In particular, R788 had an ACR20 response rate of 66% (p<0.001) at the 100mg bid dose (primary dose being carried forward) at 6 months compared to Arzerra's ACR20 score of 50%. Note that this data comes from RIGL's TASKi2 study, which was a success, not the "incongruent" TASKi3 study comprised of biologic failures. Arzerra may have a better safety profile although it's not oral, like R788.