Spots Global Cancer Trial Database for Study Evaluating SC262 in Subjects With r/r Non-Hodgkin's Lymphoma (VIVID)

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Trial Identification

Brief Title: Study Evaluating SC262 in Subjects With r/r Non-Hodgkin's Lymphoma (VIVID)

Official Title: A Phase 1 Study Evaluating SC262, a Hypoimmune, Allogeneic CD22-directed CAR T Cell Therapy, in Relapsed and/or Refractory Non-Hodgkin's Lymphoma (VIVID)

Study ID: NCT06285422

Conditions

Non Hodgkin's Lymphoma

Large B-cell Lymphoma

Interventions

SC262

Study Description

Brief Summary: SC262-101 is a Phase 1 study to evaluate SC262 safety and tolerability, anti-tumor activity, cellular kinetics, immunogenicity, and exploratory biomarkers.

Detailed Description: This is an open-label, single arm, Phase 1, first-in-human (FIH) study to evaluate the safety and tolerability of SC262 administered intravenously (IV) following a standard lymphodepleting chemotherapy regimen of cyclophosphamide and fludarabine in subjects with Non Hodgkin's Lymphoma (NHL) who have received no more than 1 prior CD19-directed Chimeric Antigen Receptor T-Cells (CAR T) cell therapy. This study will be conducted in 2 parts. Dose finding using a 3+3 design in subjects with NHL. Dose expansion to further evaluate safety and efficacy at the recommended phase 2 dose (RP2D) in subjects with Large B-Cell Lymphoma (LBCL).