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Drug-drug Interaction Trial With Tralokinumab in Moderate to Severe Atopic Dermatitis - ECZTRA 4

Primary Purpose

Atopic Dermatitis

Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
Tralokinumab
Caffeine
Warfarin
Omeprazole
Metoprolol
Midazolam Hydrochloride
Sponsored by
LEO Pharma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atopic Dermatitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Arm Label

All subjects

Arm Description

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.

Outcomes

Primary Outcome Measures

Ratio of the AUC-last at Week 15 (after multiple doses of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
AUC-last = area under the plasma concentration curve from time 0 to the last quantifiable observation
Ratio of the Cmax at Week 15 (after multiple doses of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
Cmax = maximum observed plasma concentration

Secondary Outcome Measures

Ratio of the AUC-last on Day 8 (after a single dose of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
AUC-last = area under the plasma concentration curve from time 0 to the last quantifiable observation
Ratio of the Cmax on Day 8 (after a single dose of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
Cmax = maximum observed plasma concentration
Ratio of the AUC-inf on Day 8 (after a single dose of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
AUC-inf = area under the plasma concentration curve from time 0 to infinity
Number of adverse events
Presence of anti-drug antibodies (yes/no)

Full Information

First Posted
May 30, 2018
Last Updated
October 23, 2020
Sponsor
LEO Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT03556592
Brief Title
Drug-drug Interaction Trial With Tralokinumab in Moderate to Severe Atopic Dermatitis - ECZTRA 4
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
August 13, 2018 (Actual)
Primary Completion Date
March 16, 2020 (Actual)
Study Completion Date
June 20, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
LEO Pharma

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
All subjects
Arm Type
Experimental
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Tralokinumab
Intervention Description
Human recombinant monoclonal antibody of the IgG4 subclass that specifically binds to human IL-13 and blocks interaction with the IL-13 receptors. Presented as a liquid formulation for subcutaneous injection.
Intervention Type
Drug
Intervention Name(s)
Caffeine
Intervention Description
1x 100 mg tablet
Intervention Type
Drug
Intervention Name(s)
Warfarin
Intervention Description
2x 5 mg tablets
Intervention Type
Drug
Intervention Name(s)
Omeprazole
Intervention Description
1x 20 mg capsule
Intervention Type
Drug
Intervention Name(s)
Metoprolol
Intervention Description
1x 100 mg tablet
Intervention Type
Drug
Intervention Name(s)
Midazolam Hydrochloride
Intervention Description
1 mL of 2 mg/mL oral solution/syrup
Primary Outcome Measure Information:
Title
Ratio of the AUC-last at Week 15 (after multiple doses of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
Description
AUC-last = area under the plasma concentration curve from time 0 to the last quantifiable observation
Time Frame
Day -7 and Week 15
Title
Ratio of the Cmax at Week 15 (after multiple doses of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
Description
Cmax = maximum observed plasma concentration
Time Frame
Day -7 and Week 15
Secondary Outcome Measure Information:
Title
Ratio of the AUC-last on Day 8 (after a single dose of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
Description
AUC-last = area under the plasma concentration curve from time 0 to the last quantifiable observation
Time Frame
Day -7 and Day 8
Title
Ratio of the Cmax on Day 8 (after a single dose of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
Description
Cmax = maximum observed plasma concentration
Time Frame
Day -7 and Day 8
Title
Ratio of the AUC-inf on Day 8 (after a single dose of tralokinumab) to that on Day -7 (at baseline) for each of the 5 substrates
Description
AUC-inf = area under the plasma concentration curve from time 0 to infinity
Time Frame
Day -7 and Day 8
Title
Number of adverse events
Time Frame
From Day 1 up to Week 30
Title
Presence of anti-drug antibodies (yes/no)
Time Frame
From Day 1 up to Week 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical expert
Organizational Affiliation
LEO Pharma
Official's Role
Study Director
Facility Information:
Facility Name
LEO Pharma Investigational Site
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72212
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Rogers
State/Province
Arkansas
ZIP/Postal Code
72758
Country
United States
Facility Name
LEO Pharma Investigational Site
City
San Diego
State/Province
California
ZIP/Postal Code
92119
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Doral
State/Province
Florida
ZIP/Postal Code
33122
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Miami
State/Province
Florida
ZIP/Postal Code
33015
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Miami
State/Province
Florida
ZIP/Postal Code
33144
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Quincy
State/Province
Massachusetts
ZIP/Postal Code
02169
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Spartanburg
State/Province
South Carolina
ZIP/Postal Code
29303
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23502
Country
United States
Facility Name
LEO Pharma Investigational Site
City
Nice
ZIP/Postal Code
06202
Country
France
Facility Name
LEO Pharma Investigational Site
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
LEO Pharma Investigational Site
City
Leiden
ZIP/Postal Code
2333 ZC
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Drug-drug Interaction Trial With Tralokinumab in Moderate to Severe Atopic Dermatitis - ECZTRA 4

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