Abstract |
Tanezumab, a humanized monoclonal anti- NGF antibody, has demonstrated efficacy and safety profiles in Phase III clinical trials of chronic pain. In a 24-week study in non-human primates, morphological observations of sympathetic ganglia showed decreased ganglia volume, decreased neuronal size, and increased glial cell density compared with controls after 3 tanezumab treatments. Using stereological techniques to quantify glial cells, the present 26-week study found no significant difference after weekly treatments in total cervicothoracic ganglia satellite glial cell number between placebo- or tanezumab-treated cynomolgus monkeys. These findings suggest that tanezumab treatment does not result in a true gliosis in sympathetic ganglia.
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Authors | Mark Evans, Mark Butt, Patrice Belanger, Thomas Cummings, Jessica-Lyn Gremminger, Mark Zorbas |
Journal | Autonomic neuroscience : basic & clinical
(Auton Neurosci)
Vol. 218
Pg. 51-53
(05 2019)
ISSN: 1872-7484 [Electronic] Netherlands |
PMID | 30890348
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2019. Published by Elsevier B.V. |
Chemical References |
- Analgesics
- Antibodies, Monoclonal, Humanized
- tanezumab
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Topics |
- Analgesics
(toxicity)
- Animals
- Antibodies, Monoclonal, Humanized
(toxicity)
- Female
- Gliosis
(chemically induced)
- Macaca fascicularis
- Male
- Satellite Cells, Perineuronal
(drug effects, pathology)
- Stellate Ganglion
(drug effects, pathology)
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