Chovatiya, Raj https://orcid.org/0000-0001-6510-399X
Ribero, Simone
Wollenberg, Andreas
Park, Chang Ook
Silvestre, Juan Francisco
Hong, H. Chih-Ho
Seneschal, Julien
Saeki, Hidehisa
Thyssen, Jacob P.
Øland, Christian Bjerregård
Gjerum, Le
Maslin, Douglas
Blauvelt, Andrew
Clinical trials referenced in this document:
Documents that mention this clinical trial
Tralokinumab Efficacy and Safety, with or without Topical Corticosteroids, in North American Adults with Moderate-to-Severe Atopic Dermatitis: A Subanalysis of Phase 3 Trials ECZTRA 1, 2, and 3
https://doi.org/10.1007/s13555-022-00805-y
Long-Term Disease Control and Minimal Disease Activity of Head and Neck Atopic Dermatitis in Patients Treated with Tralokinumab up to 4 Years
https://doi.org/10.1007/s40257-025-00931-1
Tralokinumab Efficacy Over 1 Year in Adults with Moderate-to-Severe Atopic Dermatitis: Pooled Data from Two Phase III Trials
https://doi.org/10.1007/s40257-023-00806-3
Tralokinumab Provides Clinically Meaningful Responses at Week 16 in Adults with Moderate-to-Severe Atopic Dermatitis Who Do Not Achieve IGA 0/1
https://doi.org/10.1007/s40257-023-00817-0
Documents that mention this clinical trial
Tralokinumab Efficacy and Safety, with or without Topical Corticosteroids, in North American Adults with Moderate-to-Severe Atopic Dermatitis: A Subanalysis of Phase 3 Trials ECZTRA 1, 2, and 3
https://doi.org/10.1007/s13555-022-00805-y
Long-Term Disease Control and Minimal Disease Activity of Head and Neck Atopic Dermatitis in Patients Treated with Tralokinumab up to 4 Years
https://doi.org/10.1007/s40257-025-00931-1
Tralokinumab Efficacy Over 1 Year in Adults with Moderate-to-Severe Atopic Dermatitis: Pooled Data from Two Phase III Trials
https://doi.org/10.1007/s40257-023-00806-3
Tralokinumab Provides Clinically Meaningful Responses at Week 16 in Adults with Moderate-to-Severe Atopic Dermatitis Who Do Not Achieve IGA 0/1
https://doi.org/10.1007/s40257-023-00817-0
Documents that mention this clinical trial
Long-Term Disease Control and Minimal Disease Activity of Head and Neck Atopic Dermatitis in Patients Treated with Tralokinumab up to 4 Years
https://doi.org/10.1007/s40257-025-00931-1
Funding for this research was provided by:
LEO Pharma A/S
Article History
Accepted: 9 February 2025
First Online: 14 March 2025
Declarations
:
: The ECZTRA 1, ECZTRA 2, and ECZTEND trials were sponsored by LEO Pharma A/S (Ballerup, Denmark).
: Raj Chovatiya has served as an advisor, consultant, speaker, and/or investigator for AbbVie, Amgen, AnaptysBio, Apogee Therapeutics, Arcutis, Argenx, Beiersdorf, Boehringer Ingelheim, Bristol Myers Squibb, Cara Therapeutics, CLn Skin Care, Dermavant, Eli Lilly and Company, EMD Serono, FIDE, Formation Bio, Galderma, Genentech, GSK, Johnson & Johnson, Incyte, LEO Pharma, L’Oréal, Nektar Therapeutics, Novartis, Opsidio, Pfizer Inc., RAPT, Regeneron, Sanofi, Sitryx, Takeda, TRex Bio, and UCB. Raj Chovatiya is an Editorial Board member of the American Journal of Clinical Dermatology. He was not involved in the selection of peer reviewers for the manuscript nor any of the subsequent editorial decisions. Simone Ribero received research grants, personal fees, or non-financial support from AbbVie, Almirall, BMS, Galderma, LEO Pharma, Lilly, L’Oreal, Novartis, Pfizer, Pierre Fabre, and Sanofi. Andreas Wollenberg has served as an advisor or paid speaker for, or participated in clinical trials (with honoraria paid to the institution) sponsored by AbbVie, Aileens, Almirall, Amgen, Beiersdorf, Bioderma, Bioproject, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Chugai, DKSH, Eli Lilly, Galapagos, Galderma, Glenmark, GSK, Hans Karrer, Hexal, Janssen-Cilag, Kyowa Kirin, LEO Pharma, L’Oreal, Maruho, MedImmune, MSD, Mylan, MSD, Novartis, Pfizer, Pierre Fabre, Regeneron, Sandoz, Santen, Sanofi-Aventis, and UCB. Chang Ook Park is an investigator for Sanofi, Pfizer, Galderma, Eli Lilly, LEO