Press Releases May 12, 2026 04:00 PM

Cytokinetics to Participate in the 2026 RBC Capital Markets Global Healthcare Conference

Cytokinetics to present at RBC Capital Markets Global Healthcare Conference amidst ongoing cardiac drug development

By Leila Farooq CYTK

Cytokinetics announced participation in a fireside chat at the 2026 RBC Capital Markets Global Healthcare Conference. The company highlighted progress on its cardiac drug candidates, including the approved MYQORZO® (aficamten) for obstructive hypertrophic cardiomyopathy and positive Phase 3 results for aficamten in non-obstructive HCM. They continue to develop investigational cardiac myosin activators and inhibitors for heart failure treatments, with upcoming presentations and regulatory discussions planned.

Cytokinetics to Participate in the 2026 RBC Capital Markets Global Healthcare Conference
CYTK

Key Points

  • Cytokinetics management will present at a major healthcare investor conference, providing updates on pipeline and strategy.
  • MYQORZO (aficamten) is approved in key markets for obstructive hypertrophic cardiomyopathy, representing a commercial milestone.
  • Positive topline Phase 3 data for aficamten in non-obstructive HCM positions the company for regulatory discussions and potential label expansion.
  • Ongoing development of cardiac myosin activators and inhibitors targets significant unmet needs in heart failure treatment, impacting biopharma and cardiovascular therapy sectors.

SOUTH SAN FRANCISCO, Calif., May 12, 2026 (GLOBE NEWSWIRE) -- Cytokinetics, Incorporated (Nasdaq: CYTK) today announced that members of the Company management team will participate in a fireside chat at the 2026 RBC Capital Markets Global Healthcare Conference on Tuesday, May 19, 2026 at 3:35 PM Eastern Time in New York, NY.

Interested parties may access the live webcast of the fireside chat by visiting the Investors & Media section of the Cytokinetics website at https://ir.cytokinetics.com/. The webcast replays will be archived on the Cytokinetics website for 90 days following the conclusion of the event.

About Cytokinetics

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction. Cytokinetics’ MYQORZO® (aficamten) is a cardiac myosin inhibitor approved in the U.S., Europe and China for the treatment of adults with symptomatic obstructive hypertrophic cardiomyopathy (oHCM). Following positive topline results in ACACIA-HCM, a Phase 3 clinical trial of aficamten in patients with non-obstructive HCM (nHCM), the company is preparing to present the full results at an upcoming medical meeting and discuss them with the U.S. FDA and other regulatory authorities. Cytokinetics is also developing omecamtiv mecarbil, an investigational cardiac myosin activator for the potential treatment of patients with heart failure with severely reduced ejection fraction and ulacamten, an investigational cardiac myosin inhibitor for the potential treatment of heart failure with preserved ejection fraction, while continuing pre-clinical research and development in muscle biology.

For additional information about Cytokinetics, visit www.cytokinetics.com and follow us on X, LinkedIn, Facebook and YouTube.

Disclaimer 

Omecamtiv mecarbil and ulacamten are investigational medicines. They have not been approved nor determined to be safe or efficacious for any disease state or any indication by FDA or any other regulatory agency.

Forward-Looking Statements

This press release contains forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995 (the “Act”). Cytokinetics disclaims any intent or obligation to update these forward-looking statements and claims the protection of the Act’s Safe Harbor for forward-looking statements. Examples of such statements include, but are not limited to, statements relating to Cytokinetics’ and its partners’ research and development activities of Cytokinetics’ product candidates. Such statements are based on management’s current expectations, but actual results may differ materially due to various risks and uncertainties, including, but not limited to the risks related to Cytokinetics’ business outlines in Cytokinetics’ filings with the Securities and Exchange Commission. Forward-looking statements are not guarantees of future performance, and Cytokinetics’ actual results of operations, financial condition and liquidity, and the development of the industry in which it operates, may differ materially from the forward-looking statements contained in this press release. Any forward-looking statements that Cytokinetics makes in this press release speak only as of the date of this press release. Cytokinetics assumes no obligation to update its forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.

CYTOKINETICS® and the CYTOKINETICS C-shaped logo are registered trademarks of Cytokinetics in the U.S. and certain other countries.

MYQORZO® is a registered trademark of Cytokinetics in the U.S. and European Union.

Contact:
Cytokinetics
Diane Weiser
Senior Vice President, Corporate Affairs
(415) 290-7757


Risks

  • Investigational products like omecamtiv mecarbil and ulacamten have not been approved and carry uncertainty around safety and efficacy outcomes.
  • Regulatory approval processes and outcomes remain uncertain and could impact the company's commercial prospects.
  • Clinical development risks including potential unexpected trial results or delays could affect pipeline value and investor confidence.

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