Research Topics
| Kathryn L ChapmanSummaryCountry: UK Publications
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Detail Information
Publications
The design of chronic toxicology studies of monoclonal antibodies: implications for the reduction in use of non-human primatesKathryn L Chapman
National Centre for Replacement, Refinement and Reduction of Animals in Research, Gibbs Building, 215 Euston Rd, London NW1 2BE, UK
Regul Toxicol Pharmacol 62:347-54. 2012..They include guidance on the main group size, the inclusion of recovery groups and the number of dose groups used in short and long term chronic toxicology studies...
Preclinical safety testing of monoclonal antibodies: the significance of species relevanceKathryn Chapman
National Centre for the Replacement, Refinement and Reduction of Animals in Research, 20 Park Crescent, London W1B 1AL, UK
Nat Rev Drug Discov 6:120-6. 2007....
Preclinical development of monoclonal antibodies: considerations for the use of non-human primatesKathryn Chapman
National Centre for Replacement, Refinement and Reduction of Animals in Research, London, UK
MAbs 1:505-16. 2009..The addendum of ICHS6 provides a timely opportunity for the scientific and regulatory community to embrace strategies which minimize primate use and increase efficiency of mAb development...
The future of non-human primate use in mAb developmentKathryn L Chapman
National Centre for the Replacement, Refinement and Reduction of Animals in Research, 20 Park Crescent, London W1B1AL, UK
Drug Discov Today 15:235-42. 2010..In this article, the authors review current and future NHP use in mAb development based on surveys, experience and expert opinion and propose a framework that will minimize future NHP use and continue to support science and innovation...
The value of acute toxicity studies to support the clinical management of overdose and poisoning: a cross-discipline consensusKathryn Chapman
National Centre for the Replacement, Refinement and Reduction of Animals in Research, London, UK
Regul Toxicol Pharmacol 58:354-9. 2010....
Working in partnership to advance the 3Rs in toxicity testingAnthony M Holmes
National Centre for the Replacement, Refinement and Reduction of Animals in Research, 20 Park Crescent, London W1B1AL, UK
Toxicology 267:14-9. 2010..This review highlights the mechanisms by which the NC3Rs is working with the pharmaceutical and chemical industries and regulatory authorities to achieve these goals...
A European pharmaceutical company initiative challenging the regulatory requirement for acute toxicity studies in pharmaceutical drug developmentSally Robinson
AstraZeneca, Alderley Park, UK
Regul Toxicol Pharmacol 50:345-52. 2008..The conclusions have been discussed and agreed with representatives of regulatory bodies from the US, Japan and Europe...
