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Biotech / Medical : XOMA. Bull or Bear? -- Ignore unavailable to you. Want to Upgrade?


To: Cacaito who wrote (14571)9/15/2000 3:49:57 PM
From: manfredhasler  Read Replies (1) | Respond to of 17367
 
Cacaito, Re: ... the low mortality was a very well known feature and very well considered in the study design...as per xoma they were recruting about 80% of the subjects in this group... oviously a logistical nightmare and a financial imposibility for xoma...

Thanks for this information. If it is true we have a management problem in our company. And in that I agree with you.

Just sold my position.

Regards,
Manfred



To: Cacaito who wrote (14571)9/15/2000 6:53:54 PM
From: aknahow  Read Replies (2) | Respond to of 17367
 
Cacaito, why post vague data. Do you consider Glasgow 8 - 11 as low? The two treatment arms were 8-11 and 12 - 15. I was unaware that the mortality rate was only 5% for Glasgow 8 - 11. As a doctor and an honorable person is that your final answer?

By the way XOMA will have hard copies in a few weeks, or you might want to request a pdf copy.

On average it did take six hours for enrollment!

You keep talking about low mortality and disregarding all the subjects that died before getting enrolled.

This eliminated the weakest and made mortality lower in both groups and as the article explained reduced the bacteria load to 1/8 of what it was at its peak and much of the damage from the endotoxin had already been done. So Neuprex was of limited value at that point but still showed compelling benefit.



To: Cacaito who wrote (14571)9/16/2000 11:09:37 AM
From: Robert K.  Read Replies (3) | Respond to of 17367
 
Cacaito>>>>please read this carefully.
Whether it is xomas fault, the fda's fault DOES MOT MATTER.
This drug needs to be available whether STATISTICAL OR NOT.
BPI shows benefit.