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Epigenomics AG Announces Q1 2015 Financial Results and Reports on Operational Highlights

Epigenomics AG / Key word(s): Quarter Results/Quarter Results

2015-05-12 / 08:30


Press release

Epigenomics AG Announces Q1 2015 Financial Results and Reports on Operational Highlights

Epigenomics reaches 99.5% adherence for Epi proColon(R) in the ADMIT Trial

BioChain starts to commercialize Epi proColon(R) in China

Epigenomics receives EUR 2.8 million grant from European Commission to support development of Epi proLung(R)

Solid financial position; liquidity at the end of period EUR 6.4 million; Up to EUR 5 million rights issue underway

Berlin (Germany) and Germantown, MD (U.S.A.), May12, 2015 – Epigenomics AG (Frankfurt Prime Standard: ECX, OTCQX: EPGNY), the German-American cancer molecular diagnostics company today announced its financial results for the first quarter of 2015 ending March 31.

“Our activities in the first quarter 2015 very much focused on completion of the ADMIT trial (ADherence to Minimally Invasive Testing – NCT02251782) requested by the U.S. Food and Drug Administration (FDA) as part of our pre-market approval (PMA) application for Epi proColon(R). With an adherence rate of nearly 100% to colorectal cancer (CRC) screening using Epi proColon(R) we remain convinced that the study results will support our PMA application and plan to submit the data to the FDA over the next few weeks,” said Dr. Thomas Taapken, CEO/CFO of Epigenomics AG. “We are now also starting to shift research and development resources from Epi proColon(R) towards future product opportunities, most notably the development of a blood-based lung cancer test.”

Q1 2015 Financial Results

– Q1 2015 revenue slightly decreased to EUR 367 thousand (Q1 2014: EUR 407 thousand); thereof, product revenue decreased by 21% year-on-year (from EUR 215 thousand to EUR 169 thousand), however, initial product orders for the Chinese market have been received for the following quarters and will lead to higher revenue in the second half of the year.

– Q1 2015 operating costs increased to EUR 3.7 million from EUR 2.5 million in Q1 2014. This increase was completely in line with the Company’s forecast and primarily attributable to higher R&D costs of EUR 2.2 million (Q1 2014: EUR 1.3 million) due to conducting the ADMIT trial and an increase in provisions relating to the phantom stock programs. SG&A costs increased to EUR 1.3 million (Q1 2014: EUR 1.0 million) mainly attributable to an increase in provisions relating to the phantom stock programs and legal and consulting expenses with regard to the Company’s targeted U.S. market entry.

– In line with the increase in operating costs, EBIT for Q1 2015 amounted to EUR -3.2 million (Q1 2014: EUR -2.0 million) and net loss for the period to EUR 3.2 million (Q1 2014: EUR 2.2 million). Due to the increased number of shares outstanding at the end of Q1 2015, net loss per share increased only slightly to EUR 0.20 (Q1 2014: EUR 0.17).

– Cash outflow from operating activities was EUR 2.2 million in Q1 2015 – an increase of EUR 0.7 million compared to Q1 2014 (EUR 1.5 million) which was mainly attributable to the ADMIT trial and to building up product inventory for expected product demand in the months to come. Cash inflow from financing activities amounted to EUR 1.0 million (Q1 2014: EUR 1.9 million) due to the conversion of two convertible notes by their holders.

– Liquid assets amounted to EUR 6.4 million at the reporting date (Dec 31, 2014: EUR 7.5 million).

Summary of Operational Highlights

Epigenomics reaches 99.5% adherence for Epi proColon(R) in the ADMIT trial (after period-end): Results from the ADMIT trial, published last week (for detailed results reference is made to the press release dated May 8, 2015), demonstrated a 99.5% rate of adherence to CRC screening using Epi proColon(R), while the fecal immunochemical test (FIT) showed an adherence rate of 88.1%. Seeing adherence with Epi proColon(R) approaching 100% clearly confirms the Company’s assumption that blood-based CRC screening has the potential to significantly lower the barrier for patients that have been historically non-compliant to participate in CRC screening programs.

