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Microcap & Penny Stocks : Pharmos(PARS) -- Ignore unavailable to you. Want to Upgrade?


To: Ariella who wrote (1248)9/17/1998 5:23:00 PM
From: Richard Huth  Respond to of 1491
 
Dear Ariella

Thank you for your comprehensive report. I think you are right by saying PARS offers a good risk/reward ratio, but we should not expect too much within the next months - todays drop seems to reflect the reduced optimism about an assumed strong reaction on possible positive news about HU211.

Actually the market in general (at least for biotech comp.) does look more on positive phase III data and earnings, so unblinding of HU211 might be without any positive effect on stock prices in the short run. Therefore I also agree with you that most important for PARS is finding new partners to reverse the downside trend or PARS.

-- the niche audience that PARS needs to attract is investors who are knowledgeable about pharmaceuticals and biotechs, not folks searching for that 10-bagger in any industry simply because the stock is currently priced under $5. How about if we start a new thread under the pharmaceutical/ biotech section in SI? --

I only can support your proposal - but why not move the complete thread?

-Richard



To: Ariella who wrote (1248)9/17/1998 10:23:00 PM
From: NeuroInvestment  Respond to of 1491
 
Ariella: Your report was thorough and very appreciated. Apparently PARS management does play poker well, because they have indeed unblinded the data and have at least some of the findings analyzed in preliminary fashion.While Dr. Aviv is correct that there has been too much focus on the mortality endpoint (since with the small n, and small number of deaths, it would be hard to reach statistical significance)--PARS has only itself to blame, since they chose to publicize the 12.5% overall mortality rate, and its possible implications. Besides, the FDA loves mortality, because it is easy to measure. Since the Glasgow Coma Scale is such a time-honored medical categorical measure,those scores are critical--though this Phase II needs to impress corporate partners more than the FDA. The FDA is not fond of the kinds of functional measures involved in disability ratings--even though from a clinical/societal cost point of view, these could be the most important. I suspect that these more complicated datasets have not all been worked through yet. Thank you again. NeuroInvestment (www.neuroinv.com)



To: Ariella who wrote (1248)9/18/1998 8:00:00 AM
From: David Israel-Rosen  Respond to of 1491
 
How good is your pocker Face

When Mgt talks about phase III going forward as given. One must conclude that Phase II warranted a move to Phase III

Regards