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An expert panel hosted by
Customizing first-line BTK inhibitors for CLL
with Gilles Salles, Paolo Ghia, and Francesc Bosch
Wednesday, October 23, 2024
18:30-19:30 BST
This independent educational activity is supported by Pharmacyclics LLC, an AbbVie Company and Janssen Biotech. All content is developed independently by the faculty. The funder is allowed no influence on the content of this activity.
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On May 28, 2022, it was announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval for the use of tisagenlecleucel, a chimeric antigen receptor (CAR) T-cell product, for the treatment of adult patients with relapsed or refractory follicular lymphoma who have previously received ≥2 lines of systemic therapy.1 To conform with the accelerated approval program, continued approval in this setting may be dependent upon verification and proven clinical benefit in a confirmatory trial(s). This approval marks the third indication that tisagenlecleucel has received FDA approval for, and it remains the only CAR T-cell therapy approved in both adult and pediatric settings. The approval is based on pivotal data obtained from the phase II ELARA trial (NCT03568461),1 previously reported on the Lymphoma Hub.
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