Clinical Trial DataThe gem/nab-paclitaxel cohort was impacted by informative censoring of the control arm which led to an imbalance in the number of patients in the active and control arms, which made this cohort of patients unsuitable for analysis.
Financial ResourcesNT219 is Phase 2 ready though company likely needs additional resources to advance this program.
Safety ConcernsThere was a higher number of Grade 3+ treatment-emergent adverse events rate of 94% compared to 67% for control, which included higher rates of diarrhea and fatigue.