Advancing Immunotherapy Research: Syngeneic Tumor Models for Preclinical Success
Empower Your Research with TD2’s Syngeneic Tumor Models
TD2 executes data driven in vivo studies using well characterized syngeneic tumor models. These models are critical for evaluating immune checkpoint inhibitor efficacy within a fully functional immune system. Performing preclinical in vivo studies using meticulously characterized syngeneic models ensures relevance and reliability in preclinical oncology research. By utilizing TD2 for preclinical immunotherapy studies, researchers can obtain accurate insights into tumor-immune interactions, facilitating the development of novel immunotherapeutics.
Features and Benefits:
- Fully Characterized: TD2 executes preclinical in vivo studies in syngeneic tumor models that are fully characterized for gene expression, TIL baseline populations, and response to common immune checkpoint inhibitors.
- Diverse Tumor Types: A wide selection of well characterized syngeneic tumor models enables research across a wide range of cancer types, enhancing the applicability of findings. TD2 has experience performing successful in vivo studies using difficult to develop models such as TC-1 and commonly used models like MC38.
- Predictive Value for Clinical Efficacy: Performing preclinical in vivo studies using well characterized syngeneic tumor models enables a researcher to move into the clinic with confidence. Giving them access to insights to potential clinical outcomes of immunotherapeutic agents.
- Enhanced Immunotherapy Evaluation: TD2’s use of syngeneic models facilitates detailed analysis of immunotherapy efficacy, offering a comprehensive view of how these treatments interact with the immune system to target cancer cells. This feature is especially beneficial for developing and testing new immune checkpoint inhibitors, providing a robust platform to optimize therapeutic strategies before clinical trials.