Cytokinetics reports positive ACACIA-HCM results for aficamten in non-obstructive HCM
The Phase 3 trial hit both primary endpoints, and Cytokinetics plans an FDA supplemental filing in the fourth quarter of 2026.
SEC filing
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The Phase 3 trial hit both primary endpoints, and Cytokinetics plans an FDA supplemental filing in the fourth quarter of 2026.
SEC filing
The company plans a supplemental NDA for aficamten in non-obstructive HCM in the fourth quarter of 2026 after positive Phase 3 topline data.
SEC filing
The company cited new drug approvals and an expanded pipeline as it lifted its full-year Portfolio Receipts outlook to $3,400 million to $3,500 million.
SEC filing