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Axi-Cel.24

Safety and Efficacy of Axicabtagene Ciloleucel in Relapsed/Refractory Large B Cell Lymphoma - Axi-Cel.24

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1013240081
Enrollment
Unknown
Registered
2025-03-28
Start date
2024-12-05
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

relapsed/refractory large B-cell lymphoma. relapsed/refractory large B-cell lymphoma.

Interventions

None listed

Sponsors

Teshima Takanori
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)18 years of age or older at the time of enrollment (2)Patients who meet the indications specified in Guidelines for the Promotion of Optimal Use, axicabtagene ciloleucel (Ref. 1). (3)Patents who are scheduled to receive axi-cel at the participating medical institutions in this study (prospective observational study) (4)Patients who have already received axi-cel administration at a medical institution participating in this study* (retrospective observational study) (5)Patients who have given their free and voluntary consent to participate in this study or patients who do not refuse to participate in the study.

Exclusion criteria

Exclusion criteria: Patients deemed inappropriate as study subjects by the principal investigator in participating medical institution (hereafter referred to as the "site principal investigator"

Design outcomes

Primary

MeasureTime frame
Response rate at 6 months after axi-cel administration (overall response, complete response, partial response)

Contacts

Public ContactHideki Goto

Hokkaido University Hospital

hidekigt0220@gmail.com+81-11-706-7214

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026