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Thursday, October 6, 2022

Lyell Immunopharma Announces FDA Clearance of its IND for Cancer Treatment

 

  • Autologous TIL therapy enhanced with Lyell’s Epi-R™ reprogramming technology designed to create polyclonal T cell populations with properties of durable stemness and improved function

  • Phase 1 trial to initially enroll patients with relapsed and/or refractory metastatic or locally advanced melanoma and subsequently expand into non-small cell lung cancer and colorectal cancer

  • Initial data presentation expected in 2024


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