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Current practices for QSP model assessment: an IQ consortium survey
Jason R Chan1, Richard Allen2, Britton Boras3
1Global PKPD and Pharmacometrics, Eli Lilly and Company, Indianapolis, IN, 46285, USA. jrchan@lilly.com.
Quantitative Systems Pharmacology (QSP) modeling is vital in drug development. A survey revealed current QSP practices and identified needs for standardization and broader application in late-stage development.
Area of Science:
- Pharmacology
- Computational Biology
- Drug Development
Background:
- Quantitative Systems Pharmacology (QSP) modeling is increasingly utilized in the pharmaceutical industry.
- Standardization of QSP model construction, assessment, and communication is crucial but challenging due to model variability and diverse expertise.
- The IQ Consortium surveyed industry practices to understand current QSP modeling approaches.
Purpose of the Study:
- To present the results of a survey on current Quantitative Systems Pharmacology (QSP) modeling practices within the pharmaceutical and biotechnology industries.
- To provide insights into the methods and applications of QSP models across different drug development stages.
- To identify key areas for future development in QSP modeling.
Main Methods:
- A survey was conducted across the pharmaceutical/biotech industry.
- Data collected focused on current practices, model types, and intended uses of QSP models.
- Results were analyzed to provide insights into practitioner methods.
Main Results:
- The survey revealed diverse current practices in QSP modeling across the industry.
- Insights were gained into methods used by QSP practitioners based on model type and application stage.
- Key areas for future development were highlighted, including integration with statistical methods and standardization.
Conclusions:
- Current QSP modeling practices vary significantly, necessitating further standardization.
- Future developments should focus on integrating statistical methods, standardizing virtual populations, and increasing QSP use in late-stage clinical development and regulatory submissions.
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