PPHM reconstituted data...60% increase in MOS and STAT SIG...What do you suppose would have happened without the dose switch(pronounced sabotage)? NY Academy Science presentation reiterated >110% increas in MOS? Is that what the FDA sees? Was it 80 patients until the "act" was committed? Not saying approval but how about a breakthrough designation? Maybe? A year lost? I guess the FDA approves all corrupted phase II trial results and awards fast track status with 2 interim lookins? WHY DIDN'T the FDA force a redo? Did they see something or are they into risking patients lives? I don't know...do you? tia wook