A first-in-human trial for a new solid tumor T cell therapy now has US FDA IND approval, and this webinar presents the data that got it there. The therapy, FastTIL, draws its starting material from malignant pleural effusions, a source usually discarded as clinical waste. Across six consecutive patient samples, an automated cell isolation workflow generated 0.7–3.2 billion viable T cells in just 8–12 days, at 98.3% average purity and 97.6% average viability. These pleural infiltrating T cells stayed functional, showed no signs of exhaustion, and attacked patients' own tumors, the evidence behind the IND clearance.
Attend this webinar to learn how to: