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LN-145-S1 is an investigational, autologous tumor-infiltrating lymphocyte (TIL) therapy developed by Iovance Biotherapeutics. It is a second-generation version of LN-145, manufactured using a modified process that selects for a specific subset of T cells expressing PD-1, which are believed to be enriched for tumor-reactive clones. The therapy is produced as a cryopreserved infusion product at centralized GMP facilities. The treatment protocol involves a non-myeloablative (NMA) lymphodepletion preparative regimen, followed by the infusion of the TIL product and subsequent administration of interleukin-2 (IL-2) to support T-cell expansion and activity. LN-145-S1 is currently being evaluated in Phase II clinical trials for various refractory or relapsed solid tumors, including ovarian cancer, triple-negative breast cancer, and various sarcomas.
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