Published: June 04, 2010
Markman Hearing Cancelled in Cubist Pharmaceuticals' Patent Infringement Action Against Teva Parenteral Medicines, Inc.
LEXINGTON, Mass. - (BUSINESS WIRE) - Cubist Pharmaceuticals, Inc. (NASDAQ: CBST) today announced that the
U.S. District Court for the District of Delaware notified Cubist that
the Markman hearing previously scheduled for June 9, 2010 has
been cancelled. The court stated that a claim construction order will
issue in due course.
Cubist filed a patent infringement lawsuit against Teva Parenteral
Medicines, Inc. (TPM), Teva Pharmaceuticals USA, Inc. and Teva
Pharmaceutical Industries Ltd. The complaint alleges infringement of US
Patent Nos. 6,468,967 and 6,852,689, which expire on September 24, 2019,
and US Patent No. RE39,071, which expires on June 15, 2016.
About CUBICIN
CUBICIN (daptomycin for injection) is approved in the U.S. and many
other markets as therapy for Staphylococcus aureus bloodstream
infections (bacteremia), including right-sided endocarditis caused by
methicillin-resistant S. aureus (MRSA), and complicated skin
infections caused by certain Gram-positive bacteria, including MRSA.
CUBICIN is not indicated for the treatment of pneumonia. Most adverse
events reported in clinical trials were mild to moderate in intensity.
The most common were anemia, constipation, diarrhea, nausea, vomiting,
injection site reactions, and headache. To reduce the development of
drug-resistant bacteria and maintain the effectiveness of CUBICIN,
CUBICIN should be used only to treat or prevent infections that are
proven or strongly suspected to be caused by bacteria susceptible to
CUBICIN. For full prescribing information, visit www.cubicin.com.
About Cubist
Cubist Pharmaceuticals, Inc. is a biopharmaceutical company focused on
the research, development, and commercialization of pharmaceutical
products that address unmet medical needs in the acute care environment.
In the U.S., Cubist markets CUBICIN (daptomycin for injection), the
first antibiotic in a new class of anti-infectives called lipopeptides.
Cubist also promotes MERREM I.V. (meropenem for injection) in the U.S.
under an agreement with AstraZeneca. The Cubist clinical product
pipeline currently consists of a Phase 2 program, added with Cubist's
acquisition of Calixa Therapeutics Inc. in December 2009, focused on the
development of a novel cephalosporin to address certain serious
infections caused by multi-drug resistant (MDR) Gram-negative organisms;
a Phase 2 program for the treatment of CDAD (Clostridium difficile-associated
diarrhea); and a Phase 1 program intended to address the unmet medical
need for a treatment for serious infections caused by MDR Gram-negative
pathogens. Cubist is also working on several pre-clinical programs being
developed to address areas of significant medical needs. These include
an anti-infective program for the treatment of respiratory syncytial
virus (RSV) in children, therapies to treat various serious bacterial
infections, and agents to treat acute pain. Cubist is headquartered in
Lexington, Mass. Additional information can be found at Cubist's web
site at www.cubist.com.
Cubist and CUBICIN are registered trademarks of Cubist Pharmaceuticals,
Inc.
AstraZeneca and MERREM are trademarks of the AstraZeneca group
of companies.
Cubist and CUBICIN are registered trademarks of Cubist Pharmaceuticals,
Inc.
AstraZeneca and MERREM are registered trademarks of the
AstraZeneca group of companies.

Cubist Pharmaceuticals, Inc.
Eileen C. McIntyre, 781-860-8533
Senior
Director, Corporate Communications
eileen.mcintyre@cubist.com
or
Weber
Shandwick
Tara Murphy, 617-520-7045
tara.murphy@webershandwick.com
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