Genaissance Enters into HAP(TM) Technology License Agreement with Sankyo
03 10월 2005 - 9:00PM
PR Newswire (US)
NEW HAVEN, Conn. and TOKYO, Oct. 3 /PRNewswire-FirstCall/ --
Genaissance Pharmaceuticals, Inc. (NASDAQ:GNSC) today announced
that it has entered into an agreement with Sankyo, Co., Ltd.
(TSE:4501), under which the companies will apply Genaissance's
HAP(TM) Technology in conjunction with the focused therapeutic
areas of Sankyo. The goal of the collaboration is to discover
genetic markers related to drug response and then validate these
genetic markers and create a companion diagnostic test that will
guide therapy. Under the terms of the agreement, Genaissance will
receive license and other fees from Sankyo, including fees for
genotyping clinical samples and analyzing the genetic and clinical
data. In addition, Genaissance has certain rights for the
co-development and co-commercialization of a companion genetic
test. "We are very pleased that Sankyo chose Genaissance to help
them integrate pharmacogenomics into drug development," said Kevin
Rakin, President and Chief Executive Officer of Genaissance
Pharmaceuticals. "This is our second agreement with a major
Japanese pharmaceutical company and we hope to see more such
agreements with Japanese companies in the future. We believe this
agreement is an indication that pharmaceutical companies all over
the world are now beginning to use pharmacogenomics as a tool to
improve the success rate of clinical trials and bring innovative
drugs to the market." "We believe that pharmacogenomics offers a
way to develop safer and more effective medicines," said Dr.
Kazuhiko Tanzawa, Executive Officer and Director of R&D
Strategy Department at Sankyo. "This collaboration provides an
excellent opportunity for us to incorporate this technology into
drug development at Sankyo." Patcore, Inc., Genaissance's
representative in Japan, assisted Genaissance in obtaining the
contract. About Sankyo Sankyo Co., Ltd. Of Tokyo, one of Japan's
largest pharmaceutical companies, has a long history of discovering
new classes of drugs, including the statin class of lipid-lowering
drugs. Beginning with its discovery of the first statin,
mevastatin, and the co-discovery of lovastatin, the first statin to
be marketed, Sankyo has been a pioneer in the cardiovascular
disease area. Additionally, Sankyo discovered, developed,
manufactures and markets pravastatin sodium and olmesartan
medoximil, an angiotensin II receptor blocker (ARB). For further
information about Sankyo and its products, log on to
http://www.sankyo.co.jp/english/. About Genaissance Pharmaceuticals
Genaissance Pharmaceuticals, Inc. is developing innovative products
based on its proprietary pharmacogenomic technology and has a
revenue-generating business in DNA and pharmacogenomic products and
services. Genaissance also markets its proprietary FAMILION(TM)
Test, designed to detect mutations responsible for causing Familial
Long QT and Brugada Syndromes, two causes of sudden cardiac death.
The Company's product development strategy is focused on drug
candidates with promising clinical profiles and finding genetic
markers to identify a responsive patient population. This strategy
is designed to enable Genaissance to leverage existing clinical
data and, thus, reduce the costs and risks associated with
traditional drug development and increase the probability of
clinical success and commercialization. The Company's lead
therapeutic product, vilazodone for depression, is in Phase II of
development. For more information on Genaissance, visit the
Company's website at: http://www.genaissance.com/. This press
release contains forward-looking statements as defined in the US
Private Securities Litigation Reform Act of 1995, including
statements about the expected collaboration between Genaissance and
Sankyo, including the discovery of genetic markers related to drug
response and the creation of companion diagnostic tests. Such
statements are subject to certain factors, risks and uncertainties
that may cause actual results, events and performance to differ
materially from those referred to in such statements, including,
but not limited to, the extent to which the technologies under
development between Genaissance and Sankyo are predictive of
clinical outcomes and drug response, acceptance and adoption by the
pharmaceutical industry of the technologies, the amount and timing
of resources that Genaissance and Sankyo devote to their
collaboration, competition from pharmaceutical, biotechnology and
diagnostics companies, the strength of their intellectual property
rights and those risks identified by Genaissance in its Quarterly
Report on Form 10-Q for the quarter ended June 30, 2005, filed with
the Securities and Exchange Commission on August 9, 2005, the
Company's Definitive Proxy Statement dated August 29, 2005, filed
with the Securities and Exchange Commission and in other filings
Genaissance makes with the Securities and Exchange Commission from
time to time. The forward-looking statements contained herein
represent the judgment of Genaissance as of the date of this
release. Genaissance disclaims any obligation to update any
forward-looking statement. DATASOURCE: Genaissance Pharmaceuticals,
Inc. CONTACT: Krishnan Nandabalan, Ph.D., Vice President, Corporate
Development, +1-203-786-3445, , or Carol R. Reed, M.D., Vice
President, Medical Affairs, +1-203-786-3617, , both of Genaissance
Pharmaceuticals, Inc.; or Rhonda Chiger - investors, Rx
Communications, +1-917-322-2569, Web site:
http://www.genaissance.com/ http://www.sankyo.co.jp/english
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