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Clinical Trial Summary

The primary objective of this study is to estimate the efficacy of axicabtagene ciloleucel in combination with rituximab, as measured by assessment of response rates in adult participants with relapsed/refractory large B-cell lymphoma.


Clinical Trial Description

Following at least 24 months of assessments after axicabtagene ciloleucel infusion, participants will be asked to rollover to a separate long-term follow-up study (Study KT-US-982-5968). Participants will complete the remainder of the 15-year follow-up assessments in the KT-US-982-5968 study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04002401
Study type Interventional
Source Gilead Sciences
Contact
Status Completed
Phase Phase 2
Start date November 5, 2019
Completion date January 30, 2023

See also
  Status Clinical Trial Phase
Recruiting NCT04836507 - Study of Efficacy and Safety of CRC01 in Adult Large B-cell Lymphoma Patients Phase 1/Phase 2