Regeneron Pharmaceuticals IncFDA grants Priority Review for cemdisiran, a potential first-in-class siRNA therapy for gMG, with a target action date in November 2026.

Regeneron Pharmaceuticals announced that the U.S. FDA and EMA have accepted regulatory applications for cemdisiran to treat adult anti-AChR antibody-positive generalized myasthenia gravis, with the FDA granting Priority Review and setting a target action date in November 2026. If approved, cemdisiran would be the first siRNA therapy for gMG and the only treatment administered subcutaneously just four times a year, potentially improving convenience for patients with this rare autoimmune disease. The filing extends Regeneron's complement and RNAi ambitions and adds another potential rare-disease asset to a portfolio already supported by Dupixent, EYLEA HD, and emerging oncology programs. While the Priority Review and quarterly dosing profile may reinforce the depth of the pipeline, market reaction suggests investors remain more focused on near-term growth drivers such as Dupixent indication expansions, EYLEA HD execution, and oncology launches like linvoseltamab.
Regeneron Pharmaceuticals IncFDA grants Priority Review for cemdisiran, a potential first-in-class siRNA therapy for gMG, with a target action date in November 2026.