Matthew Wiens, M.A.

Principal Scientist I

Matthew joined Metrum in 2019 as a Research Scientist. He holds an M.A. in Statistics from Boston University. Prior to Metrum, he worked for a variety of startup technology companies where he applied Bayesian methodologies in predictive models based on remote sensing data. His ongoing interests include communicating and leveraging uncertainty from a Bayesian perspective in scalable modeling and simulation projects.

Recent publications by this scientist

Comparison of Virtual Population Generation Methods for Quantitative Systems Pharmacology Models

October 6, 2026

Andrew Tredennick¹, Matthew Weins¹, Timothy Knab¹, Cole Zmurchok¹, Ahmed Elmokadem²
¹ Metrum Research Group, Boston, MA, USA; ² GlaxoSmithKline (GSK), Collegeville, PA, USA

Presented at the 2026 American Conference on Pharmacometrics (ACoP 2026), an International Conference on Pharmacometrics in the US (ICoP – US), on October 14th, 2026.

Virtual populations (VPops) are widely used in quantitative systems pharmacology (QSP) to represent variability in clinical populations and support model calibration and simulation of treatment outcomes. Practical guidance on selecting among algorithms to generate VPops, and understanding their relative performance, remains limited. The objective of this work was to compare commonly used and emerging VPop generation approaches based on data-simulation matching and computation time.

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Pharmacometric Machine Learning: Integrating Neural Networks for Flexible, Advanced Covariate Analysis

June 13, 2025

Presented at ASCPT 2025 Annual Meeting. Neural networks can be integrated with traditional pharmacometric models using several free open-source programming languages. Both Julia and R environments are suitable platforms, but there are tradeoffs regarding development speed, built-in capabilities, and documentation. DCM simplifies the covariate modeling process and uncovers complex, non-linear relationships in computationally efficient workflows.

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A Model-based Framework to Address Dose Modifications

May 19, 2025

This work tackles a central challenge in oncology drug development: predicting  benefit-risk for dosing regimens that have not yet been studied. Semi-mechanistic modeling can be used for this purpose, but model validation is complicated by the presence of safety-driven dose modifications—such as delays and reductions—commonly observed in real-world settings.

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