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

Key Takeaway: SeaStar Medical Holding Corporation will report its first quarter financial results on May 13, 2026. The company is known for its innovative treatments for critically ill patients, particularly those facing organ failure. Its first product, QUELIMMUNE, is FDA-approved for a rare condition in pediatric patients, and it is currently conducting a pivotal trial for adult patients with Acute Kidney Injury.

Market Sentiment Analysis

POSITIVE FACTORS

  • SeaStar Medical is focused on transforming treatments for critically ill patients.
  • The company has an FDA-approved product for life-threatening Acute Kidney Injury.
  • Breakthrough Device Designation awarded for multiple therapeutic indications.

Full Press Release Details

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 foundhere.
Register for the call: Preregistration is required to attend the live call and can be accessedhere. 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 accessedhere.

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 visitwww.seastarmedical.comor visit us onLinkedInorX.

Contact:SeaStar Investor Relations:IR@SeaStarMed.com

Frequently Asked Questions

When will SeaStar Medical report its Q1 financial results?

SeaStar Medical will report its first quarter financial results on May 13, 2026.

What is SeaStar Medical's first commercial product?

SeaStar Medical's first commercial product is QUELIMMUNE, approved for Acute Kidney Injury.

What condition does QUELIMMUNE treat?

QUELIMMUNE treats life-threatening Acute Kidney Injury due to sepsis in pediatric patients.

What trial is SeaStar Medical currently conducting?

The company is conducting the NEUTRALIZE-AKI pivotal clinical trial for adult patients with AKI.

Last updated: May 6, 2026