The disconnect between preclinical models and clinical outcomes remains a key challenge in drug development, especially as therapies become more complex. Traditional in vitro and in vivo models often lack the physiological relevance needed to predict drug-induced liver injury (DILI), a leading cause of candidate failure. In this webinar, experts explore how human and animal liver microphysiological systems (MPS) enhance DILI risk prediction and support more confident clinical progression.
Topics to be covered
- Current limitations of traditional models in predicting clinical drug safety
- How MPS improve the physiological relevance of preclinical liver models
- Where organ-on-a-chip and MPS technologies fit into the drug development pipeline
- Considerations for implementing liver MPS in early safety testing strategies