Genentech and Biogen Idec Refused a Re-hearing of U.S. Court of Appeals Decision in the Arzerra Patent Infringement Case
2013年7月16日 - 7:07AM
Company Announcement
- Genentech and Biogen Idec refused re-hearing in Arzerra
patent infringement case
COPENHAGEN, Denmark, July 15, 2013 (GLOBE NEWSWIRE) --
Genmab A/S (Copenhagen:GEN) announced today that
the U.S. Court of Appeals for the Federal Circuit has declined the
request for re-hearing. The court upheld its judgment in
favor of GlaxoSmithKline (GSK) in the patent infringement case
involving Arzerra(r) brought against GSK by Genentech and Biogen
Idec.
The lawsuit is now over unless Genentech and Biogen Idec are
granted further review by the Supreme Court.
Genentech and Biogen Idec originally filed the lawsuit in 2010
in the U.S. District Court for the Southern District of California
claiming that Arzerra infringed U.S. Patent No. 7,682,612 covering
methods of treating Chronic Lymphocytic Leukemia (CLL) with CD20
antibodies. GSK denied infringement and claimed the patent was
invalid and unenforceable. An initial judgement by the court in
favor of GSK in December 2011 was subsequently appealed by
Genentech and Biogen Idec. In April 2013 the US court of appeals
upheld the original decision by the US district court in favor of
GSK. In May 2013, Genentech and Biogen Idec filed a request for
re-hearing en banc (i.e. before all judges of the court) of the
decision from the US court of appeals stating that it was against
court precedent.
Arzerra is being developed under a co-development and
commercialization agreement between Genmab and
GlaxoSmithKline.
About Genmab A/S
Genmab is a publicly traded, international biotechnology company
specializing in the creation and development of differentiated
human antibody therapeutics for the treatment of cancer.
Founded in 1999, the company's first marketed antibody,
ofatumumab (Arzerra(r)), was approved to treat chronic lymphocytic
leukemia in patients who are refractory to fludarabine and
alemtuzumab after less than eight years in development.
Genmab's validated and next generation antibody technologies
are expected to provide a steady stream of future product
candidates. Partnering of innovative product candidates and
technologies is a key focus of Genmab's strategy and the company
has alliances with top tier pharmaceutical and biotechnology
companies. For more information visit www.genmab.com.
Contact:
Rachel Curtis Gravesen, Senior Vice President, Investor
Relations & Communications
T: +45 33 44 77 20; M: +45 25 12 62 60; E:
r.gravesen@genmab.com
This Company Announcement contains forward looking statements.
The words "believe", "expect", "anticipate", "intend" and "plan"
and similar expressions identify forward looking statements. Actual
results or performance may differ materially from any future
results or performance expressed or implied by such statements. The
important factors that could cause our actual results or
performance to differ materially include, among others, risks
associated with pre-clinical and clinical development of products,
uncertainties related to the outcome and conduct of clinical trials
including unforeseen safety issues, uncertainties related to
product manufacturing, the lack of market acceptance of our
products, our inability to manage growth, the competitive
environment in relation to our business area and markets, our
inability to attract and retain suitably qualified personnel, the
unenforceability or lack of protection of our patents and
proprietary rights, our relationships with affiliated entities,
changes and developments in technology which may render our
products obsolete, and other factors. For a further discussion of
these risks, please refer to the risk management sections in
Genmab's most recent financial reports, which are available on
www.genmab.com . Genmab does not undertake any obligation to update
or revise forward looking statements in this Company Announcement
nor to confirm such statements in relation to actual results,
unless required by law.
Genmab A/S and its subsidiaries own the following trademarks:
Genmab(r); the Y-shaped Genmab logo(r); the DuoBody(tm) logo;
HuMax(r); HuMax-CD20(r); DuoBody(r), HexaBodyTM and UniBody(r).
Arzerra(r) is a trademark of GlaxoSmithKline.
Company Announcement no. 31 CVR no. 2102 3884
Genmab A/S Bredgade 34E 1260 Copenhagen K Denmark