Evaluate Safety of Axicabtagene Ciloleucel Reinfusion (Axi-Cel-2) in Patients With Relapsed and/or Refractory Second Line High-Risk Non-Hodgkin Lymphoma After Standard of Care Axi-Cel

PHASE1RecruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

May 23, 2023

Primary Completion Date

April 1, 2038

Study Completion Date

April 1, 2038

Conditions
Non-Hodgkin LymphomaLarge B-cell Lymphoma
Interventions
DRUG

Axicabtagene Ciloleucel

Subjects will receive a re-infusion of Axi-Cel (Axi-Cel-2) if signs and symptoms of cytokine release syndrome (CRS) and Immune Effector Cell Associated Neurotoxicity Syndrome (ICANS) are ≤ grade 1.

Trial Locations (1)

94305

RECRUITING

Stanford University, Palo Alto

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Kite Pharma

UNKNOWN

lead

Stanford University

OTHER