Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
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
Follicular Lymphoma
Lisocabtagene maraleucel
Study Type : | OBSERVATIONAL |
Estimated Enrollment : | 300 participants |
Official Title : | Non-interventional Cohort Study of Patients Treated With Liso-cel (Lisocabtagene Maraleucel) for Relapsed/Refractory Follicular Lymphoma in the Postmarketing Setting |
Actual Study Start Date : | 2025-02-04 |
Estimated Primary Completion Date : | 2044-08-31 |
Estimated Study Completion Date : | 2044-08-31 |
Information not available for Arms and Intervention/treatment
Ages Eligible for Study: | 18 Years |
Sexes Eligible for Study: | ALL |
Accepts Healthy Volunteers: |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
RECRUITING
CIBMTR
Milwaukee, Wisconsin, United States, 53226