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Replies to #3685 on Biotech Values
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ciciagt

09/21/04 11:47 PM

#3691 RE: rkcrules2001 #3685

Another company interested in preventing the damage to intellect following CABG is ATSI. (As an aside, if you do any DD on ATSI you will likely find an investment based purely on it's open pivot heart valve will be a long term positive for your portfolio. imo)

http://www.atsmedical.com/
MINNEAPOLIS, April 27 /PRNewswire-FirstCall/ -- ATS Medical, Inc. (Nasdaq: ATSI), a leader in mechanical heart valve technology and related cardiac surgical accessories, announced today that it has agreed to terms with Swedish research firm ErySave AB for exclusive development, licensing and marketing of a new patented health care technology for cardiac surgery procedures........
The platform, PARSUS, Particle Separation by Ultrasound, enables highly qualitative filtering, by ultrasound waves, of potentially dangerous particles suspended in blood. This technique could potentially be used in all patients requiring a cardiac surgery procedure such as heart valve replacement or repair and coronary artery by pass.......
Open heart surgery results in the release of tiny particles of fat (lip micro emboli) into the patient's blood. In the brain, these particles can block fine capillaries, obstructing blood flow to vital areas resulting in oxygen deficit and potential neurological injury and dysfunction. The PARSUS technology effectively filters out these hazardous lipid microemboli by harmlessly separating them from the blood by ultrasound waves before the blood is transfused back into the patient. Elimination of these lipid microemboli particles makes autotransfusion more viable. Current methods of filtering the patient's blood, by centrifuge or filter, do not effectively remove these particles.
http://www.erysave.com/site_flash.html


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DewDiligence

09/22/04 12:48 AM

#3692 RE: rkcrules2001 #3685

The control treatment in PARS’ pump-head trial is indeed a placebo:

http://www.pharmoscorp.com/news/pr/pr040803.html
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Patients are being randomized one-to-one to receive a single dose of either 150 mg. dexanabinol or placebo prior to initiation of CPB. Each patient will be evaluated prior to surgery, at discharge, at six weeks, and at three months following surgery to assess the incidence and degree of post-surgical CI. The degree of cognitive impairment will be assessed using a sophisticated and validated battery of computerized neuropsychological tests including attention deficit, memory loss and speed of reaction.
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