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SeaStar Medical Announces CEO Interview on Benzinga All Access to Occur Today at Approximately 10:50 am Eastern Time

Key Takeaway: SeaStar Medical Holding Corporation (Nasdaq: ICU) announced that CEO Eric Schlorff will be a guest on the Benzinga All Access Show today at around 10:50 am Eastern Time. The live broadcast can be accessed via YouTube, and a recorded version will be available on the company's investor relations webpage. SeaStar is recognized for its groundbreaking treatments for critically ill patients, including its recently FDA-approved product for acute kidney injury in pediatric patients.

Market Sentiment Analysis

POSITIVE FACTORS

  • CEO Eric Schlorff's interview highlights SeaStar's innovations.
  • Company's QUELIMMUNE product received FDA approval, addressing a rare condition.
  • Selective Cytopheretic Device therapy has Breakthrough Device Designation.

Full Press Release Details

DENVER, April 30, 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 Eric Schlorff, CEO of SeaStar Medical, will be a featured guest today, Wednesday, April 30th, at approximately 10:50 am Eastern Time on the Benzinga All Access Show.
The event will be broadcast live and can be viewed at https://youtube.com/live/ki1hFktn_2Y?feature=share. An archived recording of the presentation will be available on the investor relations section of the Sea Star Medical’s website on the Events and Presentations page.
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.

Frequently Asked Questions

What event is SeaStar Medical CEO Eric Schlorff attending?

Eric Schlorff will be a featured guest on the Benzinga All Access Show.

What is QUELIMMUNE approved for?

QUELIMMUNE is approved for life-threatening acute kidney injury in critically ill children.

What designation has SeaStar Medical received for its SCD therapy?

SeaStar's SCD therapy has received Breakthrough Device Designation for four indications.

What condition is the pivotal trial targeting?

The trial is targeting acute kidney injury in adults needing continuous renal replacement therapy.

Where can I find the live broadcast of the event?

The event can be viewed live on YouTube at the given link.

Last updated: Apr 30, 2025