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Spectral Medical Inc T.EDT

Alternate Symbol(s):  EDTXF

Spectral Medical Inc. is a Canada-based late-stage theragnostic company advancing therapeutic options for sepsis and septic shock. The Company develops and commercializes a treatment for septic shock utilizing its Endotoxin Activity Assay (EAA) diagnostic and the Toraymyxin therapeutic (PMX). PMX is a therapeutic hemoperfusion device that removes endotoxin, which can cause sepsis, from the bloodstream and is guided by the Company’s EAA. 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. It has pioneered the development of biochemical markers for the clinical syndrome known as septic shock. It is continuing its legacy business of manufacturing and selling certain proprietary reagents. It develops, produces and markets recombinant proteins, antibodies and calibrators. These materials are sold for use in research and development, as well as in products manufactured by other diagnostic companies.


TSX:EDT - Post by User

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Comment by Stocktreeon Jul 14, 2016 2:05pm
160 Views
Post# 25053097

RE:The EUPHRATES trial

RE:The EUPHRATES trial
Thanks for the link TechOne. I started reading and stumped on a sentence regarding the result of the EUPHAS trial and it’s termination. I wonder if you (or anyone else) could help me understand if it actually is at odds with the second excerpt (and why), taken from an article of the Journal of the American Medical Association on the same trial.
 
From
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066268/
 
Also, the absolute risk of death at 28 days improved significantly from 53% in the conventional therapy group to 32% in the PMX-DHP treated group [19]. This result, albeit encouraging, is considered controversial as the trial was stopped early after an interim analysis showed the mortality difference in a secondary endpoint.
 
 
From
https://jama.jamanetwork.com/article.aspx?articleid=184078#RESULTS
 
The [interim] analysis triggered the stopping rule based on a statistically significant reduction in mortality in the polymyxin B hemoperfusion group. Results were discussed with the president of the ethics committee (Internal Institutional Ethical Commission of the coordinating center), who declared it unethical to deprive a potentially beneficial therapy to a group of patients that carry high mortality. The study was thus terminated.
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