2018
DOI: 10.1080/09273948.2018.1491605
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Adalimumab in Active and Inactive, Non-Infectious Uveitis: Global Results from the VISUAL I and VISUAL II Trials

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Cited by 23 publications
(19 citation statements)
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“…The VISUAL study demonstrated the ability of adalimumab to reduce the risk of recurrent uveitis and vision loss in patients with both active (VISUAL I) and inactive disease (VISUAL II). In both mentioned studies, adalimumab offered significantly better improvement than placebo with fairly comparable risk levels, only slightly higher in adalimumab group (2). The observed adverse effects included susceptibility to infections (reactivation of tuberculosis, histoplasmosis, hepatitis B, and fungal infection), hypersensitivity reactions, demyelinating disease, lupus-like syndrome, malignancy, thromboembolic events, and congestive heart failure (3,7).…”
Section: Discussionmentioning
confidence: 94%
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“…The VISUAL study demonstrated the ability of adalimumab to reduce the risk of recurrent uveitis and vision loss in patients with both active (VISUAL I) and inactive disease (VISUAL II). In both mentioned studies, adalimumab offered significantly better improvement than placebo with fairly comparable risk levels, only slightly higher in adalimumab group (2). The observed adverse effects included susceptibility to infections (reactivation of tuberculosis, histoplasmosis, hepatitis B, and fungal infection), hypersensitivity reactions, demyelinating disease, lupus-like syndrome, malignancy, thromboembolic events, and congestive heart failure (3,7).…”
Section: Discussionmentioning
confidence: 94%
“…Adalimumab is a recombinant human IgG1 monoclonal antibody targeting the TNF-α. TNF-α is believed to play a crucial role in pathogenesis of non-infectious uveitis, as it both induces and maintains the inflammation in autoimmune response (2,3,5). Whilst adalimumab has well documented efficacy in reducing signs and symptoms of joint involvement in rheumatoid conditions, it also has an effect on ocular involvement, with an additional advantage of subcutaneous dosing (SQ) over other available biological agents which require intravenous injections (2,3,6,7).…”
Section: Discussionmentioning
confidence: 99%
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