Pharma, Amgen, AstraZeneca, GSK, Kiniksa Pharmaceuticals, and Teva Pharmaceuticals. Juan Francisco Silvestre has served as an investigator and/or speaker and/or advisor for following pharmaceutical companies: AbbVie, Almirall-Hermal, Amgen, AstraZeneca, Eli-Lilly, Galderma, LEO Pharma, Incyte, Novartis, Pfizer, Regeneron, and Sanofi-Genzyme. H. Chih-ho Hong is a researcher, consultant, and/or advisor for AbbVie, Amgen, Arcutis, Aslan, Bausch Health, Boehringer Ingelheim, Bristol Meyers Squibb, Celgene, Dermavant, Dermira, DS Biopharma, Eli Lilly, Evelo, Galderma, GlaxoSmithKline, Incyte, Janssen, LEO Pharma, MedImmune, Novartis, Pfizer, Regeneron, Roche, Sanofi Genzyme, Sun Pharma, and UCB. Julien Seneschal has served as an investigator, speaker, and/or advisor for Abbvie, Almirall, Eli Lilly, Galderma, Janssen, LEO Pharma, Novartis, Pfizer, and Sanofi‐Genzyme. Hidehisa Saeki received lecture fees and/or clinical research funding and/or grant donations from Mitsubishi Tanabe Pharma Corporation, Taiho Pharmaceutical Co., Ltd., AbbVie GK, Sanofi K.K., Torii Pharmaceutical Co. Ltd., Maruho Co., Ltd., Japan Tobacco Inc., Eli Lilly Japan K.K., LEO Pharma K.K., Otsuka Pharmaceutical Co., Ltd., Novartis Pharma K.K, Pfizer Japan Inc., Amgen Inc., Eisai Co., Ltd., and Tokiwa Pharmaceutical Co., Ltd. Jacob P. Thyssen is an employee of LEO Pharma and holds stock options, and served previously as an advisor for AbbVie, Almirall, Arena Pharmaceuticals, Coloplast, OM Pharma, Aslan Pharmaceuticals, Union Therapeutics, Eli Lilly & Co, Pfizer, Regeneron, and Sanofi-Genzyme; a speaker for AbbVie, Almirall, Eli Lilly & Co, Pfizer, Regeneron, and Sanofi Genzyme; and received research grants from Pfizer, Regeneron, and Sanofi Genzyme. Christian Bjerregård Øland is a former employee of LEO Pharma A/S. Le Gjerum and Douglas Maslin are employees and shareholders of LEO Pharma A/S. Andrew Blauvelt has served as a speaker (received honoraria) for Eli Lilly and Company and UCB, has served as a scientific adviser (received honoraria) for AbbVie, Almirall, Alumis, Amgen, Anaptysbio, Apogee, Arcutis, Boehringer Ingelheim, Bristol Myers Squibb, Dermavant, Eli Lilly and Company, Galderma, GlaxoSmithKline, Incyte, IQVIA, Janssen, LEO Pharma, Lipidio, Merck, Novartis, Oruka, Paragon, Pfizer, Regeneron, Sanofi, Spherix Global Insights, Sun Pharma, Takeda, UCB Pharma, and Union, has acted as a clinical study investigator (institution has received clinical study funds) for AbbVie, Acelyrin, Almirall, Alumis, Amgen, Arcutis, Boehringer Ingelheim, Bristol-Myers Squibb, Dermavant, Eli Lilly and Company, Galderma, Incyte, Janssen, LEO Pharma, Merck, Novartis, Pfizer, Regeneron, Sanofi, Sun Pharma, Takeda, and UCB Pharma, and owns stock in Lipidio and Oruka.
: The ECZTRA 1, ECZTRA 2, and ECZTEND trials were sponsored by LEO Pharma A/S (Ballerup, Denmark) and conducted in accordance with the ethical principles derived from international guidelines including the Declaration of Helsinki and Council for International Organizations of Medical Sciences International Ethical Guidelines and in compliance with International Council for Harmonisation guidelines for Good Clinical Practice. The clinical trials were approved by institutional review boards or ethics committees at each study site. These trials followed the Consolidated Standards of Reporting Trials reporting guideline.
: All patients provided written informed consent.
: Not applicable.
: Data will be made available, upon request to the study sponsor, following review by the external patient and the scientific review board.
: Not applicable.
: Conceptualization: all authors contributed equally; investigation: all authors contributed equally; data curation: CBØ; formal analysis: CBØ (lead); methodology: CBØ (equal), DM (equal); writing: all authors contributed equally; review/editing: all authors contributed equally. All authors read and approved the final version of the manuscript.