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Biotech / Medical : Pharmos (PARS)
PARS 2.700+13.6%Jan 21 4:00 PM EST

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From: Gabe Fernandez12/3/2004 1:06:30 PM
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Despite the fact that the drug treated groups contained a larger number of more severely injured patients, an analysis of the adverse medical events during the first 10 days post-treatment revealed trends of a lower incidence (p less than 0.2) of mortality (3 vs. 6 patients, or 5.8% vs. 12.2%), fever (88% vs. 98%) and hypotension (19% vs. 33%) in the dexanabinol treated group compared to placebo. (Three more patients in the dexanabinol treated group and one more in the placebo group died later of peripheral complications from other injuries sustained at the time of the brain injury, bringing the total to 6 deaths in the test group, or 11.5%, and 7 deaths in the placebo group, or 14.3%.) ICP management was significantly improved in the dexanabinol group without concomitant reductions in systolic blood pressure. Thus, the mean percentage time with ICP above 25mmHg, a highly negative prognostic factor, was reduced by 60-80% on Days 1-4 post-injury in the dexanabinol treated group compared to placebo. The difference was highly significant (p less than 0.01) on Day 2.

I find this to be a key point in my belief that Dexanabinol will be succesful. The results obtained in Phase II should be able to be better due to the changes in the protocol and the change of GOSE gabe
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