Regarding HGEN, Dr Patterson stated their therapeu
Post# of 148154
So boards are saying the data is blinded to Humanigen, but endpoint was changed. Did the DSMC just "recommend" changing the endpoint, and Humanigen blindly just said OK. It does result in an endpoint being easier to meet. Someone here said patients on ventilation were excluded in the prior endpoint, but now they added that any patient who advanced to go onto ventilation, would be excluded. That sounds like cheating to me??
Can someone give a review of exclusions we have in our s/c trial? Are patients on ventilation allowed into our trial, seems they would be the hardest to save, and would thus diminish our results?