Uveitis Clinical Trial
Official title:
Mycophenolate Sodium (Myfortic®) in the Treatment of Corticosteroid-refractory Autoimmune Uveitis:Pilot Study
This study is designed to explore the use of Myfortic® in patients with steroid-refractory uveitis. The aim of the study will be to show the therapeutic effect of Myfortic® in managing uveitis patients.
This study is a single arm prospective evaluation in which patients with uveitis are treated
with Myfortic® in a dose of 360 mg bid for six months. From day 0, Myfortic will be combined
with 1 mg/kg prednisone. Prednisone will be tapered from week 1 based on the clinical
findings of the ophthalmologist.
There will be no other stratification of patients. After the screening, patients will be
treated with Myfortic® for 6 months. Patients will be seen at month 1, 3, and 6. Thereafter
patients will be followed up at month 12. Efficacy and safety assessments will be performed
at each visit.
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Observational Model: Cohort, Time Perspective: Prospective
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