Recent Updates
Recently added Catalysts
ICU Positive Sentiment

SeaStar Medical to Report Second Quarter Financial Results on August 12, 2026

Key Takeaway: SeaStar Medical Holding Corporation will report its second quarter financial results on August 12, 2026. The company is known for its innovative treatments for critically ill patients, including its FDA-approved product QUELIMMUNE for Acute Kidney Injury. Additionally, they are advancing their Selective Cytopheretic Device therapy through a pivotal clinical trial for adult patients.

Market Sentiment Analysis

POSITIVE FACTORS

  • SeaStar Medical is focused on transformational treatments for critically ill patients.
  • The company has an FDA-approved product for a rare condition affecting pediatric patients.
  • They are conducting a pivotal clinical trial for a therapy addressing a significant unmet need.

Full Press Release Details

DENVER, Aug. 06, 2026 (GLOBE NEWSWIRE) -- SeaStar Medical Holding Corporation (Nasdaq: ICU), a commercial-stage healthcare company focused on transformational treatments for critically ill patients facing organ failure and potential loss of life, announced today that it will report its second quarter financial results after market close on Wednesday, August 12, 2026, and host a webcast and conference call to discuss its financial results and business progress.
Date/Time: Wednesday, August 12, 2026, at 4:30 p.m. ET / 2:30 p.m. MT
Webcast: The live webcast and replay can be found here.
Register for the call: Preregistration is required to attend the live call and can be accessed here. 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 accessed here.

About SeaStar Medical

SeaStar Medical is a commercial-stage healthcare company focused on transformational 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 visit www.seastarmedical.com or visit us on LinkedIn or X.

Contact: SeaStar Investor Relations: IR@SeaStarMed.com

Frequently Asked Questions

When will SeaStar Medical report its Q2 financial results?

SeaStar Medical will report its second quarter financial results on August 12, 2026.

What is SeaStar Medical's focus area?

SeaStar Medical focuses on transformational 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 in pediatric patients.

What clinical trial is SeaStar Medical conducting?

SeaStar Medical is conducting the NEUTRALIZE-AKI pivotal clinical trial for adult patients with Acute Kidney Injury.

Last updated: Aug 6, 2026