May 10, 2005, Piscataway, NJ -- Provid Pharmaceuticals Announces Celiac Disease Program and Grant.
Provid Pharmaceuticals Inc. has been awarded an SBIR grant from the National
Institute of Digestive Disorders and Kidney Disease (NIDDK) to pursue a novel
therapeutic strategy for celiac disease (celiac sprue). Celiac is a
disease of gluten intolerance that affects approximately 1/500 individuals,
causing severe gastrointestinal and other reactions to gluten ingestion.
Currently, celiac disease can only be treated by strict dietary abstinence
from wheat and other grain products. The disease is also characterized
by a genetic association to the MHC class II molecule, HLA-DQ2. Binding
of gluten-derived peptides to HLA-DQ2 is the first step in triggering an
immune response to gluten peptides. The immune response from autoreactive
T cells that results from this trigger leads to destruction of the lining
of the small intestine and to a variety of other symptoms. The Provid
project seeks to block this first step with an orally adminstered inhibitor
of HLA-DQ2.
Provid’s plan to develop a drug for celiac disease is based on the company’s
strategy for developing therapeutic drugs for other autoimmune diseases.
The approach is based on blocking antigen binding to disease-associated MHC
molecules by Provid’s small molecule peptide mimetics. The company
has other programs for multiple sclerosis (partnered with a pharmaceutical
company) and rheumatoid arthritis in addition to the new celiac program.
Provid is a chemistry-based drug discovery company with expertise in all
aspects of medicinal chemistry, structure-based drug design, lead optimization,
protein biochemistry and assay development. Provid pursues internal programs
for the discovery of novel therapeutics for autoimmune diseases based on
a platform technology in the field of peptide mimetics. The company
also offers collaborative discovery services to biotech companies and academic
groups that need medicinal chemistry expertise to transform their biologically
driven research into drug molecules.
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