Tuesday, April 7, 2009

Step in Right Direction

LELYSTAD, The Netherlands, April 6 /PRNewswire/ -- Today, Pepscan reports that it has achieved a major scientific breakthrough through the use of its CLIPS-based synthetic peptide immunogen technology. By constructing synthetic 3D mimics of the ligand binding-site on CXCR7 it has induced functional antibodies against the formerly intractable GPCR target CXCR7. CXCR7 is novel therapeutic target thought to be involved in tumor angiogenesis.

"We are proud and confident with achieving this major breakthrough!" says Professor Rob H. Meloen, Pepscan's founder and Chief Scientific officer. "Since a number of years we have been working on developing our CLIPS technology through which we can synthesize 3D conformational mimics of protein active sites , allowing us to do site-specific immunization to come up with functional antibodies against very difficult targets such as G-protein coupled receptors, as we have now proven with CXCR7." Meloen states that the CLIPS-technology is not limited to application in the GPCR field but also offers possibilities with other therapeutically interesting target such as for instance ion-channels.

Pepscan's Chief Commercial Officer Dr. Peter van Dijken thinks that this technology might unlock a whole new area of interesting therapeutic targets that could so far not be addressed: "One-third of the interesting GPCR targets have proven to be "undrugable" until now. Our CLIPS technology provides a systematic and efficient way to unlock these targets and make them available to antibody therapy, that is a multi-billion dollar playing field to which Pepscan now holds the unique technological key!"

Pepscan indicated today that over the coming period, it will continue to technically and commercially develop its clips-based technology for additional targets and indications.

Therapeutic antibody therapy is well established. Monoclonal antibodies are produced outsid

SOURCE Pepscan Therapeutics B.V.
Copyright©2009 PR Newswire.
All rights reserved

No comments: