Press Releases May 6, 2026 08:20 AM

SeaStar Medical to Report First Quarter Financial Results on May 13, 2026

SeaStar Medical announces Q1 2026 financial results date and webcast for investor update

By Sofia Navarro ICU

SeaStar Medical Holding Corporation, a commercial-stage healthcare company specializing in treatments for critically ill patients with organ failure, will release its Q1 2026 financial results on May 13, 2026. The company will also host a webcast and conference call to discuss business progress and financial performance. SeaStar's flagship product, QUELIMMUNE, is FDA-approved for a rare pediatric kidney injury condition, and its Selective Cytopheretic Device (SCD) therapy is in pivotal trials for adult acute kidney injury.

SeaStar Medical to Report First Quarter Financial Results on May 13, 2026
ICU

Key Points

  • SeaStar Medical will report Q1 2026 financial results on May 13, followed by a webcast and conference call for investors.
  • QUELIMMUNE (SCD-PED) is FDA-approved for treating life-threatening acute kidney injury in pediatric patients due to sepsis.
  • The company is conducting pivotal clinical trials for its SCD therapy targeting adult AKI patients, a critical unmet medical need affecting over 200,000 adults annually in the U.S.

DENVER, May 06, 2026 (GLOBE NEWSWIRE) -- SeaStar Medical Holding Corporation (Nasdaq: ICU), a commercial-stage healthcare company focused on transforming treatments for critically ill patients facing organ failure and potential loss of life, announced today that it will report its first quarter financial results after market close on Wednesday, May 13, 2026, and host a webcast and conference call to discuss its financial results and business progress.

Date/Time:Wednesday, May 13, 2026, at 4:30 p.m. ET / 2:30 p.m. MT Webcast:The live webcast and replay can be found here. Register for the call:Preregistration is required to attend the live call and can be accessed here. A pin code and dial in number will be provided with registration. 

A replay of the call will be available after 7:30 p.m. ET and can be accessed here.

About SeaStar Medical

SeaStar Medical is a commercial-stage healthcare company focused on transforming treatments for critically ill patients facing organ failure and potential loss of life. SeaStar Medical’s first commercial product, QUELIMMUNE (SCD-PED), was approved in 2024 by the U.S. Food and Drug Administration (FDA). It is the only FDA approved product for the ultra-rare condition of life-threatening Acute Kidney Injury (AKI) due to sepsis or a septic condition requiring renal replacement therapy (RRT) in critically ill pediatric patients. SeaStar Medical’s Selective Cytopheretic Device (SCD) therapy has been awarded Breakthrough Device Designation for six therapeutic indications by the FDA, enabling the potential for a speedier pathway to approval and preferable reimbursement dynamics at commercial launch. The company is currently conducting the NEUTRALIZE-AKI pivotal clinical trial of its SCD therapy in adult patients with AKI requiring continuous renal replacement therapy, a life-threatening condition with no effective treatment options that impacts over 200,000 adults in the U.S. annually.

For more information visit www.seastarmedical.com or visit us on LinkedIn or X.

Contact:
SeaStar Investor Relations:
[email protected]


Risks

  • Clinical trial outcomes for the NEUTRALIZE-AKI pivotal trial in adults are uncertain and could impact regulatory approval and commercial potential.
  • Dependence on regulatory approvals for the SCD therapy and potential reimbursement dynamics could influence future revenue streams.
  • Market adoption of new therapies for acute kidney injury involves competition and requires healthcare provider acceptance, posing commercialization risks.

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