Abstract
BACKGROUND: Adalimumab has demonstrated efficacy in non-infectious uveitis. With the introduction of biosimilar agents such as Amgevita, we aimed to quantify efficacy and tolerability compared to Humira in a multi-centre UK cohort.
METHODS: Patients identified from tertiary uveitis clinics in 3 centres, after institution-mandated switching was implemented.
RESULTS: Data collected for 102 patients, aged 2-75 years, with 185 active eyes. Following switch, rates of uveitis flare were not significantly different (13 events before, 21 after, p = .132). Rates of elevated intraocular pressure were decreased (32 before, 25 afterwards, p = .006) and dosing of oral and intra-ocular steroids was stable. Twenty-four patients (24%) requested to return to Humira, commonly due to pain from injection or technical difficulty with the device.
CONCLUSION: Amgevita is safe and effective for inflammatory uveitis with non-inferiority to Humira. Significant numbers of patients requested to switch back due to side effects including injection site reactions.
Original language | English |
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Pages (from-to) | 442-446 |
Number of pages | 5 |
Journal | Ocular Immunology and Inflammation |
Volume | 32 |
Issue number | 4 |
Early online date | 21 Feb 2024 |
DOIs | |
Publication status | Published - 20 Apr 2024 |
Bibliographical note
Publisher Copyright:© 2023 The Author(s). Published with license by Taylor & Francis Group, LLC.
Keywords
- Humans
- Adalimumab/therapeutic use
- Uveitis/drug therapy
- Middle Aged
- Female
- Male
- Adult
- Biosimilar Pharmaceuticals/therapeutic use
- Adolescent
- Aged
- Child
- Child, Preschool
- Young Adult
- Treatment Outcome
- Retrospective Studies
- Anti-Inflammatory Agents/therapeutic use
- Drug Substitution