Observational Study of Lisocabtagene Maraleucel for Mantle Cell Lymphoma
This study is looking at the long-term safety and how well lisocabtagene maraleucel (liso-cel) works for people with Mantle Cell Lymphoma (MCL) that has come back or not responded to previous treatments. Lisocabtagene maraleucel is a type of CAR T-cell therapy. You can join this study if you are 18 or older and have already received at least one infusion of lisocabtagene maraleucel for MCL, following the approved guidelines. The main goal is to track any side effects over a long period, up to 15 years. This study is currently observational, meaning researchers are watching what happens to people who have already received the treatment, rather than giving new treatment. The study aims to include about 300 participants, but its current status is unclear.
- Study design
- This is an observational study, meaning researchers are collecting information from people who have already received treatment. It aims to include about 300 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for adverse events (side effects) for up to 15 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Study of Patients With Relapsed/Refractory Mantle Cell Lymphoma Treated With Lisocabtagene Maraleucel in the Post-Marketing Setting
At a glance
Conditions
NCT06788652
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Center for International Blood and Marrow Transplant Research (CIBMTR)
Milwaukee, Wisconsinno site contact published
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Bristol-Myers Squibb · STUDY_DIRECTOR · Bristol-Myers Squibb
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Exclusion
What this trial measures
- Adverse events (AEs)Up to 15 years