BREDA, The Netherlands and GHENT, Belgium, April 24, 2013 /PRNewswire/ --
First program based on proprietary ABDEG™ technology to promote degradation and clearance of disease-causing autoantibodies
arGEN-X, a clinical stage biopharmaceutical company specialized in the discovery and development of highly differentiated human monoclonal antibody therapeutics, announces that it has progressed its second product candidate this year into formal preclinical development.
Complementing its existing pipeline of four human mAb-based programs, arGEN-X has developed ARGX-113 as a human antibody Fc fragment. Exploiting its novel, proprietary technology called ABDEG™, ARGX-113 has been designed to clear and degrade circulating disease-causing autoantibodies. As arGEN-X' first ever ABDEG development program, ARGX-113 is an exciting and novel approach to treating potentially any IgG-mediated autoimmune disease. Such indications could include major autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus, as well as a wide range of serious, orphan diseases for which there are currently insufficient treatment options, such as myasthenia gravis and immune thrombocytopenic purpura.
Development of ARGX-113 was based on preclinical studies originally conducted in the research group of Professor Sally Ward at the University of Texas Southwestern Medical Center, from which arGEN-X licensed the ABDEG technology in 2012. Data generated in Professor Ward's laboratory showed the ability of ABDEGs to markedly reduce inflammation in both preventative and established models of rheumatoid arthritis. Further preclinical studies of ARGX-113 are now being undertaken by arGEN-X, with an IND filing anticipated in 2015.
Tim Van Hauwermeiren, CEO of arGEN-X, said: "The therapeutic potential of ARGX-113 in multiple autoimmune diseases
Copyright©2012 PR Newswire.
All rights reserved