Nonclinical Development of Novel Biologics, Biosimilars and Specialty Biologics

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9780123948106: Nonclinical Development of Novel Biologics, Biosimilars and Specialty Biologics

Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics is a complete reference devoted to the nonclinical safety assessment of novel biopharmaceuticals, biosimilars, vaccines, cell and gene therapies and blood products. This book compares and contrasts these types of biologics with one another and with small molecule drugs, while incorporating the most current and essential international regulatory documents. Each section discusses a different type of biologic, as well as early characterization strategies, principles of study design, preclinical pharmacokinetics and pharmacodynamics and preclinical assays. An edited book that is authored by leading experts in the field, this comprehensive reference provides critical insights to all researchers involved in early through late stage biologics. It provides in-depth coverage of the process of nonclinical safety assessment and comprehensive reviews of each type of biopharmaceutical. It contains the most pertinent international regulatory guidance documents for nonclinical evaluation. It covers early de-risking strategies and designs of safety assessment programs for novel biopharmaceuticals and vaccines, as well as follow-on biologics or "biosimilars". It offers a multi-authored book with chapters written by qualified experts in their respective fields.

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".brings nonclinical testing of biological and follow-on biological drugs, vaccines plus cell and gene therapy drugs right up to date. It is written in a very readable, yet highly scientific manner and most of the relevant publications.on the topic are referenced.Overall, a 'must read' book for all in the nonclinical field of developing biological drugs."--btsNews, June 2014 "Researchers in pharmaceuticals, toxicology, and other biological sciences summarize the current status of developing medicines from biological material, pointing out where the process is different from developing small-molecule medicines and where it is the same. The topics include regulatory guidelines and their application in the non-clinical evaluation of biological medicines, early de-risking strategy for novel biotherapeutics."--Reference & Research Book News, December 2013

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Plitnick, Lisa (Editor)/ Herzyk, Danuta (Editor)
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Plitnick, Lisa
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Book Description Elsevier Science Publishing Co Inc, United States, 2013. Hardback. Book Condition: New. 239 x 196 mm. Language: English . Brand New Book. Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics is a complete reference devoted to the nonclinical safety assessment of novel biopharmaceuticals, biosimilars, vaccines, cell and gene therapies and blood products. This book compares and contrasts these types of biologics with one another and with small molecule drugs, while incorporating the most current and essential international regulatory documents. Each section discusses a different type of biologic, as well as early characterization strategies, principles of study design, preclinical pharmacokinetics and pharmacodynamics and preclinical assays. An edited book that is authored by leading experts in the field, this comprehensive reference provides critical insights to all researchers involved in early through late stage biologics. Bookseller Inventory # LIB9780123948106

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Plitnick, Lisa
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Book Description Elsevier Science Publishing Co Inc, United States, 2013. Hardback. Book Condition: New. 239 x 196 mm. Language: English . Brand New Book. Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics is a complete reference devoted to the nonclinical safety assessment of novel biopharmaceuticals, biosimilars, vaccines, cell and gene therapies and blood products. This book compares and contrasts these types of biologics with one another and with small molecule drugs, while incorporating the most current and essential international regulatory documents. Each section discusses a different type of biologic, as well as early characterization strategies, principles of study design, preclinical pharmacokinetics and pharmacodynamics and preclinical assays. An edited book that is authored by leading experts in the field, this comprehensive reference provides critical insights to all researchers involved in early through late stage biologics. Bookseller Inventory # LIB9780123948106

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Plitnick, Lisa M., Ph.D. (EDT)/ Herzyk, Danuta J., Ph.D. (EDT)/ Arora, Vikram, Ph.D. (CON)/ Brandon, Eugene P., Ph.D. (CON)
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Book Description Elsevier Science Publishing Co Inc 2013-08-29, San Diego, 2013. hardback. Book Condition: New. Bookseller Inventory # 9780123948106

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PLITNICK, LISA; HERZYK, DANUTA
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Book Description Academic Press, 2013. Hardback. Book Condition: NEW. 9780123948106 This listing is a new book, a title currently in-print which we order directly and immediately from the publisher. Bookseller Inventory # HTANDREE0893544

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PLITNICK, LISA; HERZYK, DANUTA
Published by Academic Press (2013)
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Book Description Academic Press, 2013. Hardback. Book Condition: NEW. 9780123948106 This listing is a new book, a title currently in-print which we order directly and immediately from the publisher. Bookseller Inventory # HTANDREE01197463

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Lisa Plitnick
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Book Description Oxford Elsevier LTD Sep 2013, 2013. Buch. Book Condition: Neu. 244x192x30 mm. Neuware - Nonclinical Development of Novel Biologics, Biosimilars and Specialty Biologics is a timely and comprehensive look at the process of nonclinical safety assessment of different types of biopharmaceuticals or biologics. Biologic drugs are a growing and crucial part of the overall pharmaceutical market, largely and generally because they are slightly cheaper to produce, provide higher profit margins and have a higher approval rate than conventional drugs. This reference includes the latest international guidance documents on nonclinical evaluation and a comprehensive review of vaccines, novel biopharmaceuticals, biosimilars and other biologics. By incorporating early de-risking strategies and principles of study design for each type of biopharmaceutical and comparing each to small molecule drugs, this multi-authored book is a valuable resource for all those involved in biologics development. 416 pp. Englisch. Bookseller Inventory # 9780123948106

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