FDA approves new treatment for myasthenia gravis

FDA

17 December 2021 - The U.S. Food and Drug Administration today approved Vyvgart (efgartigimod) for the treatment of generalized myasthenia gravis in adults who test positive for the anti-acetylcholine receptor antibody.

The safety and efficacy of Vyvgart were evaluated in a 26-week clinical study of 167 patients with myasthenia gravis who were randomised to receive either Vyvgart or placebo.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US