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Optimizing Oncology Therapeutics Through Quantitative Translational and Clinical Pharmacology: Challenges and Opportunities
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences.
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2015 (English)In: Clinical Pharmacology and Therapeutics, ISSN 0009-9236, E-ISSN 1532-6519, Vol. 97, no 1, 37-54 p.Article in journal (Refereed) Published
Abstract [en]

Despite advances in biomedical research that have deepened our understanding of cancer hallmarks, resulting in the discovery and development of targeted therapies, the success rates of oncology drug development remain low. Opportunities remain for objective dose selection informed by exposure-response understanding to optimize the benefit-risk balance of novel therapies for cancer patients. This review article discusses the principles and applications of modeling and simulation approaches across the lifecycle of development of oncology therapeutics. Illustrative examples are used to convey the value gained from integration of quantitative clinical pharmacology strategies from the preclinical-translational phase through confirmatory clinical evaluation of efficacy and safety.

Place, publisher, year, edition, pages
2015. Vol. 97, no 1, 37-54 p.
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Other Basic Medicine
URN: urn:nbn:se:uu:diva-244490DOI: 10.1002/cpt.7ISI: 000347889900012OAI: oai:DiVA.org:uu-244490DiVA: diva2:789887
Available from: 2015-02-20 Created: 2015-02-17 Last updated: 2015-02-20Bibliographically approved

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Friberg, Lena E.
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