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Biotech / Medical : VD's Model Portfolio & Discussion Thread -- Ignore unavailable to you. Want to Upgrade?


To: Vector1 who wrote (7748)3/18/2000 7:08:00 PM
From: Ward Knutson  Read Replies (1) | Respond to of 9719
 
V1,

Taxol and all other front-line therapy agents have dose-limiting side effects. This drug has a selective uptake action that differentiates it from today's cytotoxic agents. I firmly believe you will, as you see further results, see that this drug is capable of finding a role even more significant than that of the several hundred million dollars "salvage" therapy indications could bring. Take notice of the Prostate study, in this patient population the drug has shown to be very well tolerated. This implies that those yet to be heavily pre-treated (as would be the case as front-line therapy) with other chemo agents (Prostate patients are handled front-line by hormonal therapies) can be, and have been, treated with significant dosing over numerous courses of therapy of MGI-114 exhibiting both a high degree of efficacy and safety. Too early to be certain, but I encourage you to look deeply into the mounting body of supporting data and research supporting MGI-114.

<<It is critical to understand MGI 114's mechanism of action so that analogs can be derived that are more specific and have fewer dose limiting side effects.>>

Already in progress, in fact there are currently at least nine analogs at the NCI under pre-clinical evaluation - all have shown significant anti-tumor activity. MGI has stated as a goal for 2000 to identify at least one of these to advance in the development process.

This will be an interesting AACR Presentation:
Sunday, April 2, 2000
Presidential Address, "Pancreatic Cancer: New Targets, New Treatments" Daniel D. Von Hoff 8:00 - 9:00 a.m.

Ward