telithromycin, clarithromycin, erythromycin)
  • Any significant acute or chronic medical illness that might confound the results of the study or pose an additional risk in administrating study drugs to the subject, as determined by the investigator.
  • Any condition that could affect drug absorption (eg, gastrectomy, pancreatitis).
  • Any major surgery within 4 weeks of study drug administration.
  • Blood donation of approximately 1 pint (500 mL) within 56 days before study drug administration.
  • Known hypersensitivity to rifamycins
  • Patients with hepatic impairment (Child-Pugh Class B or C) and/or with history of hepatobiliary disease or liver function test elevations.
  • Renal insufficiency (eGFR < 60 mL/min)
  • History of uveitis and/or current eye or vision problems with the exception of corrective lenses.
  • Contact lens use during study drug administration.

研究组 & 干预措施

rifabutin

Experimental

Rifabutin PO [two 150mg capsules] ; Trikafta PO [one orange tablet containing ELX 100mg, TEZ 50mg, and IVA 75mg]

干预措施: Trikafta [orange tablet containing ELX 100mg, TEZ 50mg, and IVA 75mg] (Drug)

rifabutin

Experimental

Rifabutin PO [two 150mg capsules] ; Trikafta PO [one orange tablet containing ELX 100mg, TEZ 50mg, and IVA 75mg]

干预措施: Rifabutin 300mg (Drug)

结局指标

主要结局

24h area-under the plasma concentration time curve (AUC) of ELX/TEZ/IVA in the absence and the presence of concomitant rifabutin

时间窗: 22 days

To assess the impact of rifabutin on the AUC of ELX/TEZ/IVA

次要结局

  • Maximum plasma concentration (Cmax) of ELX/TEZ/IVA in the absence and the presence of concomitant rifabutin(22 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paul Beringer

Professor of Clinical Pharmacy

University of Southern California

研究点 (1)

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