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Published on 4/25/2006 in the Prospect News Biotech Daily.

CepTor: Myodur's proof-of-concept data significant in Muscular Dystrophy

By E. Janene Geiss

Philadelphia, April 25 - CepTor Corp. said Tuesday that proof-of-concept data was statistically significant for its targeted calpain-inhibiting drug Myodur when tested in animals with Duchenne Muscular Dystrophy.

In the mouse, an animal model with a genetic defect identical to Duchenne Muscular Dystrophy, the company showed muscle tissue preservation on histopathology and a statistically significant increase in myofiber (muscle fibers) diameter in treated versus non-treated mice, according to a company news release.

Duchenne Muscular Dystrophy is a fatal muscle-wasting disease caused by abnormally high levels of calpain activity.

The company presented this data at a recent medical conference in San Diego, officials said. It also presented data demonstrating the efficiency of its cell-targeted technology through in-vitro studies in human cell lines showing that its calpain inhibitor is 50 times to 100 times more potent when targeted with a carnitine carrier compared to when delivered alone.

The company also presented information involving the development of a biomarker that can specifically measure excess calpain activity, officials said.

"As we continue to push toward the [Investigational New Drug application], we become increasingly excited about the potential we may have here to treat a very important disease," Bill Pursley, chairman and chief executive officer of CepTor, said in the release.

CepTor is a Hunt Valley, Md., development-stage biopharmaceutical company that develops and commercializes proprietary, cell-targeted therapeutic products to treat neuromuscular and neurodegenerative diseases with a focus on orphan diseases.


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