drugset / Trial / NCT03761056

Study to Evaluate the Efficacy and Safety of Axicabtagene Ciloleucel as First-Line Therapy in Participants With High-Risk Large B-Cell Lymphoma

NCT03761056

Phase 2 Completed 42 enrolled Kite, A Gilead Company
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to estimate the efficacy of axicabtagene ciloleucel in participants with high-risk large B-cell lymphoma. After the end of KTE-C19-112 (ZUMA-12), participants who received an infusion of axicabtagene ciloleucel will complete the remainder of the 15-year follow-up assessments in a separate long-term follow-up study, KT-US-982-5968.

Timeline

Start
2019-01-29
Primary completion
2023-10-12
Completion
2023-10-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Axicabtagene Ciloleucel Cell therapy 2e+06 cells/kg Intravenous
Subject Axicabtagene Ciloleucel Cell therapy 2e+08 cells Intravenous
Background Cyclophosphamide Other / unclassified 500 mg/m2 Intravenous
Background Fludarabine Small molecule 30 mg/m2 Intravenous

Indications