TIL Therapy Development Solutions
Configurable TIL therapy development spanning tumor processing, TIL isolation/rapid expansion, functional and phenotypic qualification, and release criteria—paired with manufacturing‑aligned process development and IND documentation to de‑risk scale‑up for solid‑tumor programs.
TIL Therapy Development Solutions
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Creative Biolabs offers translational Tumor‑Infiltrating Lymphocyte (TIL) therapy development, delivering a configurable workflow from tumor tissue processing and TIL isolation/expansion to potency testing, phenotype profiling, and release criteria definition.
Manufacturing‑minded methods (e.g., rapid expansion protocols, cytokine/feeder strategies) and analytics (exhaustion markers, clonality, tumor reactivity) help de‑risk scalability while supporting IND documentation and technology transfer.
Key Features / Benefits
- Tissue dissociation → TIL isolation → expansion (REP) → functional qualification
- Phenotype, reactivity and clonality assessment; cytokine secretion and killing assays
- Manufacturing‑aligned process development and comparability packages
- Regulatory documentation support for IND‑enabling studies
Relevant Applications
- Autologous TIL programs for solid tumors requiring robust expansion and potency
- Method transfer, scale‑up, and release testing for clinical manufacturing
- Biomarker and mechanism studies on TIL phenotype and persistence
