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Treatment of rheumatoid arthritis with PEGylated recombinant human soluble tumour necrosis factor receptor type I: a clinical update
Preclinical studies to date demonstrate that PEGâ[euro][per thousand]sTNF-RI is efficacious in rodent 2-4 and primate 5 models of acute and chronic inflammatory diseases, includingE coli induced septic shock. 6 PEGâ[euro][per thousand]sTNF-RI has demonstrated efficacy in predictive animal models o...
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Published in: | Annals of the rheumatic diseases 2000-11, Vol.59 (suppl 1), p.i41-i43 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Preclinical studies to date demonstrate that PEGâ[euro][per thousand]sTNF-RI is efficacious in rodent 2-4 and primate 5 models of acute and chronic inflammatory diseases, includingE coli induced septic shock. 6 PEGâ[euro][per thousand]sTNF-RI has demonstrated efficacy in predictive animal models of RA at doses as low as 0.3 mg/kg every other day. 2 The results of these and other 7-9 preclinical studies indicate that PEGâ[euro][per thousand]sTNF-RI is a promising treatment for chronic inflammatory diseases. The pharmacokinetics of PEGâ[euro][per thousand]sTNF-RI after single SC administration were dose independent in the range of 100 to 1000â[euro][per thousand]μg/kg after single dose administration, and peak plasma concentrations were observed 48 to 96 hours after the dose. 11 The pharmacokinetics were characterised by a slow absorption rate (absorption half life of 25 hours), a limited volume of distribution (130 ml/kg), a low clearance rate (1.1 ml/h/kg), and a long elimination half life (83 hours). |
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ISSN: | 0003-4967 1468-2060 |
DOI: | 10.1136/ard.59.suppl_1.i41 |