Table 1.
Intrinsic Characteristics | Impact |
---|---|
Modular integration of fundamental principles from pharmacology and systems biology |
Quantitative, network-centric, mechanistic understanding of biology underlying disease progression |
Iterative use of experimental and computational models | Biomarkers and drug-target interactions mechanistically linked to disease-specific mechanisms of progression |
Anticipation of resistance mechanisms, drug-drug interactions, and off-target activity |
|
Integration of data from unbiased, biased, and published studies |
Increased opportunity for repurposing drugs, minimizing toxicity, and pursuing optimal targets |
Integration of data across multiple spatial and temporal scales |
Preclinical models account for heterogeneity, complex cellular context, and multicellular interactions |
Based on patient data | Improved patient stratification and efficiency for demonstrating proof of concept in appropriately defined patient cohorts in phase II and III trials |
Continued progress toward personalized v. population medicine |