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Spectral Medical Inc
Symbol EDT
Shares Issued 278,644,428
Close 2024-05-03 C$ 0.43
Market Cap C$ 119,817,104
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Spectral enrolls seven patients in Tigris in April

2024-05-06 11:40 ET - News Release

Mr. Chris Seto reports

SPECTRAL MEDICAL PROVIDES APRIL TIGRIS TRIAL UPDATE

Spectral Medical Inc. has provided an update on the company's Tigris trial, a phase 3 follow-on study evaluating the use of polymyxin B hemoperfusion (PMX) in a randomized controlled trial of adults treated for endotoxemia and septic shock.

Enrolment:

  • Robust enrolment activity continuing throughout 2024:
    • 105 patients enrolled at end of April, 2024:
      • Record monthly enrolment with seven patients enrolled in April;
      • 24 patients enrolled in 2024 so far -- represents the most robust enrolment rates since the start of the Tigris study.
  • With 45 patients to full enrolment, the company is entering the final push to fully enroll and finish the Tigris trial:
    • To support sustained enrolment, Spectral hosted an in-person investigator meeting March 12 and 13 in conjunction with the 29th International Conference on Advances in Critical Care Nephrology in San Diego;
    • In-person meeting well attended with multiple stakeholders present, including: principal investigators and clinical research co-ordinators from existing and new trial sites; CRO, Beaufort; and representatives from the company's strategic partner Baxter.

Trial sites:

  • Continued progress opening additional high-quality clinical sites:
    • Recently onboarded the University of Virginia;
    • Two pending sites in the pipeline finalizing contracting and training;
    • Spectral clinical team focused on trial site management activities to ensure that Tigris sites have the support and resources to enroll patients as efficiently as possible.

About Spectral Medical Inc.

Spectral is a phase 3 company seeking U.S. Food and Drug Administration 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.

We seek Safe Harbor.

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