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resected or fulgurated, as feasible within 90 days prior to treatment allocation.\n* Acceptable baseline organ function.\n\nCohort B Key Inclusion Criteria:\n\n* Pathologically confirmed BCG-exposed high-risk high-grade NMIBC (i.e., CIS with or without Ta\u002FT1 disease or high-grade Ta\u002FT1 papillary-only disease without CIS) within 90 days of treatment allocation.\n* All visible disease must be resected, and all CIS resected or fulgurated, as feasible within 90 days prior to treatment allocation.\n* Acceptable baseline organ function.\n\nCohort CX Inclusion Criteria\n\n* Pathologically confirmed high-risk high-grade BCG-unresponsive or BCG-exposed NMIBC (i.e., CIS with or without Ta\u002FT1 disease or high-grade Ta\u002FT1 papillary-only disease without CIS) within 90 days of treatment allocation.\n* All visible disease must be resected, and all CIS resected or fulgurated, as feasible within 90 days prior to treatment allocation.\n* Acceptable baseline organ function.\n\nKey Exclusion Criteria (Both Cohorts):\n\n* Current or past history of muscle-invasive, locally advanced or metastatic bladder cancer.\n* High-grade urothelial carcinoma in the upper urinary tract or prostatic urethra within 24 months or T2 in upper tract within 48 months or any history of locally advanced\u002F nodal or metastatic disease in the upper urinary tract.\n* Significant immunodeficiency.\n* Pregnant or breastfeeding.\n* Cohort CX Only: serial intravesical gemcitabine within 24 months","ALL","18 Years",{"count":1016,"type":1017},325,"ESTIMATED","INTERVENTIONAL",[1020],"PHASE2","This is a Phase 2, Multi-Arm, Multi-Cohort, Open-Label Study to Evaluate the Safety and Efficacy of Cretostimogene Grenadenorepvec in Participants with High-Risk Non-Muscle-Invasive Bladder Cancer.",[1023],"High-Risk Non-Muscle-Invasive Bladder Cancer",[1025],"Bladder 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