Marketing start of Epi proColon(R) in China: Since the approval of Epi proColon(R) in China, Epigenomics has been assisting its partner BioChain in their efforts to work with the provincial governments to secure adequate pricing and reimbursement decisions to support the market adoption and to secure the commercial success of its innovative blood-based test for early detection of CRC in China. Epigenomics has received initial product orders post approval for delivery and expects a ramp-up in sales during the second half of the year.

Strengthening manufacturing capabilities: To secure the commercialization progress of its main product Epi proColon(R), the Company has established a second source for product manufacturing, which mitigates potential supply chain risks. In addition, the Company is evaluating further steps to shorten manufacturing lead times and reduce costs. Also, the company is building product inventory in preparation of the launch of Epi proColon(R) in the US and China.

European Commission grants EUR 2.8 million to Epigenomics for development of blood-based Epi proLung(R) test (after period-end): Epigenomics is eligible to receive an EU grant under the industrial leadership of the Horizon 2020 program. The grant with a total fund volume of up to EUR 2.8 million is intended to fund the clinical research to validate Epigenomics’ proprietary lung cancer biomarker SHOX2 with the goal to develop a CE-marked product for the detection of lung cancer in blood plasma under the new in-vitro diagnostic directive.

Epigenomics announced Capital Increase of up to EUR 5 million (after period-end): To strengthen the Company’s liquidity, to finance certain market introductory measures for Epi proColon(R) in the U.S., to strengthen its manufacturing capabilities as well as to build product inventory, Epigenomics has announced a rights issue of up to EUR 5 million. The subscription period will start on May 13, 2015, and will end on May 27, 2015.

Outlook 2015

– The Company confirms its prognosis for fiscal 2015 as outlined in the Group Management Report of the 2014 Annual Report. However, if the announced rights issue is successful, this could have a positive impact on the Company’s financial position in the remainder of 2015 and on the cash reach projections. All business projections for 2015 are still based on the approval of Epi proColon(R) as an IVD product in the U.S. market around mid-year and the generation of first revenues from Q3 2015 on.

Further Information

The full Q1 2015 Financial Report can be obtained from Epigenomics’ website at:

https://www.epigenomics.com/en/news-investors/investors/financial-reports/2015.html

– Ends –

About Epigenomics

Epigenomics (www.epigenomics.com) is a molecular diagnostics company developing and commercializing innovative products for cancer. The Company’s products enable doctors to diagnose cancer earlier and more accurately, leading to improved outcomes for patients. Epigenomics’ lead product, Epi proColon(R), is a blood-based test for the early detection of colorectal cancer, which is currently marketed in Europe, has received approval by the Chinese Food and Drug Administration for China and is under regulatory review by the U.S. Food and Drug Administration (FDA). Additionally, the Company markets its tissue assay for use in lung cancer diagnosis, Epi proLung(R), in Europe. The Company’s technology and products have been validated through multiple partnerships with leading global diagnostic companies and testing laboratories. Epigenomics is an international company with operations in Europe and the U.S.A.

Contact Epigenomics AG

Antje Zeise, Manager IR | PR
Epigenomics AG
Geneststraße 5
10829 Berlin
Phone +49 (0) 30 24345 386
ir@epigenomics.com
www.epigenomics.com

For US press inquiries:

Epigenomics, Inc.
20271 Goldenrod Lane, Suite 2027
Germantown, Maryland 20876
pr@epigenomics.com

Epigenomics legal disclaimer
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 by Epigenomics in the United States or Canada. The analytical and clinical performance characteristics of any Epigenomics product based on this technology which may be sold at some future time in the U.S. have not been established.

 


2015-05-12 Dissemination of a Corporate News, transmitted by DGAP – a service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.

