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临床试验/NL-OMON46290
NL-OMON46290已完成不适用

An open-label, multi-centre drug-drug interaction trial to investigate the effects of tralokinumab on the pharmacokinetics of selected cytochrome P450 (CYP) substrates in adult subjects with moderate-to-severe atopic dermatitis - Drug-drug interaction tralokinumab in moderate-to-severe atopic dermatitis

eo Pharma0 个研究点目标入组 10 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 64(—)

入选标准

  • * Age 18 and above.
  • * Diagnosis of AD as defined by the Hanifin and Rajka 1980 criteria for AD.
  • * History of AD for *1 year.
  • * Subjects who have a recent history of inadequate response to treatment with topical medications or for whom topical treatments are otherwise medically inadvisable.
  • * AD involvement of *10% body surface area at screening and baseline.
  • * Stable dose of emollient twice daily (or more, as needed) for at least 14 days before baseline.
  • * Willingness to abstain from consumption of any 1 or more of the following items in the periods specified:
  • o ±7 days within each cocktail dosing visit (that is, between the Day -14 and Day 15 visits and between the Week 14 and Week 16 visits): foods/beverages that affect the CYP system:
  • - Grapefruit or grapefruit juice, Seville oranges or orange juice, starfruit, pomegranate and cranberry juices, red wine, red grape extract.
  • - Cruciferous vegetables, including but not limited to broccoli, cabbage, cauliflower, kale, Brussels sprout, radish, turnip, horseradish.
  • - Chargrilled meat.
  • o ±48 hours within each cocktail dosing visit: caffeinated beverages, foods/drugs that contain caffeine, including coffee, tea (black and green), coca cola, energy drinks, and chocolate.

排除标准

  • * Administration, within 14 days or 5 half-lives (whichever is longer) prior to Day -7, of any medication that is a known inducer or inhibitor of 1 or more of the following CYP enzymes: CYP3A, CYP2C19, CYP2C9, CYD2D6, and CYP1A2.
  • * Subjects who are poor metabolisers of CYP2C9, CYP2C19, or CYP2D6, based on genotyping.
  • * Any contraindication to 1 or more of the following drugs, according to the applicable labelling: caffeine, warfarin, omeprazole, metoprolol, or midazolam.
  • * Consumption of any 1 or more of the following items in the periods specified:
  • o From Day -14 (±7 days within each cocktail dosing visit):
  • foods/beverages that affect the CYP system:
  • - Grapefruit or grapefruit juice, Seville oranges or orange juice, starfruit, pomegranate and cranberry juices, red wine, red grape extract.
  • - Cruciferous vegetables, including but not limited to broccoli, cabbage, cauliflower, kale, Brussels sprout, radish, turnip, horseradish.
  • - Chargrilled meat.
  • o From Day -9 (±48 hours within each cocktail dosing visit):
  • caffeinated beverages, foods/drugs that contain caffeine, including coffee, tea (black and green), coca cola, energy drinks, and chocolate.
  • * Nausea or diarrhoea 1 week prior to Day -7.
  • * Active dermatologic conditions that may confound the diagnosis of AD.
  • * Use of tanning beds or phototherapy within 5 weeks prior to Day -7.
  • * Treatment with systemic immunosuppressive/immunomodulating drugs and/or systemic corticosteroid within 3 weeks prior to Day -7.
  • * Treatment with topical corticosteroids, topical calcineurin inhibitors, or topical phosphodiesterase 4 inhibitors within 1 week prior to Day -7.
  • * Receipt of any marketed biological therapy (that is, immunoglobulin or anti-immunoglobulin E) including dupilumab or investigational biologic agents:
  • o Any cell-depleting agents, including but not limited to rituximab: within 6 months prior to baseline (Day -7), or until lymphocyte count returns to normal, whichever is longer.
  • o Other biologics: within 3 months or 5 half-lives, whichever is longer, prior to baseline (Day -7).
  • * Active skin infection within 1 week prior to Day -7.
  • * Clinically significant infection within 4 weeks prior to Day -7.
  • * A helminth parasitic infection within 6 months prior to the date informed consent is obtained.
  • * Tuberculosis requiring treatment within the 12 months prior to screening.
  • * Known primary immunodeficiency disorder.

研究者

发起方
eo Pharma

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