AN OPEN-LABEL MULTICENTER PHASE 2 STUDY EVALUATING THE EFFICACY AND SAFETY OF CRG-022 A CD22-DIRECTED AUTOLOGOUS CHIMERIC ANTIGEN RECEPTOR (CAR) T-CELL THERAPY IN PARTICIPANTS WITH RELAPSED/REFRACTORY LARGE B-CELL LYMPHOMA AFTER CD19-DIRECTED CAR T-CELL THERAPY
Brief description of study
CD19-directed autologous CAR T-cell therapy has changed the treatment landscape for patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL). Nonetheless, up to 60% of patients undergoing autologous CD19-directed CAR T-cell therapy experience disease progression due to treatment resistance, including CD19-negative relapse; outcomes for these patients are poor. Therapy directed at an alternative B-cell-specific antigen may be able to overcome resistance to CD19-directed therapy. CRG-022 is an autologous CAR T-cell product targeting CD22, a common B-cell antigen widely expressed in LBCL. This study aims to evaluate the safety and the efficacy of CRG-022 in the treatment of participants with R/R LBCL that has progressed after CD19-directed CAR T-cell therapy, an area of high unmet need.
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