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. Author manuscript; available in PMC: 2016 Aug 1.
Published in final edited form as: J Biomol Screen. 2016 Mar 8;21(6):521–534. doi: 10.1177/1087057116635818

Table 1.

Quantitative systems pharmacology platform overview..

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