The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.
Media archive at www.dgap-medientreff.de and www.dgap.de



356079  2015-05-12 
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Ad Hoc Announcement pursuant to Sec. 15 WpHG (German Securities Trading Act): Epigenomics AG Announces Capital Increase up to EUR 5M

Epigenomics AG  / Key word(s): Capital Increase/Miscellaneous

11.05.2015 08:38

Dissemination of an Ad hoc announcement according to § 15 WpHG, transmitted
by DGAP - a service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.

---------------------------------------------------------------------------

Not for distribution in the United States of America

Berlin, Germany, May 11, 2015 - Today the Executive Board of Epigenomics
AG, Berlin, Germany (Frankfurt Prime Standard: ECX; ISIN: DE000A11QW50),
with the approval of the Supervisory Board, resolved to partially exercise
its authorization under the Company's Authorized Capital 2014/II and to
increase the Company's issued share capital against cash contributions from
currently EUR 16,092,197.00 by up to EUR 976,562 up to EUR 17,068,759 by
issuing up to 976,562 new ordinary registered shares with no-par value,
each such share representing a notional nominal amount of the issued share
capital of EUR 1.00 per share. The new shares will be issued at a
subscription price of EUR 5.12 per new share and will carry full dividend
rights as from January 1, 2015. The capital increase is conducted by way of
rights issue. The new shares will be offered to the Company's shareholders
at a subscription ratio of 33:2, i.e. the Company's shareholders may
subscribe for each 33 existing shares 2 new shares. In addition, the
shareholders will be offered the possibility to subscribe for additional
shares (oversubscription).

The subscription offer is expected to be published on the Company's website
(www.epigenomics.com) and in the German Federal Gazette (Bundesanzeiger) on
May 13, 2015. The subscription period for the Company's shareholders is
expected to begin on May 13, 2015 and to end on May 27, 2015 (in each case
including such dates). No trading in subscription rights will be organized.

Shares not subscribed for by shareholders might subsequently be offered in
a private placement to institutional investors subject to selling
restrictions as may be applicable in certain jurisdictions. The actual
number of new shares eventually issued in, and the final amount of, the
capital increase is determined following the end of the subscription period
and the take up under the private placement; it will be announced by a
separate ad-hoc announcement.

The capital increase is structured in a manner that the gross proceeds
generated by it will at a maximum be equal to an amount just short of EUR
5,000,000.00, but will not reach that amount, so that the capital increase
does not require a prospectus under German law. The amount of the gross
proceeds actually generated depends on the number of new shares eventually
subscribed for or taken up under the private placement and may therefore
fall more or less short of the envisaged maximum amount.

Epigenomics AG intends to use the net proceeds from the offering to finance
certain market introductory measures for Epi proColon(R) in the US, to
strengthen its manufacturing capabilities as well as to build product
inventory and lastly to finance its current business operations.

- End of Ad hoc -

Disclaimer

This publication is not an offer of any securities for sale or a
solicitation of an offer to purchase any securities.

This document is not an offer of securities for sale or a solicitation of
an offer to purchase securities in the United States of America. The shares
of Epigenomics AG (the "Shares") have not been registered under the U.S.
Securities Act of 1933, as amended (the "Securities Act"), and may not be
offered or sold in the United States unless registered under the Securities
Act or pursuant to an exemption from such registration. There will be no
public offering of the Shares in the United States and the Shares will not
be registered under the Securities Act.

Contact:

Epigenomics AG    

Antje Zeise CIRO
Manager IR | PR 
Epigenomics AG 
Phone: +49 (0) 30 24345 386 
ir@epigenomics.com
www.epigenomics.com


11.05.2015 The DGAP Distribution Services include Regulatory Announcements,
Financial/Corporate News and Press Releases.
Media archive at www.dgap-medientreff.de and www.dgap.de

---------------------------------------------------------------------------
 
Language:     English
Company:      Epigenomics AG
              Geneststraße 5
              10829 Berlin
              Germany
Phone:        +49 30 24345-0
Fax:          +49 30 24345-555
E-mail:       ir@epigenomics.com
Internet:     www.epigenomics.com
ISIN:         DE000A11QW50
WKN:          A11QW5
Listed:       Regulated Market in Frankfurt (Prime Standard); Regulated
              Unofficial Market in Berlin, Dusseldorf, Munich, Stuttgart
 
