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SeaStar Medical to Report Fourth Quarter and Year-End 2024 Financial Results on March 27, 2025

Key Takeaway: SeaStar Medical Holding Corporation (Nasdaq: ICU) has announced it will report its fourth quarter and year-end 2024 financial results on March 27, 2025. The company is focused on treatment options for critically ill patients and has achieved FDA approval for its product QUELIMMUNE, targeting a rare condition. A pivotal trial for its Selective Cytopheretic Device therapy in adult patients is ongoing, addressing a significant healthcare need.

Market Sentiment Analysis

POSITIVE FACTORS

  • Company is reporting financial results, indicating transparency and accountability.
  • First product, QUELIMMUNE, is FDA approved, showcasing successful innovation.
  • Breakthrough Device Designation for SCD therapy presents potential for expedited approvals.

Full Press Release Details

DENVER, March 24, 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 that it will report its fourth quarter and year-end 2024 financial results after market close on Thursday, March 27, 2025, and host a webcast and conference call to discuss its financial results and business progress.
Date/Time: Thursday, March 27, at 4:30 p.m. ET / 1:30 p.m. PT
Webcast: The live webcast and replay can be found here .
Conference ID: 2078693
Dial-in numbers: 1 (800) 715-9871 within the U.S.
1 (646) 307-1963 from outside the U.S.
A replay of the call will be available after 7:30 pm ET and can be accessed as follows:
The webcast replay is available here.
The call replay number is 1 (609) 800-9909 and will be available through April 3, 2025.
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’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 in critically ill pediatric patients. SeaStar’s Selective Cytopheretic Device (SCD) therapy has been awarded Breakthrough Device Designation for four 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, 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.
SeaStar Investor Relations:

Frequently Asked Questions

When will SeaStar Medical report its Q4 and year-end 2024 results?

SeaStar Medical will report its financial results on March 27, 2025.

What product did SeaStar Medical launch in 2024?

SeaStar launched QUELIMMUNE (SCD-PED), approved for acute kidney injury.

How can I access the SeaStar Medical conference call?

Dial 1 (800) 715-9871 in the U.S. or 1 (646) 307-1963 internationally.

What is the focus of SeaStar Medical's work?

SeaStar Medical is dedicated to treating critically ill patients facing organ failure.

What designation has the SCD therapy received from the FDA?

The SCD therapy has received Breakthrough Device Designation for four conditions.

Last updated: Mar 24, 2025