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Cytokinetics Reports Third Quarter 2026 Financial Results and Provides Business Update

Globe Newswire•04/11/2026•16:00 ET
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Key Highlights

  • ➤MYQORZO net product revenue reached $44.5 million in Q3 2026
  • ➤Total Q3 revenue rose to $47.6 million from $1.9 million
  • ➤Q3 net loss narrowed to $190.1 million, or $(1.37) per share
  • ➤Supplemental NDA submission for nHCM expected in Q4 2026
  • ➤Cash, cash equivalents and investments totaled approximately $1.6 billion

Expert Statements

Robert I. Blum, President and Chief Executive Officer of Cytokinetics

“Our third quarter results demonstrate continued strong execution as Cytokinetics enters its next phase of growth as a global specialty cardiology biopharmaceutical company. In the U.S., the launch of MYQORZO continued to build solid momentum and increased velocity with growing adoption across a broadening base of prescribers. Internationally, we continued to expand access to MYQORZO to bring this important medicine to more patients around the world. Now, with our having presented and published the primary results from ACACIA-HCM, the first positive Phase 3 clinical trial in nHCM, we believe aficamten has the potential to become the first and only cardiac myosin inhibitor approved across the full spectrum of HCM. Building on these key results, we are moving swiftly to seek regulatory approvals in both the U.S. and Europe, important next steps toward achieving our Vision 2030.”

Expect to Submit Supplemental NDA for Aficamten in Non-Obstructive HCM in Q4 2026 and Type II Variation in the European Union in Early 2027

~$1.6 Billion in Cash, Cash Equivalents and Investments as of September 30, 2026

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