News

Nipocalimab up for approval for gMG in the European Union

Johnson & Johnson has submitted an application to the European Medicines Agency (EMA) seeking approval of nipocalimab to treat people with generalized myasthenia gravis (gMG). The request includes gMG patients who are positive for MG-causing autoantibodies targeting acetylcholine receptors (AChRs), muscle-specific tyrosine (MuSK), and low-density lipoprotein…

Soliris, Vyvgart effective in adults with generalized MG: Study

Both Soliris (eculizumab) and Vyvgart (efgartigimod alfa-fcab) rapidly eased disease severity among adults with generalized myasthenia gravis (gMG), according to a real-world study that compared the two therapies. Soliris outperformed Vyvgart in its ability to reduce gMG severity and corticosteroid dose over a year of treatment, however.

Novel system may predict outcomes in MG linked to thymus tumor

Using a combination of two standardized assessment tools may be better than the classification process now in place in predicting the outcomes of people with a thymoma, or thymus tumor, associated with myasthenia gravis (MG), a new study suggests. The newly proposed system, from researchers in China, would classify…

Nipocalimab up for approval for gMG in the US

Johnson & Johnson has submitted an application to the U.S. Food and Drug Administration (FDA) seeking approval of nipocalimab to treat people with generalized myasthenia gravis (gMG). The application covers gMG patients who are positive for disease-causing antibodies against acetylcholine receptors (AChRs), muscle-specific kinase (MuSK), and low…