ClinicalTrials.Veeva

Menu
The trial is taking place at:
A

Arke Estudios Clinicos S.A. de C.V. | Veracruz, Mexico

Veeva-enabled site

A Study of Baricitinib (LY3009104) in Children and Adolescents With Atopic Dermatitis (BREEZE-AD-PEDS)

Lilly logo

Lilly

Status and phase

Active, not recruiting
Phase 3

Conditions

Atopic Dermatitis

Treatments

Drug: Topical corticosteroid
Drug: Baricitinib
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT03952559
16966
2018-000349-38 (EudraCT Number)
I4V-MC-JAIP (Other Identifier)

Details and patient eligibility

About

The reason for this study is to see if the study drug called baricitinib works and is safe in children and teenage participants with atopic dermatitis.

Enrollment

516 patients

Sex

All

Ages

2 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • At or above the 5th percentile of weight for age.
  • Have been diagnosed with moderate to severe atopic dermatitis for at least 12 months (if 6 years old or older) or at least 6 months (if 2 up to 6 years old).
  • Have had inadequate response or intolerance to existing topical (applied to the skin) medications within 6 months preceding screening.
  • Are willing to discontinue certain treatments for eczema (such as systemic and topical treatments during a washout period).
  • Agree to use emollients daily.

Exclusion criteria

  • Are currently experiencing or have a history of other concomitant skin conditions (e.g., psoriasis or lupus erythematosus), or a history of erythrodermic, refractory, or unstable skin disease that requires frequent hospitalizations and/or intravenous treatment for skin infections.

  • A history of eczema herpeticum within 12 months, and/or a history of 2 or more episode of eczema herpeticum in the past.

  • Participants who are currently experiencing a skin infection that requires treatment, or is currently being treated, with topical or systemic antibiotics.

  • Have any serious illness that is anticipated to require the use of systemic corticosteroids or otherwise interfere with study participation or require active frequent monitoring (e.g., unstable chronic asthma).

  • Have been treated with the following therapies:

    • Monoclonal antibody for less than 5 half-lives prior to beginning study treatment.
    • Received prior treatment with any oral Janus kinase (JAK) inhibitor.
    • Received any parenteral corticosteroids administered by intramuscular or intravenous (IV) injection within 2 weeks prior to study entry or within 6 weeks prior to planned initiation of study drug or are anticipated to require parenteral injection of corticosteroids during the study.
  • Have had an intra-articular corticosteroid injection within 2 weeks prior to study entry or within 6 weeks prior to planned initiation of study drug.

  • Have high blood pressure characterized by a repeated systolic or diastolic blood pressure >95th percentile based on age, sex and height.

  • Have had major surgery within the past eight weeks or are planning major surgery during the study.

  • Have experienced any of the following within 12 weeks of screening: venous thromboembolic event (VTE), myocardial infarction (MI), unstable ischemic heart disease, stroke, or New York Heart Association Stage III/IV heart failure.

  • Have a history of VTE or are considered at high risk of VTE as deemed by the investigator.

  • Have a history or presence of cardiovascular, respiratory, hepatic, chronic liver disease gastrointestinal, endocrine, hematological, neurological, lymphoproliferative disease or neuropsychiatric disorders or any other serious and/or unstable illness.

  • Have a current or recent clinically serious viral, bacterial, fungal, or parasitic infection including herpes zoster (shingles or chicken pox), tuberculosis.

  • Have specific laboratory abnormalities.

  • Have received certain treatments that are contraindicated.

  • Pregnant or breastfeeding.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

516 participants in 5 patient groups, including a placebo group

Baricitinib Open Label High Dose (PK Lead-in)
Experimental group
Description:
Participants 10 to \< 18 years received Baricitinib high dose (4 mg) administered orally in tablet form QD. Participants 2 to \< 10 years received Baricitinib high dose (2 mg) administered as oral suspension (1 mL) QD.
Treatment:
Drug: Baricitinib
Drug: Topical corticosteroid
Baricitinib High Dose
Experimental group
Description:
Participants 10 to \< 18 years received Baricitinib high dose (4 mg) and placebo to maintain the blind, administered orally in tablet form QD. Participants 2 to \< 10 years received Baricitinib high dose (2 mg) administered as oral suspension QD or placebo oral suspension QD to maintain the blind.
Treatment:
Drug: Baricitinib
Drug: Topical corticosteroid
Baricitinib Medium Dose
Experimental group
Description:
Participants 10 to \< 18 years received Baricitinib low dose (1 mg) and placebo to maintain the blind, administered orally in tablet form QD. Participants 2 to \< 10 years received Baricitinib low dose (0.5 mg) administered as oral suspension QD or placebo oral suspension QD to maintain the blind.
Treatment:
Drug: Baricitinib
Drug: Topical corticosteroid
Baricitinib Low Dose
Experimental group
Description:
Participants 10 to \< 18 years received Baricitinib low dose (1 mg) and placebo to maintain the blind, administered orally in tablet form QD. Participants 2 to \< 10 years received Baricitinib low dose (0.5 mg) administered as oral suspension QD or placebo oral suspension QD to maintain the blind.
Treatment:
Drug: Baricitinib
Drug: Topical corticosteroid
Placebo
Placebo Comparator group
Description:
Participants 10 to \< 18 years received placebo tablets. Participants 2 to \< 10 years received placebo as oral suspension.
Treatment:
Drug: Placebo
Drug: Topical corticosteroid

Trial documents
2

Trial contacts and locations

79

Loading...

Central trial contact

There may be multiple sites in this clinical trial. 1-877-CTLILLY (1-877-285-4559) or

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems