With a US filing for efgartigimod imminent, Belgian biotech argenx N.V. has presented more positive data on the potential first-in-class product which has been touted as a future standard of care for the rare autoimmune disease myasthenia gravis.
Additional data from the previously reported Phase III ADAPT trial which enrolled patients who were either acetylcholine receptor-antibody (AChR-A) positive or negative have been presented at the Myasthenia Gravis Foundation of America scientific session, showing impressive responder rates for efgartigimod on two measures of efficacy, the myasthenia gravis activities of daily living (MG-ADL) and quantitative myasthenia gravis (QMG) scores