End of Announcement                             DGAP News-Service
 
---------------------------------------------------------------------------

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Epigenomics Reaches 99.5 % Adherence for Epi proColon(R) in ADMIT Study

Epigenomics AG / Key word(s): Study/Study results

2015-05-08 / 09:06


Epigenomics Reaches 99.5 % Adherence for Epi proColon(R) in ADMIT Study

Berlin, Germany, May 8, 2015 – Epigenomics AG (Frankfurt Prime Standard: ECX; ISIN: DE000A11QW50) announces results from the ADMIT trial (ADherence to Minimally Invasive Testing – NCT02251782) for its non-invasive blood-based test for colorectal cancer (CRC) screening, Epi proColon(R). The study demonstrated a 99.5% rate of adherence to CRC screening using Epi proColon(R), while the fecal immunochemical test (FIT) showed an adherence rate of 88.1%. These numbers contrast to a baseline adherence to standard of care CRC screening of less than 25%, as measured in a passive control arm in which previously non-compliant patients were offered CRC screening tests (FIT or colonoscopy) as part of their standard of care.

Adherence to Epi proColon(R) was significantly greater than adherence to FIT, with an observed difference of 11.4% (p<0.0001).

The study was designed to determine whether the adherence to Epi proColon(R) was significantly greater than to FIT plus a margin of 8.2%. This margin was determined before the study based on a projected FIT adherence rate. While adherence to Epi proColon(R) ultimately was higher than the FIT adherence plus 8.2%, the comparison fell just short of statistical significance (p=0.059). However, given the difference in the observed FIT adherence rate in the study from the projected one, demonstrating an adherence to Epi proColon(R) equaling the FIT adherence rate plus a margin of 3.2% would have been sufficient to prove superiority. In this scenario, the observed difference in adherence (11.4%) met statistical significance (p<0.0001).

“We are convinced that these study results will support our pre-market approval (PMA) application for Epi proColon(R). Seeing adherence with Epi proColon(R) approaching 100% clearly confirms our assumption that blood-based CRC screening has the potential to significantly lower the barrier for patients that have been historically non-compliant to participate in CRC screening programs,” said Dr. Thomas Taapken, CEO of Epigenomics. “We plan to submit the data as part of our PMA application and further discuss the study results with the U.S. Food and Drug Administration (FDA) over the next few weeks.”

The ADMIT trial was requested by the FDA in the context of Epigenomics’ PMA application for Epi proColon(R).

The study was originally designed to investigate CRC screening participation for average risk, screening eligible study subjects that were historically non-compliant to offered guideline-recommended screening methods (colonoscopy or FIT testing) and included 413 eligible subjects identified by Epigenomics’ clinical trial partners, Kaiser Permanente and Geisinger Health Systems. Study subjects were randomized to either a FIT test kit for home use or a blood draw for the Epi proColon(R) test. Rates of adherence were compared between those that accepted and completed the blood test and those that accepted and completed the FIT test.

An observational secondary objective of the study aims to demonstrate the number of patients who completed colonoscopy after positive test results with Epi proColon(R) or FIT. This data will be reported to the FDA once the study is formally completed within the next few weeks, i.e. up to six weeks after the last positive test result of a study subject was obtained.

Further Information

For further information please refer to the press release issued today by Epigenomics AG at www.epigenomics.com.

Conference call for press and analysts

Epigenomics’ management will host a conference call at 3pm CET/9 am ET today, Friday 8th May 2015.

The dial-in numbers for the conference call are:

Dial-in number (within Germany): +49 69 247 501 895

Dial-in number (within the UK): +44 203 367 92 16

Dial-in number (within the U.S.): +1 408 9169 838

Participants are kindly requested to dial in 10 minutes prior to the start of the call.

