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FG-3019, a Human Monoclonal Antibody Recognizing Connective Tissue Growth Factor, is Subject to Target-Mediated Drug Disposition.

Authors :
Brenner, Mitchell
Krzyzanski, Wojciech
Chou, James
Signore, Pierre
Fung, Cyra
Guzman, David
Li, Dongxia
Zhang, Weihua
Olsen, David
Nguyen, Viet-Tam
Koo, Carolyn
Sternlicht, Mark
Lipson, Kenneth
Source :
Pharmaceutical Research. Aug2016, Vol. 33 Issue 8, p1833-1849. 17p. 1 Color Photograph, 2 Diagrams, 1 Chart, 6 Graphs.
Publication Year :
2016

Abstract

Purpose: To evaluate and model the pharmacokinetic and pharmacodynamic behavior in rats of FG-3019, a human monoclonal antibody targeting connective tissue growth factor (CTGF). Methods: FG-3019, human CTGF (rhCTGF), or the N-terminal domain of rhCTGF were administered intravenously to rats and concentrations of these proteins as well as endogenous CTGF were determined by immunoassays. FG-3019, or I-labeled FG-3019, and human CTGF (rhCTGF) were co-administered to assess the impact of CTGF on the elimination rate and tissue localization of FG-3019, which was further characterized by immunohistochemical analysis. A PK/PD model for target-mediated elimination of FG-3019 was developed to fit the kinetic data. Results: FG-3019 exhibited non-linear pharmacokinetics in rats. Circulating concentrations of the N-terminal half of CTGF increased after dosing with FG-3019, reached maximal levels after 1-5 days, and returned toward baseline levels as FG-3019 cleared from the circulation, whereas the concentration of intact CTGF was unaffected by administration of FG-3019. Co-administration of rhCTGF dramatically enhanced the rate of FG-3019 elimination, redistributing the majority of I-labeled FG-3019 from the blood to the liver, kidney, spleen and adrenal gland. FG-3019 co-administered with CTGF was found along the sinusoids of the liver and adrenal glands, the capillaries of the kidney glomeruli and in the spleen. A pharmacokinetic model for target-mediated elimination of FG-3019 was used to fit the time courses of FG-3019 and endogenous CTGF plasma concentrations, as well as time courses of rhCTGF and rhCTGF N-fragment after intravenous administration of these species. Conclusions: FG-3019 is subject to target mediated elimination in rats. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07248741
Volume :
33
Issue :
8
Database :
Academic Search Index
Journal :
Pharmaceutical Research
Publication Type :
Academic Journal
Accession number :
116774460
Full Text :
https://doi.org/10.1007/s11095-016-1918-0