RE:RE:RE:Good discussion boysLet's be clear here, they now have 40% CR+IR optimized patient data on 33 patients. @ 450days. They can submit BTD as soon as they have the data FDA requested. Which they may have at this time.38% CR+IR Dara @450 days on the non optimized group of ~40 patients. Pretty good %s and significantly better than keytruda. Ruvdar has few side effects and is a monmo treatment.