To: Slugger who wrote (9520 ) 4/4/1999 2:03:00 PM From: Cacaito Read Replies (1) | Respond to of 17367
Slugger, The total mortality of 57, I gave example in post 9520 is an approximation of what could be a reasonable outcome based on the phase II bpi trial(4% mortality) and the historical mortality in standard treatment (30% to 60%) depending on stage of shock. Then I used conservative numbers to arrive to a trial sample on each group by Glasgow scores. The 130 patients was a DSMB meeting review for safety issues, not a Xoma goal for efficacy. The 200 patients was a rough estimate (and probably based on slow recruitment)ending trial earlier has been in the speculation of Murphy, and this thread (check post 5214). And this was for extremely good outcomes. Check post 6523, already at the time of that presentation (first half of 1998) it was already considered a number in the 300s range. The stratification of the trial was a good move, but it will take more patients to complete it. Some argue for a total mortality in the low 30s, this speculation is baseless, unless one assume close to zero mortality in the bpi group, and this is highly unlikely, but possible. This trial is ongoing as any trial of its king would. Trying to read into it with the purpose of timing the stock is useless. Either one believes in the known basic and clinical sciences behind bpi, or one does not. I believe in bpi efficacy, but less than 10% of my money is on it (and as a gauge is a poor one, given my assets is a small amount, not what people call smart money). I am just waiting for the trial completion to make a decision to invest more or not. Xoma is a highly speculative investment, is a make it or brake it type of company. Xoma is not going to gamble their existence in a rush trial leaving poor data, they already had the E5 debacle, almost going out of business for it. By the way, does anyone has the data on the E5 trials? I have never seen anything but animal studies in press.