merger of
Encode Pharmaceuticals. In March 2008, Raptor acquired an exclusive,
worldwide license to the intellectual property and development rights for
use of Cysteamine and DR Cysteamine for the treatment of NASH. The Company
plans to initiate a Phase 2a clinical trial in collaboration with the
University of California, San Diego ("UCSD") to evaluate Cysteamine in
patients with NASH. In May 2008, Raptor received orphan drug designation
from the FDA for DR Cysteamine for the treatment of Huntington's Disease.
About Raptor Pharmaceuticals Corp.
Raptor Pharmaceuticals Corp. ("Raptor") is a development-stage
biopharmaceutical company leveraging novel drug-targeting platforms and
reformulated therapeutics to improve treatment outcomes among patients with
liver disorders, infectious diseases, cancer, and various orphan
indications. The Company's clinical division advances internally developed
and in-licensed clinical-stage product candidates towards marketing
approval and commercialization and is currently involved in clinical trials
in patients with aldehyde dehydrogenase ("ALDH2") deficiency as part of
Raptor's Convivia(TM) program and nephropathic cystinosis as part of
Raptor's DR Cysteamine program. Raptor's preclinical division bioengineers
novel drug candidates and drug-targeting platforms derived from the human
receptor-associated protein ("RAP") and related proteins to target cancer,
neurodegenerative disorders and infectious diseases. Raptor's preclinical
programs include HepTide(TM), WntTide(TM) and NeuroTrans(TM).
For additional information, please visit http://www.raptorpharma.com.
FORWARD LOOKING STATEMENTS
This document contains forward-looking statements as that term is
defined in the Private Securities Litigation Reform Act of 1995. These
statements relate to future events or our future results of operation or
future financial performance, including, but not limit
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