With modeling and simulation, your existing data can answer many important drug development questions and potentially save your program significant time and money.
Existing and prospectively collected data from your compound, as well as literature data on similar compounds, can be leveraged to provide important insights on product safety and effectiveness due to variability in drug concentrations. These insights can also be used to select dose regimens to optimize benefit-risk ratio, assess the need to adjust the dose for intrinsic and extrinsic factors, inform clinical trial design, predict trial outcomes, and more.
Use this toolkit to learn how modeling and simulation can make clinical trials more efficient and even be used to potentially avoid certain clinical trials completely.
Download Nuventra’s Modeling & Simulation Toolkit: