Potential FDA Approval of Atara's Tab-cel Therapy: A Game-Changer for Future Growth and CAR T Program RevitalizationWe remain optimistic about the likelihood of FDA approval for tab-cel, as EBV+ PTLD is an ultra-rare indication and we believe Atara has been able to address manufacturing concerns raised by the FDA. Importantly, Atara has been able to show comparability with additional clinical data, but a request for even more clinical data (or a new Phase 3 trial) from the FDA remains a risk, although moderate in our view.