An audio replay of the conference call will be provided on Epigenomics’ website subsequently: https://www.epigenomics.com/en/news-investors.html

About Epigenomics

Epigenomics (www.epigenomics.com) is a molecular diagnostics company developing and commercializing innovative products for cancer. The Company’s products enable doctors to diagnose cancer earlier and more accurately, leading to improved outcomes for patients. Epigenomics’ lead product, Epi proColon(R), is a blood-based test for the early detection of colorectal cancer, which is currently marketed in Europe, has received approval by the Chinese Food and Drug Administration for China and is under regulatory review by the U.S. Food and Drug Administration (FDA). Additionally, the Company markets its tissue assay for use in lung cancer diagnosis, Epi proLung(R), in Europe. The Company’s technology and products have been validated through multiple partnerships with leading global diagnostic companies and testing laboratories. Epigenomics is an international company with operations in Europe and the U.S.A.

Contact Epigenomics AG

Antje Zeise, Manager IR | PR
Epigenomics AG
Geneststraße 5
10829 Berlin
Phone +49 (0) 30 24345 386
ir@epigenomics.com
www.epigenomics.com

For US press inquiries:

Epigenomics, Inc.
20271 Goldenrod Lane, Suite 2027
Germantown, Maryland 20876
pr@epigenomics.com

Epigenomics legal disclaimer

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 by Epigenomics in the United States or Canada. The analytical and clinical performance characteristics of any Epigenomics product based on this technology which may be sold at some future time in the U.S. have not been established.


2015-05-08 Dissemination of a Corporate News, transmitted by DGAP – a service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.

The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.
Media archive at www.dgap-medientreff.de and www.dgap.de



354845  2015-05-08 
Read more

Epigenomics Reaches 99.5 % Adherence for Epi proColon(R) in ADMIT Study

Epigenomics AG  / Key word(s): Study/Study results

08.05.2015 09:04

Dissemination of an Ad hoc announcement according to § 15 WpHG, transmitted
by DGAP - a service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.

---------------------------------------------------------------------------

Epigenomics Reaches 99.5 % Adherence for Epi proColon(R) in ADMIT Study

Berlin, Germany, May 8, 2015 - Epigenomics AG (Frankfurt Prime Standard:
ECX; ISIN: DE000A11QW50) announces results from the ADMIT trial (ADherence
to Minimally Invasive Testing - NCT02251782) for its non-invasive
blood-based test for colorectal cancer (CRC) screening, Epi proColon(R).
The study demonstrated a 99.5% rate of adherence to CRC screening using Epi
proColon(R), while the fecal immunochemical test (FIT) showed an adherence
rate of 88.1%. These numbers contrast to a baseline adherence to standard
of care CRC screening of less than 25%, as measured in a passive control
arm in which previously non-compliant patients were offered CRC screening
tests (FIT or colonoscopy) as part of their standard of care.

Adherence to Epi proColon(R) was significantly greater than adherence to
FIT, with an observed difference of 11.4% (p< 0.0001). 

The study was designed to determine whether the adherence to Epi
proColon(R) was significantly greater than to FIT plus a margin of 8.2%.
This margin was determined before the study based on a projected FIT
adherence rate. While adherence to Epi proColon(R) ultimately was higher
than the FIT adherence plus 8.2%, the comparison fell just short of
statistical significance (p=0.059). However, given the difference in the
observed FIT adherence rate in the study from the projected one,
demonstrating an adherence to Epi proColon(R) equaling the FIT adherence
rate plus a margin of 3.2% would have been sufficient to prove superiority.
In this scenario, the observed difference in adherence (11.4%) met
statistical significance (p< 0.0001).

Seeing adherence with Epi proColon approaching 100% clearly confirms
Epigenomics' assumption that blood-based CRC screening has the potential to
significantly lower the barrier for patients that have been historically
non-compliant to participate in CRC screening programs. The Company is
convinced that the study results support its pre-market approval (PMA)
application for Epi proColon(R) and plans to submit the data and further
discuss the study results with the U.S. Food and Drug Administration (FDA)
over the next few weeks.

