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- Boosting NAFLD Study Enrollment: Leveraging Simulation Tools to Overcome Study Recruitment Hurdles
- Comparing Formulations: How DILIsym® Was Used to Support Current Treatment Guidelines for Overdoses of an Extended-Release Formulation of Acetaminophen
- Confirming Model Optimization: OBESITYsym Predicts the Efficacy and Tolerability of Top Three Weight Loss Drugs
- Dissolution and Dosing: How a Client Used PBPK Modeling to Justify Wider Dissolution Specifications Without Additional Clinical Trials
- How a Sponsor Predicted Bioequivalence of Cladribine Tablets Using GastroPlus® PBPK Modeling
- Improving Type II Diabetes Care: How One Medical Education Provider Identified and Addressed Gaps Using Adaptive Learning
- Predicting Effective Drug Formulations Before Phase 1 Clinical Trials: How Roche Used GastroPlus® to Investigate the Impact of Solubility & Permeability on Bioavailability
- Evaluating Absorption and Exposure Under Altered Gastric pH Conditions: How One Client Used GastroPlus PBPK Modeling to Avoid a DDI Clinical Study
- Evaluating Hepatoxicity Before Late-Stage Trials: How Biohaven Used QST to Ensure Liver Safety and Gain Regulatory Approval
- Identifying the Right Drug Dosage to Prevent DILI: How Astellas Used QST to Progress Fezolinetant to Phase 3 and Beyond
- Strengthening Protocol Compliance: How Simulation-Driven Training Increased Investigator Engagement and Understanding
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