InterMune Presents Preclinical Data Identifying A Principal Mechanism Of Anti-Fibrotic Action For Pirfenidone
March 11th, 2010 by approachgrownInterMune, Inc.
(Nasdaq: ITMN) announced results today from preclinical studies of
pirfenidone that identify a molecular butt of the compound’s
anti-fibrotic interest. Pirfenidone is the Company’s insignificant molecule drug
seeker that is being developed for the treatment of patients with
idiopathic pulmonary fibrosis (IPF) in its Phase III program, DIMENSIONS. The
in vitro studies present that pirfenidone suppresses fibrogenesis
through selective inhibition of the p38-gamma mitogen-activated protein
kinase (MAPK). The results will be included in a presentation made today by
InterMune scientists at GTCbio’s Protein Kinases in Drug Discovery and
Development Conference being held in Boston, Massachusetts.
In IPF, fibrosis occurs when wound healing cells deposit collagen,
which leads to peculiar scarring of the lung tissues. Previous inquiry
demonstrates that pirfenidone reduces blood plasma levels in vivo of
TGF-beta and Interleukin-4, two pro-fibrotic signaling molecules, and
significantly inhibits TGF-beta-induced collagen synthesis in vitro.
Pirfenidone was also shown to control production of TNF-alpha, a molecule
intricate with inflammation. In this late-model work, InterMune scientists have
shown a principal anti-fibrotic mechanism of action of pirfenidone as the
restraint of the p38- gamma kinase. In weather of this, InterMune studies
have demonstrated specificity of pirfenidone for the p38-gamma isoforms in
biochemical kinase assays as well as the attenuation of TGF-beta induced
collagen integrating following treatment of cells with pirfenidone. These new
studies demonstrate a link between inhibition of p38-gamma and a specific
marker of fibrogenesis.
“Extensive industry-wide analysis has demonstrated that the p38-alpha
isoform regulates numerous biological processes that participate an important duty
in inflammatory diseases. The anti-fibrotic mechanism of act of
pirfenidone involving selective barrier of p38-gamma and its associated
inhibition of collagen synthesis may test to be an important basics in
the treatment of fibrotic lung diseases. InterMune’s ongoing ROOM
trials are designed to ascertain if the anti-fibrotic activity of
pirfenidone purpose occur in weighty benefit for patients with IPF,” said
Lawrence M. Blatt, Ph.D., Chief Scientific Officer of InterMune.
Relative to IPF
IPF is a disabling and finally fatal disease that affects
close to 83,000 people in the United States, with approximately 30,000
remodelled cases developing each year. InterMune estimates there is a significant
IPF population in Europe. Those diagnosed with IPF are usually between the
ages of 40 and 70, and the infection tends to affect men more than women. IPF
causes inflammation and scarring (fibrosis) in the lungs, hindering a
person’s talent to convert oxygen and causing shortness of breath
(dyspnea) and cough. IPF is a progressive disease, meaning that over someday,
lung scarring and symptoms increase in severity. The disease is very
deadly, with a median survival time from diagnosis of two to five years,
and a five-year survival under any circumstances of around 20 percent. There are
currently no drugs approved by the U.S. Food and Drug Conduct (FDA)
and European Medicines Evaluation Force (EMEA) for the duration of the treatment of IPF.
Take InterMune
InterMune is a biotechnology company focused on the research,
development and commercialization of innovative therapies in pulmonology
and hepatology. InterMune has a pipeline portfolio addressing idiopathic
pulmonary fibrosis (IPF) and hepatitis C virus (HCV) infections. The
pulmonology portfolio includes two Phase III programs evaluating thinkable
therapeutic candidates for treatment of patients with IPF: the INSPIRE
trial is evaluating Actimmune(R) and the CAPACITY program is evaluating
pirfenidone. The hepatology portfolio includes the lead HCV protease
inhibitor compound, ITMN-191, formerly referred to as ITMN B, a
number two-formation HCV protease inhibitor program, and a probing program
evaluating a new end in hepatology. For additional word anent
InterMune and its R&D passage, please visit http://www.intermune.com/.
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InterMune, Inc.
http://www.intermune.com/