July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Intravitreal Adalimumab for Noninfectious Uveitis: Clinical Trial Preliminary Data
Author Affiliations & Notes
  • Rola N Hamam
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Rachid Istambouli
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Ahmad M. Mansour
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Maamoun Abdul Fattah
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Carl-Joe Mehanna
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Julien Torbey
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Nasrine Anais El Salloukh
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Haytham I. Salti
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Souha Allam
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Alaa Bou Ghannam
    Ophthalmology, American University of Beirut, Beirut, Lebanon
  • Footnotes
    Commercial Relationships   Rola Hamam, None; Rachid Istambouli, None; Ahmad Mansour, None; Maamoun Abdul Fattah, None; Carl-Joe Mehanna, None; Julien Torbey, None; Nasrine Anais El Salloukh, None; Haytham Salti, None; Souha Allam, None; Alaa Bou Ghannam, None
  • Footnotes
    Support  National Council for Scientific Research (CNRS) 103485
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 3518. doi:
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      Rola N Hamam, Rachid Istambouli, Ahmad M. Mansour, Maamoun Abdul Fattah, Carl-Joe Mehanna, Julien Torbey, Nasrine Anais El Salloukh, Haytham I. Salti, Souha Allam, Alaa Bou Ghannam; Intravitreal Adalimumab for Noninfectious Uveitis: Clinical Trial Preliminary Data. Invest. Ophthalmol. Vis. Sci. 2019;60(9):3518.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Subcutaneous (SC) Adalimumab is FDA-approved for the treatment of noninfectious intermediate, posterior and panuveitis, but poses the risk for serious systemic side effects. To avoid them, intravitreal (IV) administration of this drug offers an interesting alternative, which has not been sufficiently studied to date. This is an open-label randomized clinical trial that aims to compare the efficacy and safety of IV Adalimumab to that of SC Adalimumab.

Methods : 13 patients(25 eyes), out of a total target of 32, with active noninfectious posterior or panuveitis have been enrolled and 9 completed the study so far. Patients are equally randomized to receive SC Adalimumab(80 mg at time 0, then 40 mg on week 1, then 40 mg every other week) or IV injections of the drug(1.5 mg/0.03 mL at time 0, on week 2, then every 4 weeks) for 26 weeks. Full ophthalmologic examination and Fluorescein Angiography (FA) are performed, and Central Retinal Thickness (CRT) is determined by Optical Coherence Tomography for all patients at baseline, weekly for the first 2 weeks, then monthly. Each FA is graded according to a standard scoring system. For the current small sample, baseline, mid- and end-study results of the main outcomes are compared using Mann-Whitney and Fischer’s exact test.

Results : The mean Best Corrected Visual Acuity (BCVA) in the IV group (n=8) at baseline, mid- and end-study was not statistically different from that of the SC group (n=10), as well as the mean gain of ETDRS letters(10 vs 12,p=0.7).There was also no statistically significant difference between the 2 groups in the proportion of patients with anterior chamber or vitreous activity, FA scores, or total decrease in CRT and FA scores(Table 1).CRT was higher at baseline in the SC group(370 ± 33) than in the IV group(261±19, p=0.003), but it became comparable in the 2 arms on further follow-up. 1 patient in the SC group developed a urinary tract infection, and 2 patients developed an upper respiratory tract infection. No adverse events where reported in the IV group.

Conclusions : The preliminary results of our study suggest that IV Adalimumab may be as effective as SC Adalimumab in the treatment of noninfectious uveitis, while potentially sparing its systemic side effects.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

 

Main outcomes (mean±SEM for continuous variables) at baseline, 14 weeks and 26 weeks. ETDRS=Early Treatment Diabetic Retinopathy Study; dBCVA=Total change in BCVA; dCRT=Total change in CRT.

Main outcomes (mean±SEM for continuous variables) at baseline, 14 weeks and 26 weeks. ETDRS=Early Treatment Diabetic Retinopathy Study; dBCVA=Total change in BCVA; dCRT=Total change in CRT.

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