Regeneron Pharmaceuticals IncFDA and EMA accepted regulatory filings for cemdisiran, a potential first-in-class siRNA for gMG, with Priority Review and positive trial data.

Regeneron Pharmaceuticals announced that both the FDA and EMA have accepted regulatory submissions for cemdisiran to treat adult patients with generalized myasthenia gravis who are anti-acetylcholine receptor antibody-positive. The FDA accepted the New Drug Application under Priority Review with a target action date in November 2026, while a European Commission decision is anticipated in the second half of 2027. Cemdisiran could be the first siRNA approved for gMG and the only therapy offered subcutaneously with four times a year dosing. The submissions are supported by data from the Phase 3 NIMBLE trial, one of the largest global interventional gMG trials conducted to date, with full results published in The Lancet and presented at the American Academy of Neurology Annual Meeting in April 2026. A regulatory filing in Japan is planned for early 2027.
Regeneron Pharmaceuticals IncFDA and EMA accepted regulatory filings for cemdisiran, a potential first-in-class siRNA for gMG, with Priority Review and positive trial data.