Efgartigimod delivers rapid relief for hard-to-treat myasthenia gravis
Most patients with generalized myasthenia gravis saw meaningful symptom improvement within four weeks of treatment with efgartigimod.
Most patients with generalized myasthenia gravis saw meaningful symptom improvement within four weeks of treatment with efgartigimod.
Patient-reported breathing symptoms did not reliably match lung function test results, indicating objective testing remains essential in MG.
People with myasthenia gravis had higher rates of cancer both before and after diagnosis compared with matched controls.
Claseprubart produced rapid and meaningful improvements in daily function and muscle strength in MG, with benefits seen as early as week 1.
Many people with myasthenia gravis are diagnosed and treated without antibody blood tests that can help clarify the diagnosis.
FDA approval of inebilizumab gives adults with generalized myasthenia gravis a new treatment designed for long-lasting symptom control.
Patients with ocular myasthenia gravis who undergo thymectomy before generalization are more likely to achieve lasting remission.
Older adults with myasthenia gravis had higher overall death rates than peers without the condition, mainly due to other chronic illnesses.
Two biologically distinct forms of anti-AChR-positive myasthenia gravis (MG) appear to differ by sex, age and immune response.
Mesenchymal stem cells can calm immune system attacks and slow the muscle wasting seen in MG, potentially improving strength and endurance.