Lyell Immunopharma Inc. has announced new clinical and translational data from its ongoing trial of rondecabtagene autoleucel (ronde-cel, LYL314) in patients with large B-cell lymphoma. The results were presented at the 67th American Society of Hematology $(ASH)$ Annual Meeting and Exposition. As of the September 5, 2025, data cutoff, ronde-cel demonstrated a 93% overall response rate and a 76% complete response rate in the third- or later-line setting, with a median progression-free survival of 18 months. In the second-line setting, patients achieved an 83% overall response rate and a 61% complete response rate. The safety profile was reported as manageable, with no high-grade cytokine release syndrome and 5% or fewer patients experiencing Grade 3 or higher ICANS following dexamethasone prophylaxis. Presentation materials and a webcast replay will be available on the Lyell website.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Lyell Immunopharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9598165-en) on December 07, 2025, and is solely responsible for the information contained therein.
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