Iovance Biotherapeutics Inc. announced new real-world clinical data for Amtagvi® (lifileucel), a one-time T cell therapy for advanced melanoma. The data, presented at the 2026 Tandem Meetings of the American Society for Transplantation and Cellular Therapy (ASTCT®) and the Center for International Blood and Marrow Transplant Research (CIBMTR®), demonstrated an objective response rate $(ORR)$ of 44% in a real-world cohort of 41 previously treated advanced melanoma patients. Patients who received Amtagvi earlier in their treatment course showed higher response rates, with a 52% ORR reported after two or fewer prior lines of therapy, compared to 33% after three or more lines. These real-world findings build on the previously reported 31% ORR from the C-144-01 clinical trial, which supported Amtagvi’s accelerated approval by the U.S. FDA in February 2024. Iovance is also conducting the Phase 3 TILVANCE-301 trial to further evaluate Amtagvi in frontline advanced melanoma.
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. Iovance Biotherapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9649984) on February 05, 2026, and is solely responsible for the information contained therein.