Search Results - "Rose, Rachel H."
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Potential Sources of Inter-Subject Variability in Monoclonal Antibody Pharmacokinetics
Published in Clinical pharmacokinetics (01-07-2016)“…Understanding inter-subject variability in drug pharmacokinetics and pharmacodynamics is important to ensure that all patients attain suitable drug exposure to…”
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Journal Article -
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Application of physiologically based pharmacokinetic models for therapeutic proteins and other novel modalities
Published in Xenobiotica (03-08-2022)“…The past two decades have seen diversification of drug development pipelines and approvals from traditional small molecule therapies to alternative modalities…”
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A novel fluorescent histamine H1 receptor antagonist demonstrates the advantage of using fluorescence correlation spectroscopy to study the binding of lipophilic ligands
Published in British journal of pharmacology (01-03-2012)“…BACKGROUND AND PURPOSE Fluorescent ligands facilitate the study of ligand–receptor interactions at the level of single cells and individual receptors. Here, we…”
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4
Quantitative systems pharmacology‐based exploration of relevant anti‐amyloid therapy challenges in clinical practice
Published in Alzheimer's & dementia : translational research & clinical interventions (01-04-2024)“…INTRODUCTION Addressing practical challenges in clinical practice after the recent approvals of amyloid antibodies in Alzheimer's disease (AD) will benefit…”
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5
Learn–confirm in model‐informed drug development: Assessing an immunogenicity quantitative systems pharmacology platform
Published in CPT: pharmacometrics and systems pharmacology (01-02-2023)“…Immunogenicity against therapeutic proteins frequently causes attrition owing to its potential impact on pharmacokinetics, pharmacodynamics, efficacy, and…”
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Pharmacokinetics, Pharmacodynamics and Physiologically-Based Pharmacokinetic Modelling of Monoclonal Antibodies
Published in Clinical pharmacokinetics (01-02-2013)“…Development of monoclonal antibodies (mAbs) and their functional derivatives represents a growing segment of the development pipeline in the pharmaceutical…”
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Physiologically-based pharmacokinetic modeling to predict drug-drug interaction of enzalutamide with combined P-gp and CYP3A substrates
Published in Journal of pharmacokinetics and pharmacodynamics (01-10-2023)“…Enzalutamide is known to strongly induce cytochrome P450 3A4 (CYP3A4). Furthermore, enzalutamide showed induction and inhibition of P-glycoprotein (P-gp) in in…”
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Incorporation of the Time-Varying Postprandial Increase in Splanchnic Blood Flow into a PBPK Model to Predict the Effect of Food on the Pharmacokinetics of Orally Administered High-Extraction Drugs
Published in The AAPS journal (01-07-2017)“…ABSTRACT Following a meal, a transient increase in splanchnic blood flow occurs that can result in increased exposure to orally administered high-extraction…”
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The use of PBPK/PD to establish clinically relevant dissolution specifications for zolpidem immediate release tablets
Published in European journal of pharmaceutical sciences (01-12-2020)“…Zolpidem is a non-benzodiazepine hypnotic agent which has been shown to be effective in inducing and maintaining sleep in adults and is one of the most…”
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Journal Article -
10
A novel fluorescent histamine H 1 receptor antagonist demonstrates the advantage of using fluorescence correlation spectroscopy to study the binding of lipophilic ligands
Published in British journal of pharmacology (01-03-2012)“…BACKGROUND AND PURPOSE Fluorescent ligands facilitate the study of ligand–receptor interactions at the level of single cells and individual receptors. Here, we…”
Get full text
Journal Article -
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Bimolecular fluorescence complementation: lighting up seven transmembrane domain receptor signalling networks
Published in British journal of pharmacology (01-02-2010)“…There is increasing complexity in the organization of seven transmembrane domain (7TM) receptor signalling pathways, and in the ability of their ligands to…”
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Journal Article Conference Proceeding -
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Applications of linking PBPK and PD models to predict the impact of genotypic variability, formulation differences, differences in target binding capacity and target site drug concentrations on drug responses and variability
Published in Frontiers in pharmacology (26-11-2014)“…This study aimed to demonstrate the added value of integrating prior in vitro data and knowledge-rich physiologically based pharmacokinetic (PBPK) models with…”
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Abstract 2952: Predicting concentration of PARP inhibitors in human tumor tissue using PBPK modeling
Published in Cancer research (Chicago, Ill.) (01-07-2019)“…Abstract Poly (ADP-ribose) polymerase (PARP) inhibitors exert their effect intracellularly within tumor, thus sufficient tumor penetration is essential for a…”
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Journal Article -
14
A novel fluorescent histamine H, receptor antagonist demonstrates the advantage of using fluorescence correlation spectroscopy to study the binding of lipophilic ligands
Published in British journal of pharmacology (01-03-2012)“…Fluorescent ligands facilitate the study of ligand-receptor interactions at the level of single cells and individual receptors. Here, we describe a novel…”
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Journal Article -
15
The Effect of Agonist Activation and Homodimerisation on the Membrane Diffusion of the Human Histamine H1 Receptor
Published in Biophysical journal (01-02-2009)Get full text
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