Gilead Sciences Inc. announced new results from analyses of Yescarta® (axicabtagene ciloleucel) for patients with relapsed/refractory large B-cell lymphoma (R/R LBCL). The findings, which were presented at the 67th American Society of Hematology $(ASH)$ Annual Meeting and Exposition, include data from a combined analysis of the four-year ZUMA-7 Phase 3 study and the two-year ALYCANTE Phase 2 study. The results demonstrate that second-line Yescarta therapy provides consistent safety, efficacy, and quality of life benefits across a broad range of R/R LBCL patients, including those ineligible for high-dose chemotherapy and autologous stem cell transplant.
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. Gilead Sciences Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251207097497) on December 07, 2025, and is solely responsible for the information contained therein.
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