The ADMIT trial was requested by the FDA in the context of Epigenomics' PMA
application for Epi proColon(R).

The study was originally designed to investigate CRC screening
participation for average risk, screening eligible study subjects that were
historically non-compliant to offered guideline-recommended screening
methods (colonoscopy or FIT testing) and included 413 eligible subjects
identified by Epigenomics' clinical trial partners, Kaiser Permanente and
Geisinger Health Systems. Study subjects were randomized to either a FIT
test kit for home use or a blood draw for the Epi proColon(R) test. Rates
of adherence were compared between those that accepted and completed the
blood test and those that accepted and completed the FIT test.

An observational secondary objective of the study aims to demonstrate the
number of patients who completed colonoscopy after positive test results
with Epi proColon(R) or FIT. This data will be reported to the FDA once the
study is formally completed within the next few weeks, i.e. up to six weeks
after the last positive test result of a study subject was obtained.


---------------------------------------------------------------------------

Information and Explaination of the Issuer to this News:

Further Information

For further information please refer to the press release issued today by
Epigenomics AG at www.epigenomics.com.

Conference call for press and analysts

Epigenomics' management will host a conference call at 3pm CET/9 am ET
today, Friday 8th May 2015.

The dial-in numbers for the conference call are:
Dial-in number (within Germany): +49 69 247 501 895
Dial-in number (within the UK): +44 203 367 92 16
Dial-in number (within the U.S.): +1 408 9169 838

Participants are kindly requested to dial in 10 minutes prior to the start
of the call.

An audio replay of the conference call will be provided on Epigenomics'
website subsequently: https://www.epigenomics.com/en/news-investors.html

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 by Epigenomics in the
United States or Canada. The analytical and clinical performance
characteristics of any Epigenomics product based on this technology, which
may be sold at some future time in the U.S. have not been established.

Contact:
Epigenomics AG    
Antje Zeise CIRO
Manager IR | PR 
Epigenomics AG 
Phone: +49 (0) 30 24345 386 
ir@epigenomics.com
www.epigenomics.com

08.05.2015 The DGAP Distribution Services include Regulatory Announcements,
Financial/Corporate News and Press Releases.
Media archive at www.dgap-medientreff.de and www.dgap.de

---------------------------------------------------------------------------
 
Language:     English
Company:      Epigenomics AG
              Geneststraße 5
              10829 Berlin
              Germany
Phone:        +49 30 24345-0
Fax:          +49 30 24345-555
E-mail:       ir@epigenomics.com
Internet:     www.epigenomics.com
ISIN:         DE000A11QW50
WKN:          A11QW5
Listed:       Regulated Market in Frankfurt (Prime Standard); Regulated
              Unofficial Market in Berlin, Dusseldorf, Munich, Stuttgart
 
End of Announcement                             DGAP News-Service
 
---------------------------------------------------------------------------

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Epigenomics AG: Veröffentlichung der Gesamtzahl der Stimmrechte nach § 26a WpHG mit dem Ziel der europaweiten Verbreitung

Epigenomics AG  / Veröffentlichung der Gesamtzahl der Stimmrechte

30.04.2015 11:30

Veröffentlichung der Gesamtzahl der Stimmrechte nach  § 26a WpHG, übermittelt durch DGAP - ein Service der EQS Group AG.
Für den Inhalt der Mitteilung ist der Emittent verantwortlich.

---------------------------------------------------------------------------

Hiermit teilt die Epigenomics AG mit, dass die Gesamtzahl der Stimmrechte
am Ende des Monats April 2015 insgesamt 16092197 Stimmrechte beträgt.



