Drug-drug Interaction Trial With Tralokinumab in Moderate to Severe Atopic Dermatitis - ECZTRA 4
Atopic Dermatitis
About this trial
This is an interventional treatment trial for Atopic Dermatitis
Eligibility Criteria
Inclusion Criteria:
- 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:
±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 (for example broccoli).
- Chargrilled meat.
- ±48 hours within each cocktail dosing visit: caffeinated beverages and foods/drugs that contain caffeine.
Exclusion Criteria:
- 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:
±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 (for example broccoli).
- Chargrilled meat.
- ±48 hours within each cocktail dosing visit: caffeinated beverages and foods/drugs that contain caffeine.
- 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 or investigational biologic agent (including immunoglobulin, anti-IgE, or dupilumab):
- Any cell-depleting agents, including but not limited to rituximab: within 6 months prior to Day -7, or until lymphocyte count returns to normal, whichever is longer.
- Other biologics: within 3 months or 5 half-lives, whichever is longer, prior to 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 12 months prior to screening.
- Known primary immunodeficiency disorder.
Sites / Locations
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
- LEO Pharma Investigational Site
Arms of the Study
Arm 1
Experimental
All subjects
Tralokinumab - investigational medicinal product: Week 0: subcutaneous (SC) injection of tralokinumab loading dose. Week 2 to Week 14: SC injection of tralokinumab maintenance dose. CYP substrates - non-investigational medicinal products: Week -1, Week 1, and Week 15: oral administration of caffeine 100 mg, warfarin sodium 5 mg x2, omeprazole 20 mg, metoprolol tartrate 100 mg, and midazolam hydrochloride 2 mg.