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Cosmo Pharmaceuticals reports highly positive results from the LMW Heparin MMX™ phase IIb trial for Ulcerative Colitis
Lainate, Italy – April 21, 2008 –
Cosmo Pharmaceuticals SpA (SWX:COPN) announced today highly
positive results from a phase IIb trial of Low Molecular Weight
Heparin MMX™ tablet (LMW Heparin MMX™). The results
from the trial show that LMW Heparin MMX™ reached its primary
and secondary end points by inducing superior clinical remission in
patients with active mild to moderate ulcerative colitis and was
well tolerated at once daily dosing.
In the phase IIb randomized, double blind trial more than 120
patients with active left sided mild to moderate ulcerative colitis
were treated in 24 investigator sites in five European countries
using one 210 mg tablet per day for 8 weeks as an add on therapy to
oral mesalazine or other 5-ASA derivatives. Efficacy and
tolerability was measured by comparing the efficacy of LMW Heparin
MMX™ as an add on to mesalazine to a placebo add on to
mesalazine. The primary end point was the number of patients
achieving clinical remission (clinical activity index
(“CAI”) <4) after 8 weeks treatment; the secondary
end point was clinical improvement (by at least 2 points reduction
of the CAI, the endoscopic index (“EI”) and the
histologic score) after 8 weeks treatment.
According to the preliminary reports, at the end of week 8, a
statistically significant higher population of patients achieved
clinical remission in the LMW Heparin MMX™ plus mesalazine
group compared to the placebo plus mesalazine group. The CAI, EI
and histological scores improvement in the LMW Heparin MMX™
group was also statistically significantly higher than in the other
group.
Mauro Ajani, CEO of Cosmo Pharmaceuticals, commented:
“This is very encouraging news for us and for patients. We
had no serious adverse events, the drug was well tolerated and the
efficacy of the drug has been shown to be excellent. More
importantly, the high histologic remission rate gives room to
believe that LMW Heparin MMX™ could be a disease modifying
drug. This all allows us to consider the full range of options
including the potential treatment of patients with moderate to
severe forms of inflammatory bowel diseases. We will now analyze
the data in depth with our scientific advisors in order to
determine how to best position the drug and correspondingly design
the phase III clinical trials both in the USA and
EU.”
It is foreseen to present a fuller report at the research days
in Zurich and London on April 23rd and 24th, 2008.
About Cosmo Pharmaceuticals
Cosmo is a speciality pharma company that aims to become a global
leader in optimised therapies for certain gastrointestinal
diseases. The company’s proprietary clinical development
pipeline specifically addresses innovative treatments for IBD, such
as ulcerative colitis and Crohn’s disease, and colon
infections. Cosmo’s first MMX™ product that has reached
the market is LIALDA™ / MEZAVANT™, a treatment for IBD
that is licensed globally to Giuliani and Shire Pharmaceuticals.
Cosmo’s proprietary MMX™ technology is at the core of
the company’s product pipeline and was developed from its
expertise in formulating and manufacturing gastrointestinal drugs
for international clients at its GMP (Good Manufacturing Practice)
facilities in Lainate, Italy. For further information on Cosmo,
please visit the Company’s website: www.cosmopharmaceuticals.com
Next events
Annual General Meeting April 23, 2008, Milan
Investor and Analyst Day April 23, 2008, Zurich
Registration:
anitta.tuure@irfirm.biz
Investor and Analyst Day April 24, 2008, London
Registration:
emma.thompson@fd.com
Half-year results 2008 July 30, 2008
Contact:
Dr. Chris Tanner, CFO and Head of Investor Relations
Cosmo Pharmaceuticals SpA
Tel: +39 02 9333 7614
Some of the information contained in this press release contains
forward-looking statements. Readers are cautioned that any
such forward-looking statements are not guarantees of future
performance and involve risks and uncertainties, and that actual
results may differ materially from those in the forward-looking
statements as a result of various factors. Cosmo undertakes no
obligation to publicly update or revise any forward-looking
statements.
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