Stopped: Terminated due to slow accrual.
This phase Ib trial studies whether anti-CD19-chimeric antigen receptor (CAR) lentiviral vector-transduced autologous T cells (JCAR014) and durvalumab are safe in combination and can work together in treating patients with non-Hodgkin lymphoma that has returned after a period of improvement (relapsed) or has not responded to previous treatment (refractory). JCAR014 is made of each patient's immune cells (T cells) that have a new gene added to them in a laboratory, which programs them to kill lymphoma cells. Durvalumab is a type of drug called a monoclonal antibody, targeted to PD-L1 that may help immune cells attack cancer cells more effectively and thus help JCAR014 work better.
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Count of Participants Who Experienced Adverse Events
Timeframe: 28 days post last infusion of Durvalumab, up to 1 year
Dose Limiting Toxicity (DLT) Rates
Timeframe: 28 days post first infusion of Durvalumab (for participants in Group 1) or 28 days post infusion of JCAR (for participants in Group 2)
Highest Treatment Dose Administered on Study
Timeframe: 28 days
Maximum JCAR014 Cmax by Flow Cytometry
Timeframe: Up to 12 months
Area Under the Curve (AUC) of JCAR014 by Flow Cytometry
Timeframe: Up to 28 days
Maximum JCAR014 Cmax in Blood by Quantitative Polymerase Chain Reaction (qPCR) Analysis
Timeframe: Up to 12 months
AUC of JCAR014 Cells by qPCR Analysis
Timeframe: Up to 28 days
Time to Loss of JCAR014 Detection in Blood by qPCR Analysis
Timeframe: Up to 12 months, +/- 30 days