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SeaStar Medical to Report Fourth Quarter and Year-End 2025 Financial Results on March 25, 2026

Key Takeaway: SeaStar Medical Holding Corporation will report its fourth quarter and year-end 2025 financial results on March 25, 2026. The company, which focuses on treatments for critically ill patients, has an FDA-approved product for life-threatening Acute Kidney Injury. Additionally, its Selective Cytopheretic Device therapy has received Breakthrough Device Designation for several indications, and a pivotal clinical trial is currently underway.

Market Sentiment Analysis

POSITIVE FACTORS

  • SeaStar Medical is reporting financial results, indicating business activity.
  • The company has an FDA-approved product for a critical condition.
  • SCD therapy has received Breakthrough Device Designation for multiple indications.
  • The ongoing pivotal clinical trial could lead to significant advancements in treatment.

Full Press Release Details

DENVER, March 18, 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 fourth quarter and year-end 2025 financial results after market close on Wednesday, March 25, 2026, and host a webcast and conference call to discuss its financial results and business progress.
Date/Time: Wednesday, March 25, 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 financial results?

SeaStar Medical will report its fourth quarter and year-end 2025 financial results on March 25, 2026.

What is SeaStar Medical's main focus?

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

What is QUELIMMUNE?

QUELIMMUNE is SeaStar Medical's FDA-approved product for life-threatening Acute Kidney Injury.

What designation has SeaStar's SCD therapy received?

SeaStar's Selective Cytopheretic Device therapy has received Breakthrough Device Designation from the FDA.

What trial is SeaStar currently conducting?

SeaStar is conducting the NEUTRALIZE-AKI pivotal clinical trial for its SCD therapy in adults.

Last updated: Mar 18, 2026