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SeaStar Medical to Report Third Quarter Financial Results on November 11, 2026

Key Takeaway: SeaStar Medical Holding Corporation (Nasdaq: ICU) will report its third quarter financial results on November 11, 2026. The company focuses on treatments for critically ill patients, with its first product, QUELIMMUNE, approved by the FDA in 2024. SeaStar is also conducting a pivotal trial for its SCD therapy in adult patients with acute kidney injury.

Market Sentiment Analysis

POSITIVE FACTORS

  • Company will report Q3 financial results soon.
  • QUELIMMUNE is the only FDA approved treatment for AKI.
  • SCD therapy has Breakthrough Device Designation for seven indications.
  • Company is conducting a pivotal clinical trial for AKI.

Full Press Release Details

DENVER, Nov. 04, 2026 (GLOBE NEWSWIRE) -- SeaStar Medical Holding Corporation (Nasdaq: ICU), a commercial-stage healthcare company focused on transformational treatments for critically ill patients facing organ failure and potential loss of life, announced today that it will report its third quarter financial results after market close on Wednesday, November 11, 2026, and host a webcast and conference call to discuss its financial results and business progress.
Date/Time: Wednesday, November 11, 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 transformational 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 in critically ill pediatric patients. SeaStar Medical’s Selective Cytopheretic Device (SCD) therapy has been awarded Breakthrough Device Designation for seven 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: IR@SeaStarMed.com

Frequently Asked Questions

When will SeaStar Medical report its Q3 results?

SeaStar Medical will report its Q3 financial results on November 11, 2026.

What is QUELIMMUNE?

QUELIMMUNE is the only FDA approved treatment for life-threatening acute kidney injury.

What is the focus of SeaStar Medical?

SeaStar Medical focuses on treatments for critically ill patients facing organ failure.

What trial is SeaStar Medical currently conducting?

The company is conducting the NEUTRALIZE-AKI pivotal clinical trial for SCD therapy.

Last updated: Nov 4, 2026