30.04.2015 Die DGAP Distributionsservices umfassen gesetzliche 
Meldepflichten, Corporate News/Finanznachrichten und Pressemitteilungen. 
DGAP-Medienarchive unter www.dgap-medientreff.de und www.dgap.de

---------------------------------------------------------------------------
 
Sprache:      Deutsch
Unternehmen:  Epigenomics AG
              Geneststraße 5
              10829 Berlin
              Deutschland
Internet:     www.epigenomics.com
 
Ende der Mitteilung                             DGAP News-Service
 
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Epigenomics receives EUR 2.8m grant for Validation of Lung Cancer Biomarkers in Blood Plasma

Epigenomics AG / Key word(s): Miscellaneous/Miscellaneous

2015-04-29 / 09:30


Press release

Epigenomics receives EUR 2.8m grant for Validation of Lung Cancer Biomarkers in Blood Plasma

Berlin (Germany) and Germantown, MD (U.S.A.), April 29, 2015 – Epigenomics AG (Frankfurt Prime Standard: ECX, OTCQX: EPGNY), the German-American cancer molecular diagnostics company, today announced that the Company will receive an EU grant under the industrial leadership Horizon 2020 research and innovation program for SME (Small and Medium-Sized Enterprises). The grant duration is expected to be 24 months with a total fund volume of up to EUR 2.77 million.

The grant will fund the clinical research to validate Epigenomics’ proprietary lung cancer biomarkers with the goal to develop a CE-marked product for the detection of lung cancer in blood plasma under the new in-vitro diagnostic directive.

“We are proud, that our lung cancer grant application has received the favor of the Horizon 2020 program”, said Dr. Uwe Staub, COO of Epigenomics. “With our Epi proLung(R) test we have already proven that new and innovative diagnostic tests can make a difference in the detection of lung cancer. With this new project, we will clinically validate a novel CE-marked diagnostic product that can detect lung cancer in blood plasma at an early stage and has a variety of possible future clinical applications in the diagnosis of lung cancer.”

The EU commission informed Epigenomics that the grant proposal has been favorably evaluated and that the agency wishes to proceed with the grant agreement. In a next step the grant agreement preparation and the internal completion of the formal selection process will be concluded.

About Horizon 2020

Horizon 2020 is the EU Framework Program for Research and Innovation and the largest EU program ever in this field with nearly EUR 80 billion of funding available over 7 years (2014 to 2020). It represents a flagship initiative aimed at securing global competitiveness, economic growth and job creation in Europe through the promotion of innovation and research. Horizon 2020 is divided into three sections. The pillar “industrial leadership” aims to speed up development of the technologies and innovations that will underpin tomorrow’s businesses and help innovative European SMEs to grow into world-leading companies.

About Epigenomics

Epigenomics (www.epigenomics.com) is a molecular diagnostics company developing and commercializing innovative products for cancer. The Company’s products enable doctors to diagnose cancer earlier and more accurately, leading to improved outcomes for patients. Epigenomics’ lead product, Epi proColon(R), is a blood-based test for the early detection of colorectal cancer, which is currently marketed in Europe, has received approval by the Chinese Food and Drug Administration for China and is under regulatory review by the U.S. Food and Drug Administration (FDA). Additionally, the Company markets its tissue assay for use in lung cancer diagnosis, Epi proLung(R), in Europe. The Company’s technology and products have been validated through multiple partnerships with leading global diagnostic companies and testing laboratories. Epigenomics is an international company with operations in Europe and the U.S.A.

Contact Epigenomics AG

Antje Zeise, Manager IR | PR
Epigenomics AG
Geneststraße 5
10829 Berlin
Phone +49 (0) 30 24345 386
ir@epigenomics.com
www.epigenomics.com

For US press inquiries:

Epigenomics, Inc.
20271 Goldenrod Lane, Suite 2027
Germantown, Maryland 20876
pr@epigenomics.com

Epigenomics legal disclaimer

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 by Epigenomics in the United States or Canada. The analytical and clinical performance characteristics of any Epigenomics product based on this technology which may be sold at some future time in the U.S. have not been established.

 


2015-04-29 Dissemination of a Corporate News, transmitted by DGAP – a service of EQS Group AG.
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