Tocilizumab (TCZ; Actemra®; Roche/Genentech in the US; Chugai Pharmaceutical Co. in Japan) is a recombinant, humanized monoclonal antibody directed against the interleukin-6 (IL-6) receptor and currently approved by the Food and Drug Administration (FDA) and the European Commission to treat adults with moderately to severely active rheumatoid arthritis (RA) and pediatric patients with polyarticular Juvenile Idiopathic Arthritis (JIA) or systemic JIA. The FDA has also approved TCZ to treat giant cell (temporal) arteritis and adults and pediatric patients with chimeric antigen receptor (CAR) T cell-induced severe or life-threatening cytokine release syndrome. In Japan, TCZ is approved for the treatment of Castleman's Disease and Takayasu Arteritis. Sarilumab (Kevzara®; Regeneron in the US; Sanofi outside the US) is a similar fully humanized IL-6 R antagonist indicated for the treatment of adults with moderate to severe rheumatoid arthritis (RA). Common side-effects of IL-6 R inhibition include injection site reaction, upper respiratory symptoms, systemic hypertension, hypercholesterolemia, elevated liver enzymes, neutropenia, and thrombocytopenia. Less common complications include severe, opportunistic infections and intestinal perforation. Siltuximab (Sylvant®; EUSA Pharma) is a chimeric monoclonal antibody targeting IL-6 that is approved in both North America and Europe for the treatment of patients with multicentric Castleman's disease who are both human immunodeficiency virus and human herpesvirus-8 negative. Additional monoclonal antibodies targeting IL-6, including sirukumab (Johnson and Johnson/Centocor), olokizumab (R-Pharm), and clazakizumab (Bristol Myers Squib/ Alder Biopharmaceuticals), are advancing through phase 2/3 clinical development, but have yet to receive regulatory approval in North America or Europe. 1,2 Although not approved specifically for the treatment of ocular inflammatory disease or its complications, a number of studies support the use of TCZ to treat active, noninfectious uveitis or scleritis refractory to conventional immunomodulatory therapies, 3-8 most notably scleritis in the setting of rheumatoid arthritis (RA), 9 JIA-associated uveitis, 9-12 and uveitic macular edema. 13-18 Silpa-archa et al 9 reported on the use of intravenous TCZ, 4 to 8 mg/kg monthly, in a mixed cohort of 17 patients with ocular inflammatory disease refractory to conventional immunotherapy, including five subjects with JIA