To: Vector1 who wrote (7208 ) 11/21/1999 6:45:00 PM From: Ward Knutson Read Replies (1) | Respond to of 9719
<<I am surprised that that do not have a pharma partner since they do not have the resources to take the drug through phase III themselves.>> That is entirely a FALSE statement. I suggest you call Bill Brown, CFO. <<I guess I expected better initial results in the phase IIs>> 114 is shrinking a broad-range of tumors in human clinical trials. We have already seen evidence of 70% plus Pancreatic, 60% plus Ovarian, 47% non-small cell lung, and a profound impact on PSA levels in very sick prostate cancer patients. We also have been told by the Company that they are extremely encouraged by the number of courses of therapy patients are receiving. Patients in Phase II studies ONLY continue to receive courses of treatment IF they are experiencing disease stabilization OR better, tumor shrinkage. Obviously long-term dosing implies tolerability of the drug, ie. safety. We have observed nothing but trends which point to efficacy and safety, in other words the precursor to approval. This is to say nothing for the other 9 analogs that the Company owns rights and patents on, all of which are showing activity in pre-clinical studies. Why do you think the NCI continues to expand the amount of their resources being used in the development of acylfulvenes? The expansion is well beyond the scope of the initial contractual agreement with MGI. If you are Chuck Blitzer and you have strong indications of a very potent anti-cancer agent, you wait and deliver the solid anticipated clinical data to the prospective partners before you ink a deal. This only increases the appetite of the partner - making the marketing partner a far more lucrative deal. V1, it is clear to me you have very little understanding of what is really going on at MGI Pharma especially as it relates to the development of the acylfulvenes. The facts are stacked in direct contradiction to your impressions.