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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

Bullboard Posts
Post by somweyungguyon Oct 05, 2016 2:24pm
132 Views
Post# 25312993

Write Dr. Jeffrey Shuren @ the FDA for clarification

Write Dr. Jeffrey Shuren @ the FDA for clarificationAsk him why a clear promotor of CTSO would be allowed to serve on the Euphrates Trial DSMB

If he doesn't answer send 60 Minutes an e-mail and ask them to investigate.

I've had enought of this ridiculous BS

CTSO is the ticker symbol NOT "BFD"...

It's important "Beech Boy"...it is 5 X times the value of our investment

Furthermore, the gentleman on their website sat on our DSMB committee

It's REAL F'ing important Beech Boy


GREAT NEWS from our American Friends - CTSO!!

Positive top line data..yes VERY positive..It is completely SAFE!

Congrats to them and ALL involved!

No wonder they are worth 5 X TIMES the value of Spectral

CytoSorbents Announces Positive Top-line Safety Data from REFRESH I Cardiac Surgery Trial

2016-10-05 07:00 ET - News Release

First Randomized Controlled Trial to Demonstrate Safety of Intra-operative CytoSorb Use in High Risk Cardiac Surgery

MONMOUTH JUNCTION, N.J., Oct. 5, 2016 /PRNewswire/ -- CytoSorbents Corporation (NASDAQ: CTSO), a therapeutic device company commercializing its CytoSorb® blood purification cartridge to control deadly inflammation in critically-ill and cardiac surgery patients, announced positive top-line safety data from its recently completed randomized, controlled REFRESH I cardiac surgery feasibility and safety trial. Following a detailed review of all reported adverse events in a total of 46 enrolled patients, the independent Data Safety Monitoring Board (DSMB) found no safety concerns related to the CytoSorb device, achieving the primary safety endpoint of the trial and fulfilling a key requisite to move forward with a larger, definitive pivotal study. In addition, the therapy was well-tolerated and technically feasible, implementing easily into the cardiopulmonary bypass circuit without the need for an additional external blood pump. This study represents the first randomized controlled trial demonstrating the safety of intra-operative CytoSorb use in patients undergoing high risk cardiac


Read more at https://www.stockhouse.com/companies/bullboard#sDOFlTfVGZyeRBji.99

Read more at https://www.stockhouse.com/companies/bullboard#quqgeFCddD7MEBRt.99


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