Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
B-cell Non Hodgkin Lymphoma
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

OUTLINE: Patients receive anakinra subcutaneously (SC) daily on days 0-13 and axicabtagene ciloleucel via infusion on day 0. After completion of axicabtagene ciloleucel infusion, patients are followed up periodically for up to 90 days.

OUTLINE: Patients receive anakinra subcutaneously (SC) daily on days 0-13 and axicabtagene ciloleucel via infusion on day 0. After completion of axicabtagene ciloleucel infusion, patients are followed up periodically for up to 90 days.

Tracking Information

NCT #
NCT04359784
Collaborators
  • National Cancer Institute (NCI)
  • Swedish Orphan Biovitrum
Investigators
Principal Investigator: Jordan Gauthier Fred Hutch/University of Washington Cancer Consortium