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SeaStar Medical to Participate in the HC Wainwright 27th Annual Global Investment Conference

Key Takeaway: SeaStar Medical will present at the HC Wainwright 27th Annual Global Investment Conference on September 5, 2025. The company focuses on treatments for critically ill patients, with its QUELIMMUNE therapy being the first FDA-approved product for life-threatening acute kidney injury in pediatric patients. The therapy has received Breakthrough Device Designation for several indications, and a pivotal trial is ongoing for adult patients.
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POSITIVE FACTORS

  • Participation in a major investment conference highlights company visibility.
  • QUELIMMUNE therapy is FDA approved, indicating regulatory confidence.
  • Breakthrough Device Designation for multiple indications suggests innovation.

Full Press Release Details

DENVER, Sept. 04, 2025 (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 its participation in the upcoming HC Wainwright 27thAnnual Global Investment Conference.
The SeaStar Medical presentation can be viewed on Friday, September 5, 2025, at 7:00 am Eastern Time. The presentation can be accessed by visiting theEvents & Presentations page, located under the Investor Relations section of theSeaStar Medical website, and will be available for 60 days following the presentation.

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. TheQUELIMMUNE (SCD-PED)therapy is SeaStar Medical’s first commercial product based on its patented Selective Cytopheretic Device (SCD) technology. It was approved in 2024 by the U.S. Food and Drug Administration (FDA). QUELIMMUNE 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 in critically ill pediatric patients. SeaStar’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 a pivotal trial of its SCD therapy in adult patients with AKI requiring continuous renal replacement therapy (CRRT), a life-threatening condition with no effective treatment options that impacts over 200,000 adults in the US annually.
For more information visitwww.seastarmedical.comor visit us onLinkedInorX.

Frequently Asked Questions

When will SeaStar Medical present at the conference?

SeaStar Medical's presentation is scheduled for September 5, 2025, at 7:00 am ET.

What is QUELIMMUNE?

QUELIMMUNE is SeaStar Medical's FDA-approved therapy for life-threatening acute kidney injury.

What designation has QUELIMMUNE received?

QUELIMMUNE has received Breakthrough Device Designation for multiple therapeutic indications.

What is the focus of SeaStar Medical?

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

Last updated: Sep 4, 2025