Search Results - "Rose, Rachel H."

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  1. 1

    Potential Sources of Inter-Subject Variability in Monoclonal Antibody Pharmacokinetics by Gill, Katherine L., Machavaram, Krishna K., Rose, Rachel H., Chetty, Manoranjenni

    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
  2. 2

    Application of physiologically based pharmacokinetic models for therapeutic proteins and other novel modalities by Rose, Rachel H., Sepp, Armin, Stader, Felix, Gill, Katherine L., Liu, Cong, Gardner, Iain

    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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    Journal Article
  3. 3

    A novel fluorescent histamine H1 receptor antagonist demonstrates the advantage of using fluorescence correlation spectroscopy to study the binding of lipophilic ligands by Rose, Rachel H, Briddon, Stephen J, Hill, Stephen J

    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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    Journal Article
  4. 4

    Quantitative systems pharmacology‐based exploration of relevant anti‐amyloid therapy challenges in clinical practice by Geerts, Hugo, Bergeler, Silke, Walker, Mike, Rose, Rachel H., Graaf, Piet H.

    “…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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    Journal Article
  5. 5

    Learn–confirm in model‐informed drug development: Assessing an immunogenicity quantitative systems pharmacology platform by Franssen, Linnea C., Swat, Maciej J., Kierzek, Andrzej M., Rose, Rachel H., Graaf, Piet H., Grimm, Hans Peter

    “…Immunogenicity against therapeutic proteins frequently causes attrition owing to its potential impact on pharmacokinetics, pharmacodynamics, efficacy, and…”
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    Journal Article
  6. 6

    Pharmacokinetics, Pharmacodynamics and Physiologically-Based Pharmacokinetic Modelling of Monoclonal Antibodies by Dostalek, Miroslav, Gardner, Iain, Gurbaxani, Brian M., Rose, Rachel H., Chetty, Manoranjenni

    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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    Journal Article
  7. 7

    Physiologically-based pharmacokinetic modeling to predict drug-drug interaction of enzalutamide with combined P-gp and CYP3A substrates by Otsuka, Yukio, Poondru, Srinivasu, Bonate, Peter L., Rose, Rachel H., Jamei, Masoud, Ushigome, Fumihiko, Minematsu, Tsuyoshi

    “…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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    Journal Article
  8. 8

    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 by Rose, Rachel H., Turner, David B., Neuhoff, Sibylle, Jamei, Masoud

    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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    Journal Article
  9. 9

    The use of PBPK/PD to establish clinically relevant dissolution specifications for zolpidem immediate release tablets by Paraiso, Rafael L.M., Rose, Rachel H., Fotaki, Nikoletta, McAllister, Mark, Dressman, Jennifer B.

    “…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. 10

    A novel fluorescent histamine H 1 receptor antagonist demonstrates the advantage of using fluorescence correlation spectroscopy to study the binding of lipophilic ligands by Rose, Rachel H, Briddon, Stephen J, Hill, Stephen J

    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
  11. 11

    Bimolecular fluorescence complementation: lighting up seven transmembrane domain receptor signalling networks by Rose, Rachel H, Briddon, Stephen J, Holliday, Nicholas D

    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
  12. 12
  13. 13

    Abstract 2952: Predicting concentration of PARP inhibitors in human tumor tissue using PBPK modeling by Rose, Rachel H., Sun, Kaiming, Li, Linzhong, Gada, Keyur, Wang, Jing Yu, Qiu, Yongchang

    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. 14

    A novel fluorescent histamine H, receptor antagonist demonstrates the advantage of using fluorescence correlation spectroscopy to study the binding of lipophilic ligands by ROSE, Rachel H, BRIDDON, Stephen J, HILL, Stephen J

    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…”
    Get full text
    Journal Article
  15. 15