Ashkan describes differentiation in the trial as using IL-4 and GM-CSF. Can the maturation agent be replaced like that simply because it’s in a patent?
Still finding this hard to believe.
Would that not be like saying when L is approved it will be for clean room production (as in the trial) and for Flaskworks.
ATLnsider, does adding the activation agent poly-ICLC to DCVax-L have any downside as far adverse events since we know that DCVax has very little or no side effects as a cancer treatment which puts NWBIO as a leader in that aspect.