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Thirteen-week Intravenous Toxicity Study of a Novel Humanized Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus Monkeys
CS-1008, a humanized monoclonal antibody that is agonistic to human death receptor 5, was intravenously administered to cynomolgus monkeys twice a week for 13 weeks at 3 different dose levels (5, 15 and 42 mg/kg) in order to evaluate its potential toxicity. A control group received phosphate buffere...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Toxicologic Pathology
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234651/ https://www.ncbi.nlm.nih.gov/pubmed/22272006 http://dx.doi.org/10.1293/tox.23.11 |
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author | Kimotsuki, Tomofumi Tanaka, Kohji Sugiura, Tomomi Koyama, Kumiko Nakamura, Takahiro Kamimura, Yasuhiro Takasaki, Wataru Manabe, Sunao |
author_facet | Kimotsuki, Tomofumi Tanaka, Kohji Sugiura, Tomomi Koyama, Kumiko Nakamura, Takahiro Kamimura, Yasuhiro Takasaki, Wataru Manabe, Sunao |
author_sort | Kimotsuki, Tomofumi |
collection | PubMed |
description | CS-1008, a humanized monoclonal antibody that is agonistic to human death receptor 5, was intravenously administered to cynomolgus monkeys twice a week for 13 weeks at 3 different dose levels (5, 15 and 42 mg/kg) in order to evaluate its potential toxicity. A control group received phosphate buffered saline containing 0.01% polysorbate 80. Each of the 4 groups consisted of 3 male and 3 female cynomolgus monkeys. No animal in any group died during the dosing period. No toxic changes in clinical signs, food consumption, body weight, electrocardiography, ophthalmology, urinalysis, hematology, blood chemistry, gross pathology, organ weights or histopathology were noted in any group during the dosing period. In the toxicokinetic analysis, the values for the maximum concentration of CS-1008 in plasma and the area under the curve generally increased with increasing dose. No clear differences in the toxicokinetic parameters or profiles were observed between the sexes. Development of anti-CS-1008 antibodies was not detected in any sample. The no-observed adverse-effect level (NOAEL) of CS-1008 in cynomolgus monkeys under the conditions of this study was concluded to be 42 mg/kg in both sexes, when administered intravenously twice a week for 13 weeks. This study supports the development of CS-1008 as a therapeutic biopharmaceutical. |
format | Online Article Text |
id | pubmed-3234651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Japanese Society of Toxicologic Pathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-32346512012-01-23 Thirteen-week Intravenous Toxicity Study of a Novel Humanized Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus Monkeys Kimotsuki, Tomofumi Tanaka, Kohji Sugiura, Tomomi Koyama, Kumiko Nakamura, Takahiro Kamimura, Yasuhiro Takasaki, Wataru Manabe, Sunao J Toxicol Pathol Original CS-1008, a humanized monoclonal antibody that is agonistic to human death receptor 5, was intravenously administered to cynomolgus monkeys twice a week for 13 weeks at 3 different dose levels (5, 15 and 42 mg/kg) in order to evaluate its potential toxicity. A control group received phosphate buffered saline containing 0.01% polysorbate 80. Each of the 4 groups consisted of 3 male and 3 female cynomolgus monkeys. No animal in any group died during the dosing period. No toxic changes in clinical signs, food consumption, body weight, electrocardiography, ophthalmology, urinalysis, hematology, blood chemistry, gross pathology, organ weights or histopathology were noted in any group during the dosing period. In the toxicokinetic analysis, the values for the maximum concentration of CS-1008 in plasma and the area under the curve generally increased with increasing dose. No clear differences in the toxicokinetic parameters or profiles were observed between the sexes. Development of anti-CS-1008 antibodies was not detected in any sample. The no-observed adverse-effect level (NOAEL) of CS-1008 in cynomolgus monkeys under the conditions of this study was concluded to be 42 mg/kg in both sexes, when administered intravenously twice a week for 13 weeks. This study supports the development of CS-1008 as a therapeutic biopharmaceutical. The Japanese Society of Toxicologic Pathology 2010-03 2010-04-05 /pmc/articles/PMC3234651/ /pubmed/22272006 http://dx.doi.org/10.1293/tox.23.11 Text en 2010 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Original Kimotsuki, Tomofumi Tanaka, Kohji Sugiura, Tomomi Koyama, Kumiko Nakamura, Takahiro Kamimura, Yasuhiro Takasaki, Wataru Manabe, Sunao Thirteen-week Intravenous Toxicity Study of a Novel Humanized Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus Monkeys |
title | Thirteen-week Intravenous Toxicity Study of a Novel Humanized
Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus
Monkeys |
title_full | Thirteen-week Intravenous Toxicity Study of a Novel Humanized
Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus
Monkeys |
title_fullStr | Thirteen-week Intravenous Toxicity Study of a Novel Humanized
Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus
Monkeys |
title_full_unstemmed | Thirteen-week Intravenous Toxicity Study of a Novel Humanized
Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus
Monkeys |
title_short | Thirteen-week Intravenous Toxicity Study of a Novel Humanized
Anti-Human Death Receptor 5 Monoclonal Antibody, CS-1008, in Cynomolgus
Monkeys |
title_sort | thirteen-week intravenous toxicity study of a novel humanized
anti-human death receptor 5 monoclonal antibody, cs-1008, in cynomolgus
monkeys |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234651/ https://www.ncbi.nlm.nih.gov/pubmed/22272006 http://dx.doi.org/10.1293/tox.23.11 |
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