00:27:32 EDT Sat 18 May 2024
Enter Symbol
or Name
USA
CA



Spectral Medical Inc
Symbol EDT
Shares Issued 278,576,261
Close 2023-09-29 C$ 0.34
Market Cap C$ 94,715,929
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Spectral Medical's Nosenzo resigns as director

2023-10-02 12:15 ET - News Release

Mr. Chris Seto reports

SPECTRAL MEDICAL PROVIDES BOARD UPDATE

Spectral Medical Inc.'s John Nosenzo will be stepping down from Spectral Medical's board of directors due to health reasons, effective Oct. 1, 2023.

Mr. Nosenzo has been a valuable member of the board of directors, and the company expresses deep gratitude for his invaluable contributions. However, in light of the circumstances surrounding his health, Mr. Nosenzo has made the difficult decision to step down from his position, effective immediately.

Chris Seto, chief executive officer of Spectral Medical, commented: "While we are sad to see John leave our board of directors, given his tremendous career accomplishments, we are also grateful for his significant contributions to the company. John has served on our board since August, 2020, and his knowledge and expertise have been extremely valuable as we developed our commercialization strategy. We wish him all the best, as he focuses on his family and personal interests."

The company does not intend to replace Mr. Nosenzo's position on the board of directors.

About Spectral Medical Inc.

Spectral is a phase 3 company seeking United States Food and Drug Administration (FDA) approval for its unique product for the treatment of patients with septic shock, Toraymyxin (PMX). PMX is a therapeutic hemoperfusion device that removes endotoxin, which can cause sepsis, from the bloodstream and is guided by the company's endotoxin activity assay (EAA), the only FDA-cleared diagnostic for the risk of developing sepsis.

PMX is approved for therapeutic use in Japan and Europe and has been used safely and effectively on more than 340,000 patients to date. In March, 2009, Spectral obtained the exclusive development and commercial rights in the United States for PMX and, in November, 2010, signed an exclusive distribution agreement for this product in Canada. In July, 2022, the U.S. FDA granted breakthrough device designation for PMX for the treatment of endotoxemic septic shock. Approximately 330,000 patients are diagnosed with septic shock in North America each year.

We seek Safe Harbor.

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