A Long-Term Study for Participants Previously Treated With Ciltacabtagene Autoleucel.
To collect long-term follow-up data on delayed adverse events after administration of cilta-cel, and to characterize and understand the long-term safety profile of cilta-cel.
- Rutgers University
Inclusion Criteria: - Participants who have received at least one dose of cilta-cel in a Company-sponsored clinical study - Participants who have provided informed consent for this study
Please note that we have obtained the inclusion and exclusion criteria information from the National Institutes of Health’s clinical trials web site ClinicalTrials.gov. The listed criteria may not necessarily reflect recent amendments to the protocol and the current criteria.
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