Recent Updates
Recently added Catalysts
ICU Positive Sentiment Score: 70/100

SeaStar Medical to Report First Quarter Financial Results on May 14, 2025

Key Takeaway: SeaStar Medical Holding Corporation (Nasdaq: ICU) announced it will report its first quarter financial results on May 14, 2025, following market close. The company also plans to host a webcast and conference call to discuss its financial performance and business progress. SeaStar is recognized for its FDA-approved product QUELIMMUNE, aimed at treating critically ill pediatric patients with acute kidney injury. Additionally, the company's Selective Cytopheretic Device therapy has been designated as a Breakthrough Device for six indications.

Market Sentiment Analysis

POSITIVE FACTORS

  • SeaStar Medical is focused on transforming treatments for critically ill patients.
  • The company achieved FDA approval for its product QUELIMMUNE in 2024.
  • They have received Breakthrough Device Designation for six indications.

Full Press Release Details

DENVER, May 07, 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 first quarter financial results after market close on Wednesday, May 14, 2025, and host a webcast and conference call to discuss its financial results and business progress.
Date/Time: Wednesday, May 14, 2025, at 4:30 p.m. ET / 2:30 p.m. MT
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 May 20, 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 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, 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 Q1 financial results?

SeaStar Medical will report its Q1 financial results on May 14, 2025.

What is SeaStar Medical's first commercial product?

SeaStar Medical's first commercial product is QUELIMMUNE (SCD-PED), approved in 2024.

How can I access the SeaStar Medical conference call?

You can dial 1 (800) 715-9871 within the U.S. for the conference call.

What condition does QUELIMMUNE treat?

QUELIMMUNE treats life-threatening acute kidney injury in critically ill pediatric patients.

What designation has SeaStar's SCD therapy received?

The SCD therapy has been awarded Breakthrough Device Designation by the FDA.

Last updated: May 7, 2025