Agennix Announces Issuance of European Patent Covering Use of Talactoferrin to Treat Cancer

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Patents, Copyright & Trademarks

Planegg/Munich (Germany), Princeton, NJ and Houston, TX, August 10, 2011 (euro
adhoc) - Agennix AG (Frankfurt Stock Exchange (Prime Standard): AGX) today
announced that the European Patent Office has issued patent number 1507554,
entitled, "Lactoferrin in the treatment of malignant neoplasms and other
hyperproliferative diseases," covering the use of oral human lactoferrins,
including talactoferrin, to treat cancer.  It also covers the use of
talactoferrin in combination with other therapies, including chemotherapy,
immunotherapy, radiation therapy and other treatments. The patent has a term
until 2023.

Torsten Hombeck, Ph.D., Spokesperson of the Management Board and Chief Financial
Officer, said: "This patent further strengthens our intellectual property
position for talactoferrin in the area of oncology.  This European patent
provides broad protection for talactoferrin in this key market, as it covers the
use of human lactoferrin for oral administration, used alone or in combination
with other therapies, for the treatment of all cancer types.  We also have
cancer use patents that were recently issued in the U.S. and Japan, two of the
other major markets for talactoferrin, that provide protection until 2025 and
2023, respectively, and include coverage for our lead indication, non-small cell
lung cancer."

About talactoferrin
Talactoferrin is an oral immunotherapy that is being studied for the treatment
of cancer and severe sepsis. Talactoferrin has demonstrated promising activity
in randomized, double-blind, placebo-controlled Phase II studies in non-small
cell lung cancer (NSCLC) and in severe sepsis. Two Phase III trials with
talactoferrin in NSCLC are ongoing. The FORTIS-M trial, which completed
enrollment in March 2011, is evaluating talactoferrin in NSCLC patients whose
disease has progressed following two or more prior treatment regimens.  A second
Phase III trial - FORTIS-C - is evaluating talactoferrin in combination with the
standard chemotherapy regimen, carboplatin/paclitaxel, in first-line NSCLC
patients.  NSCLC is one of the most common types of cancer worldwide and the
most frequent cause of cancer death.  Agennix is also developing talactoferrin
for the treatment of severe sepsis and has initiated a Phase II/III trial,
called the OASIS trial, in that indication.  Talactoferrin has been shown to be
very well tolerated in these patient populations.  

About Agennix
Agennix AG is a publicly listed biopharmaceutical company that is focused on the
development of novel therapies that have the potential to substantially improve
the length and quality of life of critically ill patients in areas of major
unmet medical need. The Company's most advanced program is talactoferrin, an
oral immunotherapy that has demonstrated activity in randomized, double-blind,
placebo-controlled Phase II studies in non-small cell lung cancer and in severe
sepsis. Talactoferrin is currently in Phase III clinical trials in non-small
cell lung cancer, and a Phase II/III trial with talactoferrin in severe sepsis
is underway. Other clinical development programs include RGB-286638, a
multi-targeted kinase inhibitor in Phase I testing, and a topical gel form of
talactoferrin for diabetic foot ulcers. Agennix's registered seat is in
Heidelberg, Germany. The Company has three sites of operation: Planegg/Munich,
Germany; Princeton, New Jersey and Houston, Texas. For additional information,
please visit the Agennix Web site at

This press release contains forward-looking statements, which express the
current beliefs and expectations of the management of Agennix AG. Such
statements are based on current expectations and are subject to risks and
uncertainties, many of which are beyond our control, that could cause future
results, performance or achievements to differ significantly from the results,
performance or achievements expressed or implied by such forward-looking
statements. Actual results could differ materially depending on a number of
factors, and we caution investors not to place undue reliance on the
forward-looking statements contained in this press release. Even if the results
from our later stage trials with talactoferrin, including the ongoing FORTIS-M
trial in non-small cell lung cancer, are considered positive, there can be no
guarantee that they will be sufficient to gain marketing approval in the United
States or any other country, and regulatory authorities may require additional
information, data and/or further pre-clinical or clinical studies to support
approval.  In such event, there can be no guarantee that the Company will have
or be able to obtain the financial resources to conduct any such additional
studies or that such studies will yield results sufficient for approval. 
Forward-looking statements speak only as of the date on which they are made and
Agennix undertakes no obligation to update these forward-looking statements,
even if new information becomes available in the future.
Agennix? is a trademark of the Agennix group.

Further inquiry note:
Barbara Mueller
Manager, Investor Relations & Corporate Communications 		
Phone: +49 (0)89 8565 2693
In the U.S.: Laurie Doyle		
Senior Director, Investor Relations & Corporate Communications		
Phone: +1 609 524 5884
Additional media contact for Europe:	
MC Services AG	
Raimund Gabriel	
Phone: +49 (0) 89 210 228 0
Additional investor contact for Europe:	
Trout International LLC	
Lauren Williams, Vice President	
Phone: +44 207 936 9325

end of announcement                               euro adhoc 

company:     AGENNIX AG
             Im Neuenheimer Feld 515
             D-69120 Heidelberg
phone:       +49 89 8565 2693
FAX:         +49 89 8565 2610
sector:      Pharmaceuticals
ISIN:        DE000A1A6XX4
indexes:     CDAX, Prime All Share, Technology All Share
stockmarkets: regulated dealing/prime standard: Frankfurt, free trade: Berlin,
             Hamburg, Düsseldorf, Hannover, München 
language:   English

Weitere Meldungen: AGENNIX AG

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