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Titlebook: Development of Antibody-Based Therapeutics; Translational Consid Mohammad A. Tabrizi,Gadi G. Bornstein,Scott L. Kla Book 20121st edition Sp

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书目名称Development of Antibody-Based Therapeutics
副标题Translational Consid
编辑Mohammad A. Tabrizi,Gadi G. Bornstein,Scott L. Kla
视频video
概述Examines important considerations necessary for the design of effective translational strategies during the development of antibody-based therapeutics.Improves the understanding of generation and engi
图书封面Titlebook: Development of Antibody-Based Therapeutics; Translational Consid Mohammad A. Tabrizi,Gadi G. Bornstein,Scott L. Kla Book 20121st edition Sp
描述Translational strategies for development of antibody-based therapeutics should allow understanding of the relationship between the ‘unit dose’ and ‘unit effect’ with respect to both beneficial and deleterious effects from early stages of development. The flow of information from later to earlier stages of development should provide opportunities to facilitate selection of more effective novel and next-generation drug candidates. Selection and evaluation of relevant biomarkers in early preclinical development in "relevant" animal models should allow for identifying potential risks to humans and establishing safe First-In-Human (FIH) dosing strategies. Hence, integration of knowledge with respect to target antigen properties such as antigen distribution, expression profile, kinetic properties, target pharmacology, antigen isoforms and pharmacological redundancy in health and disease, as well as antibody design criteria, such as antibody isotype, affinity, PK/PD and safety is a critical necessity for the design of effective translational strategies. Additionally, these factors will further offer critical differentiating characteristics for next-generation antibodies, and novel technol
出版日期Book 20121st edition
关键词Antibody; Antibody-Based; Bornstein; Considerations; Development; Klakamp; Tabrizi; Therepeutic; Translation
版次1
doihttps://doi.org/10.1007/978-1-4419-5955-3
isbn_softcover978-1-4899-9113-3
isbn_ebook978-1-4419-5955-3
copyrightSpringer Science+Business Media, LLC, part of Springer Nature 2012
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Grundbegriffe des preußischen Wegerechtsth a diverse array of soluble or cell-associated target antigens. Much like traditional small molecule drugs, a major challenge during the development of antibody-based therapeutics is maintaining an effective information flow and translation of accumulated knowledge throughout the various developme
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Die Bermutung der unvordenklichen ZeitStates. With the passing of time, new technological developments together with competition for finite markets have continually raised the bar for the specifications of newly introduced antibodies. Our intent in this review is to provide a historical perspective on the technologies that have generate
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,Vormundschaftliche Armutsbekämpfung,fects of antibody-based drugs. Advances in protein engineering technologies afforded investigators the ability to overcome problems associated with introducing foreign antibodies into humans. These efforts included antibody chimerization, humanization, and the more recent development of human antibo
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,Vormundschaftliche Armutsbekämpfung,–antigen complexes for drug candidate optimization and the design of clinical dosing strategies. For measuring the dissociation equilibrium constants of mAbs binding reversibly to antigens, two premier technologies are commonly used: Biacore surface plasmon resonance (SPR) and the solution-based kin
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https://doi.org/10.1007/978-3-8349-9876-7he earliest stages of the discovery process for antibody-based therapeutics. Selection of the adequate affinity for a functional antibody should allow achievement of the maximum therapeutic benefit at a dose associated with a manageable cost of goods and the intended route of administration. Applica
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Grundfragen der Familientherapieeep understanding of both the biology and the pathology of disease is essential for target identification and validation. This knowledge enables the rationale design of antibody therapeutic attributes including mechanism of action (MOA), specificity, potency, isotype subclass, affinity, and half-lif
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