A Study of Baricitinib (LY3009104) in Patients With Moderate to Severe Atopic Dermatitis

NCT ID: NCT03334396

Last Updated: 2020-08-18

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

660 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-11-23

Study Completion Date

2019-08-16

Brief Summary

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The purpose of this study is to evaluate the efficacy and safety of baricitinib as monotherapy in participants with moderate to severe atopic dermatitis.

Detailed Description

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Conditions

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Atopic Dermatitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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4 milligram (mg) Baricitinib

4 mg Baricitinib administered orally once daily. Placebo 1 mg and 2 mg administered orally every day to match.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally.

Placebo

Intervention Type DRUG

Administered orally.

2 mg Baricitinib

2 mg Baricitinib administered orally once daily. Placebo 1 mg and 4 mg administered orally every day to match.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally.

Placebo

Intervention Type DRUG

Administered orally.

1 mg Baricitinib

1 mg Baricitinib administered orally once daily. Placebo 2 mg and 4 mg administered orally every day to match.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally.

Placebo

Intervention Type DRUG

Administered orally.

Placebo

Placebo administered orally once daily.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Administered orally.

4 mg Baricitinib Maximum Extended Enrollment Cohort

4 mg Baricitinib administered orally once daily. Placebo 1 mg, and 2 mg administered orally every day to match.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally.

Placebo

Intervention Type DRUG

Administered orally.

2 mg Baricitinib Maximum Extended Enrollment Cohort

2 mg Baricitinib administered orally once daily. Placebo 1 mg and 4 mg administered orally every day to match.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally.

Placebo

Intervention Type DRUG

Administered orally.

1 mg Baricitinib Maximum Extended Enrollment Cohort

1 mg Baricitinib administered orally once daily. Placebo 2 mg and 4 mg administered orally every day to match.

Group Type EXPERIMENTAL

Baricitinib

Intervention Type DRUG

Administered orally.

Placebo

Intervention Type DRUG

Administered orally.

Placebo Maximum Extended Enrollment Cohort

Placebo administered orally once daily.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Administered orally.

Interventions

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Baricitinib

Administered orally.

Intervention Type DRUG

Placebo

Administered orally.

Intervention Type DRUG

Other Intervention Names

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LY3009104

Eligibility Criteria

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Inclusion Criteria

* Have been diagnosed with moderate to severe Atopic Dermatitis for at least 12 months.
* 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 randomization.
* 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 randomization 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 randomization.
* Have high blood pressure characterized by a repeated systolic blood pressure \>160 millimeters of mercury (mm Hg) or diastolic blood pressure \>100 mm Hg.
* 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 recurrent (≥ 2) 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, tuberculosis.
* Have specific laboratory abnormalities.
* Have received certain treatments that are contraindicated.
* Pregnant or breastfeeding.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Incyte Corporation

INDUSTRY

Sponsor Role collaborator

Eli Lilly and Company

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Role: STUDY_DIRECTOR

Eli Lilly and Company

Locations

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Kozni ambulance Kutna Hora, s.r.o.

Kutná Hora, Central Bohemia, Czechia

Site Status

Clintrial, s.r.o.

Prague, Hl. M. Praha, Czechia

Site Status

Fakultni nemocnice Kralovske Vinohrady

Prague, Hl. M. Praha, Czechia

Site Status

Fakultni Nemocnice v Motole

Prague, Hl. M. Praha, Czechia

Site Status

Nemocnice Na Bulovce

Prague, Hl. M. Praha, Czechia

Site Status

Nemocnice Novy Jicin a.s.

Nový Jičín, Moravskoslezský kraj, Czechia

Site Status

Fakultni Nemocnice Plzen

Plzen, Jizni Predmesti, Plzeň Region, Czechia

Site Status

Fakultni Nemocnice U svate Anny

Brno, South Moravian, Czechia

Site Status

Krajska zdravotni a.s. - Masarykova nemocnice v Usti nad Labem, o.z.

