Press Releases August 6, 2026 08:35 AM

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

SeaStar Medical to announce Q2 2026 financial results and host a webcast on August 12, 2026

By Avery Klein
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ICU

SeaStar Medical Holding Corporation, a healthcare company specializing in treatments for critically ill patients with organ failure, will report its second quarter financial results on August 12, 2026. The company will also hold a webcast and conference call to discuss its financial and business progress. SeaStar Medical's flagship product QUELIMMUNE, approved in 2024, targets pediatric acute kidney injury due to sepsis, and its SCD therapy is under pivotal clinical trial for adult acute kidney injury.

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

  • SeaStar Medical reports Q2 2026 results on August 12 with an accompanying webcast and call for investors.
  • The company’s FDA-approved QUELIMMUNE targets ultra-rare pediatric acute kidney injury due to sepsis, marking a significant commercial product.
  • SCD therapy has FDA Breakthrough Device Designation for six indications and is in pivotal clinical trial for treating adult acute kidney injury, a large patient population in need of effective therapies.
  • Impact: Healthcare sector focusing on critical care, medical devices, and biotechnology markets relevant to organ failure treatments.

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. MTWebcast: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:
[email protected]


Risks

  • Clinical trial outcomes for the NEUTRALIZE-AKI pivotal trial could impact regulatory approval and commercial viability of SCD therapy.
  • Regulatory risks remain as the SCD therapy advances toward approval for adult indications despite Breakthrough Device status.
  • Market adoption of treatments for rare and critical conditions can face reimbursement and commercialization challenges impacting financial results and stock performance.

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