RecruitingNCT06788652

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

Non-interventional Cohort Study of Patients Treated With Lisocabtagene Maraleucel (Liso-cel) for Relapsed/Refractory Mantle Cell Lymphoma in the Post-Marketing 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 understand the long-term safety and effectiveness of lisocabtagene maraleucel (liso-cel) for the treatment of Mantle Cell Lymphoma (MCL).


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • • 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 Criteria2

  • 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

BIOLOGICALLisocabtagene maraleucel

According to US Prescribing Information


Locations(1)

Center for International Blood and Marrow Transplant Research (CIBMTR)

Milwaukee, Wisconsin, United States

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NCT06788652


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