Cytokinetics Announces European Commission Approval of MYQORZO® (aficamten) for the Treatment of Adults with Symptomatic Obstructive Hypertrophic Cardiomyopathy
Cytokinetics announced that the European Commission (EC) has approved MYQORZO® (aficamten) for the treatment of symptomatic obstructive hypertrophic cardiomyopathy (oHCM) in adult patients. This approval is based on positive results from the SEQUOIA-HCM clinical trial, demonstrating significant improvements in exercise capacity and symptoms. The company plans its first European launch in Germany in Q2 2026, offering a new treatment option for patients with oHCM.
This page may contain third-party content, which is provided for information purposes only (not representations/warranties) and should not be considered as an endorsement of its views by Gate, nor as financial or professional advice. See Disclaimer for details.
Cytokinetics Announces European Commission Approval of MYQORZO® (aficamten) for the Treatment of Adults with Symptomatic Obstructive Hypertrophic Cardiomyopathy
Cytokinetics announced that the European Commission (EC) has approved MYQORZO® (aficamten) for the treatment of symptomatic obstructive hypertrophic cardiomyopathy (oHCM) in adult patients. This approval is based on positive results from the SEQUOIA-HCM clinical trial, demonstrating significant improvements in exercise capacity and symptoms. The company plans its first European launch in Germany in Q2 2026, offering a new treatment option for patients with oHCM.