GAITHERSBURG, Md., Dec. 8 /PRNewswire-FirstCall/ -- MedImmune, Inc.
(Nasdaq: MEDI) announced today that it continues to build upon its corporate
initiatives to expand and expedite the development of its product pipeline by
licensing rights to antibody-enhancing technologies. The latest technology
agreements MedImmune has entered into are with BioWa, Inc. and Xencor, Inc.
from which MedImmune has gained access to two different technologies that may
enhance the effectiveness of monoclonal antibodies (MAbs) targeting cancer.
'As a leader in the biotechnology industry dedicated to advancing science
for better health, MedImmune aims to maintain its competitive edge by
investing in technologies that will help develop successful biopharmaceutical
therapies,' commented Peter Kiener, D.Phil., MedImmune senior vice president,
research.
'In the future, we plan to continue to be aggressive on the in-licensing
and collaboration front in support of our strategic priority of elevating
science and evolving our research and development governance,' said Edward T.
Mathers, senior vice president, corporate development.
MedImmune's recent technology licensing agreements include:
Avidia, Inc. -- MedImmune intends to combine its growing expertise in the
field of tyrosine kinase research with Avidia's Avimer technology to develop
anti-cancer product candidates that may have several advantages over
antibodies in terms of biological activity, tissue distribution, reduced
immunogenicity and improved manufacturing efficiencies. The two companies are
also collaborating on the development of anti-cancer products targeting cMET,
a receptor tyrosine kinase found in high levels in certain cancer cells.
Avalon Pharmaceuticals, Inc. -- MedImmune and Avalon are using Avalon's
proprietary drug discovery technology, the AvalonRx(R) drug discovery engine,
to collaborate on discovery and optimization of small molecule therapeutic
compounds for the prevention and treatment of debilitating disease.
BioWa, Inc. -- MedImmune licensed the right to use BioWa's POTELLIGENT
technology as a method for maximizing the potential of therapeutic antibodies
targeting cancer.
Seattle Genetics, Inc. (Nasdaq: SGEN) -- MedImmune in-licensed Seattle
Genetics' antibody-drug conjugate, which utilizes the targeting ability of
MAbs to deliver cell-killing payloads to specific cells.
Xencor, Inc. -- MedImmune licensed the right to use Xencor's XmAb(TM)
proprietary engineered Fc domains in development of MAbs against select cancer
targets.
About MedImmune, Inc.
MedImmune strives to provide better medicines to patients, new medical
options for physicians, rewarding careers to employees, and increased value to
shareholders. Dedicated to advancing science and medicine to help people live
better lives, the company is focused on the areas of infectious diseases,
cancer and inflammatory diseases. With more than 2,000 employees worldwide,
MedImmune is headquartered in Maryland. For more information, visit the
company's website at http://www.medimmune.com .
This announcement contains, in addition to historical information, certain
'forward-looking statements' regarding MedImmune's monoclonal antibody
development programs. Such forward-looking statements are based on current
expectations and involve inherent risks and uncertainties, including factors
that could delay, divert or change current expectations and could cause actual
outcomes and results to differ materially from current expectations. In
addition to risks and uncertainties discussed in MedImmune's filings with the
U.S. Securities and Exchange Commission, no assurance exists that development
efforts will succeed, that the antibodies will receive required regulatory
approval or that, even if regulatory approval is received, the antibody
products will be commercially successful. MedImmune undertakes no obligation
to update any forward-looking statement, whether as a result of new
information, future events or otherwise except as may be required by
applicable law or regulation.
SOURCE MedImmune, Inc.