Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, Italy

Adalimumab (ADA), a monoclonal antibody targeting TNF-α, is effective in treating moderate to severe psoriasis. The emergence of biosimilars, such as GP2017 (Hyrimoz®), has raised concerns about their safety and efficacy compared to the originator. This two-year observational study evaluated the ef...

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Main Authors: Marco May Lee, Vito Di Lernia, Francesca Peccerillo, Federico Bardazzi, Michela Tabanelli, Michela Ricci, Davide Melandri, Monica Corazza, Francesca Satolli, Andrea Conti
Format: Article
Language:English
Published: PAGEPress Publications 2025-07-01
Series:Dermatology Reports
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Online Access:https://www.pagepress.org/journals/dr/article/view/10315
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author Marco May Lee
Vito Di Lernia
Francesca Peccerillo
Federico Bardazzi
Michela Tabanelli
Michela Ricci
Davide Melandri
Monica Corazza
Francesca Satolli
Andrea Conti
author_facet Marco May Lee
Vito Di Lernia
Francesca Peccerillo
Federico Bardazzi
Michela Tabanelli
Michela Ricci
Davide Melandri
Monica Corazza
Francesca Satolli
Andrea Conti
author_sort Marco May Lee
collection DOAJ
description Adalimumab (ADA), a monoclonal antibody targeting TNF-α, is effective in treating moderate to severe psoriasis. The emergence of biosimilars, such as GP2017 (Hyrimoz®), has raised concerns about their safety and efficacy compared to the originator. This two-year observational study evaluated the effectiveness and safety of GP2017 in 171 patients from Emilia-Romagna, Italy. Patients were divided into two groups: 78 transitioned from the ADA originator, and 93 were biologic-naive. Changes in the Psoriasis Area and Severity Index (PASI) were analyzed. In the switch group, PASI scores remained stable, while the naive group achieved significant improvements (PASI 75: 52% at 3 months, 89% at 6 months). Adverse events leading to discontinuation were rare. The findings confirm that GP2017 is as effective and safe as the ADA originator, supporting its use as a cost-effective alternative in the treatment of psoriasis. Biosimilars play a crucial role in promoting equitable access to biologic therapies.
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language English
publishDate 2025-07-01
publisher PAGEPress Publications
record_format Article
series Dermatology Reports
spelling doaj-art-33d3ab9bface48f8a86b3ccf6fa0fc372025-08-20T03:17:40ZengPAGEPress PublicationsDermatology Reports2036-73922036-74062025-07-0110.4081/dr.2025.10315Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, ItalyMarco May Lee0Vito Di Lernia1Francesca Peccerillo2Federico Bardazzi3Michela Tabanelli4Michela Ricci5Davide Melandri6Monica Corazza7Francesca Satolli8Andrea Conti9Private Practice, Dermatology, PaduaDermatologic Unit, Arcispedale Santa Maria Nuova, AUSL-IRCCS Reggio EmiliaDermatologic Unit, Arcispedale Santa Maria Nuova, AUSL-IRCCS Reggio EmiliaDermatologic Unit, IRCCS University Hospital of BolognaDermatologic Unit, AUSL Romagna, RavennaDermatologic Unit, AUSL Romagna, ForlìDermatologic Unit and Burn Center, AUSL Romagna, Bufalini Hospital, CesenaSection of Dermatology and Infectious Diseases, Department of Medical Sciences, University of FerraraSection of Dermatology, Department of Clinical and Experimental Medicine, University of ParmaDermatologic Unit, Department of Surgery, Infermi Hospital, AUSL Romagna, Rimini Adalimumab (ADA), a monoclonal antibody targeting TNF-α, is effective in treating moderate to severe psoriasis. The emergence of biosimilars, such as GP2017 (Hyrimoz®), has raised concerns about their safety and efficacy compared to the originator. This two-year observational study evaluated the effectiveness and safety of GP2017 in 171 patients from Emilia-Romagna, Italy. Patients were divided into two groups: 78 transitioned from the ADA originator, and 93 were biologic-naive. Changes in the Psoriasis Area and Severity Index (PASI) were analyzed. In the switch group, PASI scores remained stable, while the naive group achieved significant improvements (PASI 75: 52% at 3 months, 89% at 6 months). Adverse events leading to discontinuation were rare. The findings confirm that GP2017 is as effective and safe as the ADA originator, supporting its use as a cost-effective alternative in the treatment of psoriasis. Biosimilars play a crucial role in promoting equitable access to biologic therapies. https://www.pagepress.org/journals/dr/article/view/10315Psoriasisadalimumabbiosimilarsefficacysafety
spellingShingle Marco May Lee
Vito Di Lernia
Francesca Peccerillo
Federico Bardazzi
Michela Tabanelli
Michela Ricci
Davide Melandri
Monica Corazza
Francesca Satolli
Andrea Conti
Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, Italy
Dermatology Reports
Psoriasis
adalimumab
biosimilars
efficacy
safety
title Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, Italy
title_full Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, Italy
title_fullStr Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, Italy
title_full_unstemmed Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, Italy
title_short Efficacy and safety of adalimumab biosimilar GP2017 in a 24-month treatment period for plaque psoriasis: real-life experience from Emilia-Romagna centers, Italy
title_sort efficacy and safety of adalimumab biosimilar gp2017 in a 24 month treatment period for plaque psoriasis real life experience from emilia romagna centers italy
topic Psoriasis
adalimumab
biosimilars
efficacy
safety
url https://www.pagepress.org/journals/dr/article/view/10315
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