Ústí nad Labem, Ustecký Kraj, Czechia

Site Status

Aarhus Universitehospital Marselisborg Centret

Aarhus, , Denmark

Site Status

Hopital Saint-Louis

Paris, Cedex 10, France

Site Status

CHU de Bordeaux Hopital Saint Andre

Bordeaux, , France

Site Status

CHRU de Brest - Hôpital Morvan

Brest, , France

Site Status

CHU Grenoble Alpes

Grenoble Cédex 9, , France

Site Status

Chru De Nantes Hotel-Dieu

Nantes, , France

Site Status

CHU de Nice Hopital de L'Archet

Nice, , France

Site Status

Centre Hospitalier Lyon Sud

Pierre-Bénite, , France

Site Status

Hopital Larrey

Toulouse, , France

Site Status

Universitätsklinikum Freiburg

Freiburg im Breisgau, Baden-Wurttemberg, Germany

Site Status

Klinikum der Universität München

München, Bavaria, Germany

Site Status

Gemeinschaftspraxis Mahlow

Blankenfelde-Mahlow, Brandenburg, Germany

Site Status

Rosenpark Research Geschäftsbereich der Rosenparkklinik GmbH

Darmstadt, Hesse, Germany

Site Status

Klinikum der Johann Wolfgang Goethe-Universität Frankfurt

Frankfurt am Main, Hesse, Germany

Site Status

Dermatologisches Zentrum Osnabrück Nord

Bramsche, Lower Saxony, Germany

Site Status

Universitätsmedizin Göttingen

Göttingen, Lower Saxony, Germany

Site Status

Universitätsmedizin Rostock

Rostock, Mecklenburg-Vorpommern, Germany

Site Status

Universitätsklinikum Bonn

Bonn, North Rhine-Westphalia, Germany

Site Status

Praxis Dr. Thomas Dirschka

Wuppertal, North Rhine-Westphalia, Germany

Site Status

Praxis Gerlach

Dresden, Saxony, Germany

Site Status

Universitätsklinikum Carl Gustav Carus

Dresden, Saxony, Germany

Site Status

Universität Leipzig - Universitätsklinikum

Leipzig, Saxony, Germany

Site Status

Universitätsklinikum Otto-von-Guericke-Universität

Magdeburg, Saxony-Anhalt, Germany

Site Status

Hautarztzentrum Kiel

Kiel, Schleswig-Holstein, Germany

Site Status

Universitätsklinikum Schleswig-Holstein

Kiel, Schleswig-Holstein, Germany

Site Status

Universitätsklinikum Schleswig-Holstein

Lübeck, Schleswig-Holstein, Germany

Site Status

Rothhaar Studien GmbH

Berlin, , Germany

Site Status

ISA GmbH

Berlin, , Germany

Site Status

Praxis für Ganzheitliche Dermatologie im Ärztehaus

Berlin, , Germany

Site Status

TFS Trial Form Support GmbH

Hamburg, , Germany

Site Status

King George Hospital

Vizag, Andhra Pradesh, India

Site Status

Panchshil Hospital

Ahmedabad, Gujarat, India

Site Status

Byramjee Jeejeebhoy Medical College & Civil Hospital

Ahmedabad, Gujarat, India

Site Status

M S Ramaiah Medical College Hospital

Bangalore, Karnataka, India

Site Status

Dr. D. Y. Patil Medical College & Hospital

Navi Mumbai, Maharashtra, India

Site Status

Jehangir Hospital

Pune, Maharashtra, India

Site Status

Seth GS Medical College & KEM Hospital

Mumbai, Maharshtra, India

Site Status

All India Institue of Medical Sciences (AIIMS)

New Delhi, National Capital Territory of Delhi, India

Site Status

Sir Ganga Ram Hospital

New Delhi, National Capital Territory of Delhi, India

Site Status

Chennai Meenakshi Multispeciality Hospital

Chennai, Tamil Nadu, India

Site Status

Gandhi Hospital

Secunderabad, Telangana, India

Site Status

MV Hospital and Research Centre

Lucknow, Uttar Pradesh, India

Site Status

Istituto Clinico Humanitas

Rozzano, Milano, Italy

Site Status

Azienda Ospedaliera Universitaria Federico II

Napoli, , Italy

Site Status

Azienda Ospedaliera - Universitaria Pisana

Pisa, , Italy

Site Status

Policlinico di Tor Vergata

Roma, , Italy

Site Status

Ospedale Policlinico Giambattista Rossi, Borgo Roma

Verona, , Italy

Site Status

Kawashima Dermatology Clinic

Ichikawa-shi, Chiba, Japan

Site Status

Fumimori Clinic

Fukuoka, Fukuoka, Japan

Site Status

Hiroshima University Hospital

Hiroshima, Hiroshima, Japan

Site Status

Queen's Square Dermatology and Allergology

Nishi-ku, Yokohama-city, Kanagawa, Japan

Site Status

Yokohama City Minato Red Cross Hospital

Yokohama, Kanagawa, Japan

Site Status

Kyoto Prefectural University of Medicine

Kyoto, Kyoto, Japan

Site Status

Kume Clinic

Nishi-ku Sakai-shi, Osaka, Japan

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Shimane University Hospital

Izumo, Shimane, Japan

Site Status

JA Shizuoka Kohseiren Enshu Hospital

Hamamatsu, Shizuoka, Japan

Site Status

Iidabashi Clinic

Chiyoda-ku, Tokyo, Japan

Site Status

Nihonbashi Sakura Clinic

Chuo-ku, Tokyo, Japan

Site Status

Sumire Dermatology Clinic

Edogawa-ku, Tokyo, Japan

Site Status

NTT Medical Center Tokyo

Shinagawa-KU, Tokyo, Japan

Site Status

Shirasaki Clinic

Takaoka-shi, Toyama, Japan

Site Status

Yamanashi Prefectural Central Hospital

Kofu, Yamanashi, Japan

Site Status

Fukuoka University Hospital

Fukuoka, , Japan

Site Status

Grupo Médico CAMINO S.C.

Mexico City, Mexico City, Mexico

Site Status

Hospital de Jesus I.A.P.

