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S-033
The Dose and Dosing Schedule Selection for an Investigational Immuno-Oncology Drug Based on a Pharmacokinetics and Pharmacodynamic Model of Tolerance

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S-040
Time-to-event analysis of iron homeostasis to inform survival in cancer patients

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M-056
Time-to-event exposure-response based clinical utility index framework to facilitate optimal dose selection

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M-023
Towards uncertainty assessment-based acceptability thresholds for model validation?

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M-005
Transforming Pharmacometric Processes to deliver medicines to patients: Balancing Speed, Quality, and Innovation

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M-058
Transforming the Development of Targeted Protein Degraders: The Translational Power of PK/PD Modeling beyond the Human Dose Projection

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M-034
Translating PROTACs: Relating in vitro Potency to Protein Degradation Kinetics

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M-009
Translation of a Preclinical Tumor Growth Inhibition Model to a Clinical Setting: Two Approaches to Incorporate Resistance in a Tumor Dynamics Model

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T-006
Translational two-pore PBPK model to characterize whole-body disposition of different-size oligonucleotide therapeutics

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