Abstract
This case report details the first use of ravulizumab in Chile for a patient with acetylcholine receptor (AChR)-positive myasthenia gravis (MG) who did not respond to rituximab (RTX). A 26-year-old female presented with progressive MG symptoms, including fatigue and bilateral ptosis. Despite conventional treatment and thymectomy, she experienced multiple myasthenic crises. Following the lack of response to RTX, ravulizumab was initiated, resulting in a significant improvement in the Myasthenia Gravis Activities of Daily Living (MG-ADL) score in less than two weeks. Ravulizumab, a monoclonal antibody that inhibits complement component C5, was approved for MG in 2022 and is being assessed for efficacy in neurological disorders. This report highlights its potential as a therapy for MG in the absence of robust local evidence, offering a novel therapeutic option for managing this debilitating condition.