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Epigenomics AG

EANS-Adhoc: Ad Hoc Announcement Pursuant to §15 WpHG (German Securities Trading Act) Epigenomics AG Releases Preliminary PRESEPT Study Data

  ad-hoc disclosure pursuant to section 15 of the WpHG transmitted by euro
  adhoc with the aim of a Europe-wide distribution. The issuer is solely
  responsible for the content of this announcement.
Company Information/Molecular diagnostics
15.01.2010
Berlin, January 15, 2010 - Epigenomics AG (ISIN: DE000A0BVT96), a 
cancer molecular diagnostics company, informs on preliminary data 
from the prospective multi-center clinical PRESEPT Colorectal Cancer 
Screening Study (clinicaltrials.gov; identifier: NCT00855348) 
sponsored by the company. The primary study objective is to 
demonstrate that the Septin9 biomarker satisfies the requirements for
noninvasive screening tests set forth in current joint guidelines by 
the American Cancer Society, the US Multi-Society Task Force on 
Colorectal Cancer, and the American College of Radiology.(Ref. 1) The
results of this preliminary data analysis were reported by Timothy R.
Church, Ph.D., University of Minnesota, Minneapolis, MN, U.S.A., 
Principle Investigator of the PRESEPT Study on behalf of the PRESEPT 
Clinical Study Steering Committee, chaired by Professor David 
Ransohoff, M.D. University of North Carolina School of Medicine, 
Chapel Hill, NC, U.S.A.
This preliminary analysis indicates that two of the three testing 
laboratories performing the Septin9 testing on blood plasma samples 
from PRESEPT Study subjects achieved cancer detection rates of 62.5% 
each, that were within expectations from previously published 
clinical studies (Refs 2-4) taking into account the higher proportion
of early stage cancers in the PRESEPT Study cohort. The third 
laboratory reported a cancer detection rate of 28% deviating from 
findings in the other PRESEPT Study testing laboratories and all 
previous studies. The overall cancer detection rate based on results 
from all three laboratories combined added up to 50%. Specificity as 
measured on colonoscopy verified subjects without any apparent colon 
disease was at 91% confirming the high specificity rates seen in 
previous clinical studies.
The Clinical Study Steering Committee, which includes the Principal 
Investigator representing the independent University of Minnesota 
biostatistics team, charged with analyzing the PRESEPT data, intends 
to conduct a failure investigation to identify the potential causes 
for the outlier results observed in the one of the laboratory before 
reporting final results of the study, that may deviate from the 
reported preliminary results of the study.
Between June 2008 and December 2009, 7,914 average risk, CRC 
screening eligible subjects were enrolled into the PRESEPT Study at 
32 clinical sites, of which 22 sites were located in the U.S. and 10 
sites were located in Germany. This study population contained 50 
confirmed cases of previously unsuspected colorectal cancer that were
identified by screening colonoscopies performed on all study 
participants.
Final and detailed study results will be presented at upcoming 
medical conferences and will also be submitted to a scientific 
journal for peer-review and publication once available.
End of Ad Hoc
Further information
Conference Calls
Epigenomics´ management scheduled conference calls for Monday, 
January 18, 2010 at 15:00 CET (German language) and 17:00 CET/11:00 
am EST (English language) to inform on the preliminary results and 
potential further actions as well as answering questions from 
investors and media. Dial-in details will be published on Epigenomics
website www.epigenomics.com prior to the calls.
References
1. Levin B, et al., Screening and surveillance for the early 
detection of    colorectal cancer and adenomatous polyps, 2008: a 
joint guideline from the    American Cancer Society, the US 
Multi-Society Task Force on Colorectal    Cancer, and the American 
College of Radiology.    Gastroenterology 2008;134(5):1570-95. 2. 
Lofton-Day C, et al. DNA methylation biomarkers for blood-based 
colorectal    cancer screening. Clin Chem. 2008;54(2):414-23. 3. 
Grützmann R, et al. Sensitive detection of colorectal cancer in 
peripheral    blood by mSEPT9 DNA methylation assay. PLoS One. 
2008;3(11):e3759. 4. deVos T, et al. Circulating methylated SEPT9 DNA
in plasma is a biomarker    for colorectal cancer. Clin Chem. 
2009;55(7):1337-46.
Epigenomics legal disclaimers. This communication expressly or 
implicitly contains certain forward-looking statements concerning 
Epigenomics AG and its business. Such statements involve certain 
known and unknown risks, uncertainties and other factors which could 
cause the actual results, financial condition, performance or 
achievements of Epigenomics AG to be materially different from any 
future results, performance or achievements expressed or implied by 
such forward-looking statements. Epigenomics AG is providing this 
communication as of this date and does not undertake to update any 
forward-looking statements contained herein as a result of new 
information, future events or otherwise.
The information contained in this communication does not constitute 
nor imply an offer to sell or transfer any product, and no product 
based on this technology is currently available for sale in the 
United States. The analytical and clinical performance 
characteristics of any product based on this technology which may be 
sold at some future time in the U.S. have not been established.
end of announcement                               euro adhoc

Further inquiry note:

Epigenomics AG
Dr. Achim Plum
Sen. VP Corporate Development
Tel: +49 30 24345 368
achim.plum@epigenomics.com

Branche: Biotechnology
ISIN: DE000A0BVT96
WKN: A0BVT9
Index: Prime All Share, Technology All Share
Börsen: Frankfurt / regulated dealing/prime standard
Berlin / free trade
Hamburg / free trade
Stuttgart / free trade
Düsseldorf / free trade
München / free trade

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