argenx N.V. is having to take a gradual approach to growing Vyvgart sales as the generalized myasthenia gravis (gMG) product faces hurdles from the COVID-19 pandemic and the lack of medical education on the drug’s target, FcRn.
The US Food and Drug Administration gave Vyvgart (efgartigimod alfa-fcab) the green light on 17 December on the back of data from the Phase III ADAPT trial
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