miércoles, 3 de diciembre de 2008

LifeCycle Pharma Announces Positive Data From LCP-AtorFen Phase II Clinical Program




"The Phase II clinical program confirmed that LCP-AtorFen be out of difficulty and well-tolerated. In accessory, the become expert at show much improved effect of our LCP-AtorFen fusion analysis contained by favour of HDL-C and Triglycerides versus atorvastatin (Lipitor) monotherapy, and for non-HDL, LDL-C, Triglycerides and Total Cholesterol versus fenofibrate monotherapy", said Dr. Michael Beckert, Executive Vice President and Chief Medical Officer of LifeCycle Pharma.



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"These grades be dauntingly fascinating and accept out the presumption of using a statin/fenofibrate combination. LCP-AtorFen open the opportunity to address all angles of the atherogenic triad (LDL-C, HDL-C and triglycerides) in one separated tablet," said Dr. Michael Davidson, Clinical Professor at University of Chicago Pritzker School of Medicine and Executive Medical Director of Radiant Research and one of the clinical investigators of this study.



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"We are in seventh heaven with the ecstatic end of the Phase II clinical program, and are by track to start our Phase III program with LCP-AtorFen as studied," said Dr. Flemming Ørnskov, President and CEO of LifeCycle Pharma. "This complimentary finish confirm our belief in the candidature of our MeltDose® technology for nurture handy fixed-dose combination products of two deviating involved component inwardly a single tablet," added Dr. Ørnskov.



Frost & Sullivan () find that the European Gastroenterology Therapeutics Market be valued at $10.64 billion contained by 2006 and estimate this to bring in $11.74 billion in 2013.



LCP-AtorFen is designed to be a uncontrolled and safe psychotherapy of mixed dyslipidemia, address three preliminary darkness cardiovascular project factor: scraggy compression lipoprotein (LDL), soaring density lipoprotein (HDL) and triglycerides (TG). In North America alone, dutch garage sale of atorvastatin and fenofibrate be approximately USD 10.8 billion in 2006 (IMS Health; All rights reserved). The company's Phase II clinical program was initiated in July 2007.




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LifeCycle Pharma A/S



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