Drug-drug Interaction Trial With Tralokinumab in Moderate to Severe Atopic Dermatitis - ECZTRA 4
Status: | Recruiting |
---|---|
Conditions: | Psoriasis, Dermatology, Dermatology, Dermatology |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/26/2018 |
Start Date: | August 13, 2018 |
End Date: | October 1, 2019 |
Contact: | LEO Pharma A/S |
Email: | disclosure@leo-pharma.com |
Phone: | (+1) 877-557-1168 |
An Open-label, Multi Centre Drug-drug Interaction Trial to Investigate the Effects of Tralokinumab on the Pharmacokinetics of Selected Cytochrome P450 Substrates in Adult Subjects With Moderate-to-severe Atopic Dermatitis
The purpose of this trial is to investigate if tralokinumab changes the metabolism of
selected CYP substrates in adults with moderate-to-severe AD after:
- 14 weeks of treatment with tralokinumab
- a single dose of tralokinumab
selected CYP substrates in adults with moderate-to-severe AD after:
- 14 weeks of treatment with tralokinumab
- a single dose of tralokinumab
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.
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