RecruitingNCT06794268

A Study to Patients With Relapsed/Refractory Follicular Lymphoma Treated With Liso-cel (Lisocabtagene Maraleucel) in the Post Marketing Setting

Non-interventional Cohort Study of Patients Treated With Liso-cel (Lisocabtagene Maraleucel) for Relapsed/Refractory Follicular Lymphoma in the Postmarketing Setting


Sponsor

Juno Therapeutics, Inc., a Bristol-Myers Squibb Company

Enrollment

300 participants

Start Date

Feb 4, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to characterise the long-term safety of lisocabtagene maraleucel, focusing on patients treated in the approved follicular lymphoma (FL) indication, and will be part of post-marketing liso-cel pharmacovigilance activities


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This observational study follows patients with relapsed or refractory follicular lymphoma — a slow-growing blood cancer — who have received a commercially available CAR-T cell therapy called lisocabtagene maraleucel (liso-cel) outside of a clinical trial. The goal is to collect real-world data on outcomes and safety. **You may be eligible if...** - You have been treated with the CAR-T therapy liso-cel for follicular lymphoma (Grade 1, 2, or 3a) in a real-world, post-approval setting in the United States **You may NOT be eligible if...** - You were treated with liso-cel as part of another clinical trial - You were treated for Grade 3b follicular lymphoma (a more aggressive subtype) - You received a non-standard or non-conforming version of the CAR-T product Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALLisocabtagene maraleucel

As per product label


Locations(1)

CIBMTR

Milwaukee, Wisconsin, United States

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NCT06794268


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