Regeneron Pharmaceuticals IncFDA Priority Review and EMA acceptance for cemdisiran in generalized myasthenia gravis, with potential to be first siRNA treatment and only subcutaneous option with four-times-a-year dosing.

Regeneron Pharmaceuticals has received FDA acceptance with Priority Review for cemdisiran in generalized myasthenia gravis, and the EMA has also accepted the marketing application, aligning regulatory review on both sides of the Atlantic. Phase 3 trial data for cemdisiran were published in The Lancet, providing peer-reviewed clinical evidence. If approved, cemdisiran would be the first siRNA treatment for generalized myasthenia gravis and the only subcutaneous option with four-times-a-year dosing, potentially addressing an area of significant unmet need among the estimated 85,000 MG patients in the US and broader global prevalence. The FDA's Priority Review sets an action date in November 2026, with a planned Japan filing in early 2027. Regeneron's stock is at $654.27, down 15.7% year to date but up 20.2% over the past year.
Regeneron Pharmaceuticals IncFDA Priority Review and EMA acceptance for cemdisiran in generalized myasthenia gravis, with potential to be first siRNA treatment and only subcutaneous option with four-times-a-year dosing.