New White Paper: Exploring Translational Capabilities of PDX Models across In Vivo, In Vitro, and Ex Vivo Applications

Expanding PDX Uses for Early Stage and Immuno-Oncology Drug Discovery

New White Paper: Exploring Translational Capabilities of PDX Models across In Vivo, In Vitro, and Ex Vivo Applications

Patient-derived xenografts are recognized as the most predictive preclinical model available for oncology research, providing the animal model system which is closest to human disease. While highly useful for in vivo studies, PDX early stage drug discovery uses have been limited. Immuno-oncology applications are also restricted due to PDX being commonly used in immunodeficient mice.

PDX-derived resources – such as in vitro cell lines and ex vivo platforms- allow PDX key advantages to be exploited across the full preclinical research continuum. PDX-derived cell lines recapitulate clinically relevant features for enhanced predictivity in early stage preclinical research. 3D ex vivo PDX platforms allow cost effective, high throughput drug screening linked to parental model genetics for responder subgroup analysis.

Humanized PDX models are also expanding model use into the immuno-oncology research space, providing multiple research functions allowing the study of the heterogeneity of human disease within a humanized immune system.

Download This White Paper to Understand:

  • How PDX-derived cell lines are developed, and how they are validated against parental models for robust in vitro assays
  • How 3D ex vivo PDX platforms allow rapid screening of large panels of agents, including those targeting the tumor microenvironment through addition of stromal cells
  • How this wide variety of PDX platforms can be used for immunotherapeutic drug development

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