Alnylam Pharmaceuticals IncCemdisiran accepted for FDA and EMA review for myasthenia gravis, a key regulatory milestone.
U.S. and European regulators have accepted marketing applications for cemdisiran, an experimental myasthenia gravis therapy from Regeneron and Alnylam Pharmaceuticals. The FDA granted priority review with a target action date in November, while the European Medicines Agency accepted a marketing authorization application with final European Commission approval expected in the second half of 2027. The submissions seek approval for the injectable to treat adults with generalized myasthenia gravis who are positive for anti-acetylcholine receptor antibodies, supported by the Phase 3 NIMBLE trial. A regulatory filing in Japan is expected in early 2027.
Alnylam Pharmaceuticals IncCemdisiran accepted for FDA and EMA review for myasthenia gravis, a key regulatory milestone.
Regeneron Pharmaceuticals IncCemdisiran accepted for FDA and EMA review for myasthenia gravis, a key regulatory milestone.