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Modeling and simulation of abatacept exposure and interleukin-6 response in support of recommended doses for rheumatoid arthritis.

Modeling and simulation of abatacept exposure and interleukin-6 response in support of recommended doses for rheumatoid arthritis. Research Abstract Details 

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  • Modeling and simulation of abatacept exposure and interleukin-6 response in support of recommended doses for rheumatoid arthritis. Abstract Text:

    amit royAmit Roy,diane r mouldDiane R Mould,xiao-feng wangXiao-Feng Wang,lee tayLee Tay,ralph raymondRalph Raymond,marc pfisterMarc Pfister,amit royAmit Roy,diane r mouldDiane R Mould,xiao-feng wangXiao-Feng Wang,lee tayLee Tay,ralph raymondRalph Raymond,marc pfisterMarc Pfister,

    Abatacept is a recombinant soluble fusion protein that inhibits the CD80/CD86:CD28 costimulatory signal required for T cell activation and has demonstrated efficacy in the treatment of rheumatoid arthritis. The objectives of this analysis were to provide support for a body weight-tiered dosing regimen approximating 10 mg/kg by (1) quantifying the effect of body weight on exposure and (2) characterizing the relationship between exposure and serum interleukin (IL)-6 concentration. The abatacept exposure and exposure-response models were developed with 2148 abatacept serum concentrations (from 388 subjects) and 1894 IL-6 serum concentrations (from 799 subjects), respectively, followed by simulation with these models to address the above objectives. Abatacept exposure was characterized by a linear 2-compartmental model, in which clearance was linearly related to body weight. The IL-6 response was characterized by an indirect-response model, in which the IL-6 production rate increased with baseline C-reactive protein levels. Model-based simulations demonstrated that body weight-tiered dosing was desirable to ensure consistent steady-state abatacept trough concentrations across a range of body weights; doses approximating 10 mg/kg (500, 750, 1000 mg for subjects weighing <60, 60-100, and >100 kg, respectively) provided consistent exposure across the body weight groups. In addition, doses >10 mg/kg did not result in further increases in IL-6 suppression. These modeling and simulation results indicate that the body weight-tiered abatacept therapeutic doses approximating 10 mg/kg will ensure consistent abatacept exposure and optimal IL-6 suppression.

    Modeling and simulation of abatacept exposure and interleukin-6 response in support of recommended doses for rheumatoid arthritis. Publishing Authors By Initials

    a royA Roy,dr mouldDR Mould,xf wangXF Wang,l tayL Tay,r raymondR Raymond,m pfisterM Pfister,a royA Roy,dr mouldDR Mould,xf wangXF Wang,l tayL Tay,r raymondR Raymond,m pfisterM Pfister,

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    Modeling and simulation of abatacept exposure and interleukin-6 response in support of recommended doses for rheumatoid arthritis. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of clinical pharmacology

    VOLUME: 47

    Page Numbers: 1408-20

    Journal Abbreviation:

    ISSN: 0091-2700

    DAY: 26

    MONTH: Nov

    YEAR: 2007

    Modeling and simulation of abatacept exposure and interleukin-6 response in support of recommended doses for rheumatoid arthritis. Information

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    LANGUAGE: eng

    NlmUniqueID: 366372

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    Grant and Affiliation Information for Modeling and simulation of abatacept exposure and interleukin-6 response in support of recommended doses for rheumatoid arthritis.

    AFFILIATION: Clinical Discovery, Research and Development, Bristol-Myers Squibb, Princeton, NJ 08543-4000, USA. amit.roy@bms.com

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Clin Pharmacol

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