There wasn't enough patients in GVHD001 alone for 54 above and below the median data points to be put together. I recall that only about 25 of the 54 that were in the GVHD phase 3 trial had blood samples taken. I recall that some of the patients in the phase 3 trial had received product from multiple lots - using data from multiple lots would confound the analysis of patient survival measured against the product lot.
BTW. I mean you no disrespect, but my offer was specifically to LED. (to walk through the science) I have to protect my time. LED might teach me something (even as I try to show her) or not.
But most people that are frequent long term posters on this forum I already have a stereotype about and I don't feel equally inclined to make an effort for all of them.
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