Aida Pharmaceuticals Wins Lawsuit Against Counterfeit Drug Suppliers
February 01 2007 - 8:30AM
PR Newswire (US)
HANGZHOU, China, Feb. 1 /PRNewswire-FirstCall/ -- Aida
Pharmaceuticals, Inc. (OTC:AIDA) (BULLETIN BOARD: AIDA) , one of
mainland China's leading pharmaceutical companies, today announced
the Company has won an infringement lawsuit against four
counterfeit drug suppliers of the transfusion form of Etimicin
Sulfate, Aida Pharmaceuticals' patented antibiotic. The ruling was
handed down by the Intermediate Court of Hainan and demands that
the four companies terminate all manufacturing, marketing and
promotional activities of the counterfeit transfusion form of
Etimicin Sulfate. Additionally, the companies must destroy all
remaining counterfeit products in stock and all marketing material
in circulation, including any collateral on the Internet, issue a
statement of apology to Hainan Aike Pharmaceutical Co., Ltd, one of
Aida's subsidiaries, and compensate Aike US$77,180 (RMB 600,000).
Aida Pharmaceuticals filed the legal action against four
counterfeit drug suppliers at the end of 2005, as the perpetrators'
actions were adversely impacting Aida's financial performance and
undermining the Company's distribution rights. In early 2006, the
defendants applied with the State Intellectual Property Office of
the People's Republic of China (SIPO) for the invalidation of the
Patent of Etimicin Sulfate, under which the Aida Pharmaceuticals'
subsidiary, Hainan Aike Pharmaceutical, was granted the exclusive
production rights of the powder and transfusion forms of Etimicin
Sulfate. SIPO refused the request by the defendant, rejected their
related claims, and reconfirmed the validity of Aike's patent
through 2013. Mr. Jin Biao, Chairman and CEO of Aida stated, "With
approximately 80% of current revenues derived from Etimicin, it is
a very favorable judgment and we are extremely pleased that our
courts are taking decisive and definitive action to punish and
desist the action of these counterfeiters. As we continue to market
and commercialize new drugs in the coming years, I believe our
shareholders will continue to benefit from our unique relationship
with the Chinese government authorities, including The State
Intellectual Property Office, in terms of ensuring future patent
protection and the upholding our legal rights." Mr. Jin continued,
"These collective developments should also support Aida's
previously announced goal of growing Etimicin sales by 25% per year
on average for the next several years, while significantly reducing
the downward margin pressure previously caused by these counterfeit
products. We believe that our Etimicin growth projections are
conservative in nature and potentially subject to future upward
revisions." About Aida Pharmaceuticals: Aida Pharmaceuticals is a
product-focused pharmaceuticals company engaged in the formulation,
clinical testing, registration, manufacture, sales and marketing of
advanced pharmaceutical and genetic products in mainland China. The
Company's mission is to discover, develop and market meaningful new
therapies that improve human health. Aida Pharmaceuticals, in
operation since March 1999, is headquartered in Hangzhou, China
with manufacturing, distribution and sales points throughout
mainland China. Aida is GMP certified in China and ISO9002
certified for quality assurance and ISO14000 certified for
ecologically-friendly practices. Aida is now producing and
marketing a patented prescription drug in China: Etimicin Sulfate.
It is the first antibiotic developed in China and is regarded as a
category "A" drug by the State Food and Drug Administration of
China. Contact Information: Company: Aida Pharmaceuticals, Inc. 31
Dingjiang Road Jianggan District Hangzhou, China 310016
http://www.aidapharma.com/ Investor Relations: Equity Performance
Group Bethany Tomich (617) 723-1465
http://www.equityperformancegroup.com/ Safe Harbor Statement: Under
the Private Securities Litigation Reform Act of 1995: This press
release includes certain "forward-looking statements" within the
meaning of the United States Private Securities Litigation Reform
Act of 1995. These statements are based on Aida Pharmaceuticals,
Inc.'s management's current expectations and are subject to risks
and uncertainties and changes in circumstances. All forward-looking
statements included in this press release are based upon
information available to Aida Pharmaceuticals, Inc. as of the date
of the press release, and it assumes no obligation to update or
alter its forward looking statements whether as a result of new
information, future events or otherwise. These forward-looking
statements may relate to, among other things, plans and timing for
the introduction or enhancement of our services and products,
clinical trial results, statements about future market conditions,
supply and demand conditions, and other expectations, intentions
and plans contained in this press release that are not historical
fact. Further information on risks or other factors that could
affect Aida Pharmaceuticals, Inc.'s results of operations is
detailed in its filings with the United States Securities and
Exchange Commission available at http://www.sec.gov/. DATASOURCE:
Aida Pharmaceuticals, Inc. CONTACT: Investor Relations: Bethany
Tomich of Equity Performance Group, +1-617-723-1465, or Web site:
http://www.aidapharma.com/
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