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NCT06788652Recruiting

A Study of Patients With Relapsed/Refractory Mantle Cell Lymphoma Treated With Lisocabtagene Maraleucel in the Post-Marketing Setting

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

Start Date

2/4/2025

Completion Date

9/30/2044

Summary

The purpose of this study is to understand the long-term safety and effectiveness of lisocabtagene maraleucel (liso-cel) for the treatment of Mantle Cell Lymphoma (MCL).

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: • Participants must have been treated in the postmarketing setting with at least 1 infusion of lisocabtagene maraleucel (Liso-cel) used for the treatment of Mantle Cell Lymphoma (MCL) according to the FDA-approved indication and dose range (ie, per the US Prescribing Information) and with a product meeting the specifications for commercial release approved in the USA Exclusion Criteria: * Participants known to be participating in investigational studies at the time of liso-cel infusion. * Participants treated with non-conforming CAR T-cell product.

Interventions

BIOLOGICAL

Lisocabtagene maraleucel

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Conditions

Mantle Cell Lymphoma (MCL)

Locations

Center for International Blood and Marrow Transplant Research (CIBMTR)

Milwaukee, Wisconsin 53226

United States