Cytokinetics to file FDA sNDA for aficamten in non-obstructive HCM in Q4 2026
CYTK•Phase 3 results support the move
The move follows positive Phase 3 ACACIA-HCM results, meeting dual primary endpoints at 36 weeks on KCCQ-CSS and pVO2.
Planned FDA filing for aficamten
Cytokinetics plans to file a supplemental New Drug Application with the FDA in Q4 2026 for aficamten in symptomatic non-obstructive HCM.