Mexico City, Mexico City, Mexico

Site Status

Clínica Enfermedades Crónicas y Procedimientos Especiales SC

Morella, Michoacán, Mexico

Site Status

CRI Centro Regiomontano de Investigacion S.C.

Monterrey, Nuevo León, Mexico

Site Status

Hospital Univ. Dr. Jose Eleuterio Gonzalez

Monterrey, Nuevo León, Mexico

Site Status

JM Research S.C.

Cuernavaca, , Mexico

Site Status

RM Pharma Specialists S.A. de C.V.

Distrito Federal, , Mexico

Site Status

Instituto de Investigaciones Aplicadas a la Neurociencia A.C

Durango, , Mexico

Site Status

GBUZ Clinical dermatology and venereological dispensary

Krasnodar, , Russia

Site Status

State scientific centre for dermatovenerology and cosmetolog

Moscow, , Russia

Site Status

Russian state medical-stomatological university n.a. Evdokimov

Moscow, , Russia

Site Status

SPb SBHI Skin-venerologic dispensary #10

Saint Petersburg, , Russia

Site Status

LLC ArsVitae NorthWest

Saint Petersburg, , Russia

Site Status

LLC Medical Center "Kurator"

Saint Petersburg, , Russia

Site Status

Chang Gung Memorial Hospital - Kaohsiung

Kaohsiung City, , Taiwan

Site Status

Taipei Medical University- Shuang Ho Hospital

New Taipei City, , Taiwan

Site Status

Chung Shan Medical University Hospital

Taichung, , Taiwan

Site Status

National Cheng Kung University Hospital

Tainan City, , Taiwan

Site Status

National Taiwan University Hospital

Taipei, , Taiwan

Site Status

Chang Gung Memorial Hospital - Taipei

Taipei, , Taiwan

Site Status

Chang Gung Memorial Hospital - Linkou

Taoyuan, , Taiwan

Site Status

Countries

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Czechia Denmark France Germany India Italy Japan Mexico Russia Taiwan

References

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Katoh N, Takita Y, Isaka Y, Nishikawa A, Torisu-Itakura H, Saeki H. Pooled Safety Analysis of Baricitinib in Adult Participants with Atopic Dermatitis in the Japanese Subpopulation from Six Randomized Clinical Trials. Dermatol Ther (Heidelb). 2022 Dec;12(12):2765-2779. doi: 10.1007/s13555-022-00828-5. Epub 2022 Oct 18.

Reference Type DERIVED
PMID: 36255569 (View on PubMed)

Silverberg JI, DeLozier A, Sun L, Thyssen JP, Kim B, Yosipovitch G, Nunes FP, Gugiu PC, Doll HA, Eichenfield LF. Psychometric properties of the itch numeric rating scale, skin pain numeric rating scale, and atopic dermatitis sleep scale in adult patients with moderate-to-severe atopic dermatitis. Health Qual Life Outcomes. 2021 Oct 23;19(1):247. doi: 10.1186/s12955-021-01877-8.

Reference Type DERIVED
PMID: 34688290 (View on PubMed)

Thyssen JP, Buhl T, Fernandez-Penas P, Kabashima K, Chen S, Lu N, DeLozier AM, Casillas M, Stander S. Baricitinib Rapidly Improves Skin Pain Resulting in Improved Quality of Life for Patients with Atopic Dermatitis: Analyses from BREEZE-AD1, 2, and 7. Dermatol Ther (Heidelb). 2021 Oct;11(5):1599-1611. doi: 10.1007/s13555-021-00577-x. Epub 2021 Jul 18.

Reference Type DERIVED
PMID: 34275122 (View on PubMed)

King B, Maari C, Lain E, Silverberg JI, Issa M, Holzwarth K, Brinker D, Cardillo T, Nunes FP, Simpson EL. Extended Safety Analysis of Baricitinib 2 mg in Adult Patients with Atopic Dermatitis: An Integrated Analysis from Eight Randomized Clinical Trials. Am J Clin Dermatol. 2021 May;22(3):395-405. doi: 10.1007/s40257-021-00602-x. Epub 2021 Apr 7.

Reference Type DERIVED
PMID: 33826132 (View on PubMed)

Reich K, DeLozier AM, Nunes FP, Thyssen JP, Eichenfield LF, Wollenberg A, Ross Terres JA, Watts SD, Chen YF, Simpson EL, Silverberg JI. Baricitinib improves symptoms in patients with moderate-to-severe atopic dermatitis and inadequate response to topical corticosteroids: patient-reported outcomes from two randomized monotherapy phase III trials. J Dermatolog Treat. 2022 May;33(3):1521-1530. doi: 10.1080/09546634.2020.1839008. Epub 2020 Nov 22.

Reference Type DERIVED
PMID: 33222559 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Related Links

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https://www.lillytrialguide.com/en-US/studies/eczema/JAHL#?postal=

A Study of Baricitinib (LY3009104) in Adults With Moderate to Severe Atopic Dermatitis (Eczema) (BREEZE-AD1)

Other Identifiers

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I4V-MC-JAHL

Identifier Type: OTHER

Identifier Source: secondary_id

2017-000870-12

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

16580

Identifier Type: -

Identifier Source: org_study_id

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