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Biotech / Medical : GZMO

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To: scaram(o)uche who wrote (101)9/17/1999 4:19:00 PM
From: jeffbas  Read Replies (1) of 438
 
Rick, can you draw any inference that because ATIII is known to be safe for humans that aaATIII will also be safe, and if so will this have positive implications for the length of time needed for the entire discovery to (potential) market timeline?

Is it good to have AS/ES ahead in the sense that if something is heard about the progress there, GZMO can take advantage of it, even to the extent of abandoning the project if this class of compounds is ineffective in humans?

Is it bad to have AS/ES ahead because if this class of compounds is effective GZMO has to demonstrate that it is an improvement over
AS/ES to get FDA approval? I noticed with interest the lower dosage required -- would this be such an "improvement"?
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