Program strategies and efficiencies – Pharmetheus

A circular PK/PD/PK model explains the exposure of bulevirtide and bile salts in adult patients with Hepatitis D

Absorption, Bioavailability, and Immunogenicity after Subcutaneous Administration: Evaluation of a Subcutaneous Platform within the Open Systems Pharmacology framework

Predicting Reductions in Chronic Obstructive Pulmonary Disease (COPD) Exacerbations from FEV1 – A Model-Based Meta-Analysis of Literature Data from Controlled Randomized Clinical Trials

Towards Industrialisation of Probability of Pharmacological Success (PoPS)

Translating Pharmacometrics to a Pharmacoeconomic Model of COPD

How to Successfully Generate an Alternative Approach to a Thorough QT Study: GLPG1972 as an Example

Physiological Based Pharmacokinetic and Biopharmaceutics Modelling of Subcutaneously Administered Compounds – An Overview of In Silico Models

Overview of Authorized Drug Products for Subcutaneous Administration: Pharmaceutical, Therapeutic, and Physicochemical Properties

Dissolution and Translational Modeling Strategies Toward Establishing an In Vitro-In Vivo Link-a Workshop Summary Report

Assessment of Expected Drug Exposure Relative Maximum Safety Limits in Early Phase Studies

Applications of Clinically Relevant Dissolution Testing: Workshop Summary Report

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