Full Press Release Details
FOR IMMEDIATE RELEASE/February 16, 2010
| Anthony S. Marucci | Avery W. Catlin | For Media: | ||
| President and CEO | Chief Financial Officer | Matthew Driscoll | ||
| Celldex Therapeutics , Inc. | Celldex Therapeutics , Inc. | BMC Communications Group | ||
| (781) 433-0771 | (781) 433-0771 | (973) 271-6085 | ||
| IR@celldextherapeutics.com | mdriscoll@bmccommunications.com |
Million Sublicense Income Payment from TopoTarget
NEEDHAM, MA (February 16,
2010): Celldex Therapeutics, Inc. (NASDAQ: CLDX) today
announced that it has received a sublicense income payment of $3 million from
TopoTarget A/S (NASDAQ-OMX: TOPO.CO) as a result of the recent co-development
and commercialization agreement between TopoTarget and Spectrum Pharmaceuticals, Inc.
(NASDAQ: SPPI) for Belinostat, a novel histone deacetylase (HDAC) inhibitor for
the treatment of cancer. In this transaction, TopoTarget granted Spectrum a
license for the co-development and commercialization of Belinostat in North
America and India, with an option for the Chinese rights, in exchange for an
upfront cash payment of $30 million.
Based on an April 2008
agreement in which a Celldex-acquired company, CuraGen Corporation, sold the
Belinostat rights to TopoTarget, Celldex is entitled to, among other provisions,
10% of any sublicense income received by TopoTarget for Belinostat up to $6
million in the aggregate. Celldex acquired CuraGen in October 2009. Under
the April 2008 agreement, TopoTarget assumed all financial and operational
responsibility for the clinical development of Belinostat.
About Celldex Therapeutics, Inc.
Celldex Therapeutics is
the first antibody-based combination immunotherapy company. Celldex has a
pipeline of drug candidates in development for the treatment of cancer and
other difficult-to-treat diseases based on its antibody focused Precision
Targeted Immunotherapy Platform. The PTI Platform is a complementary portfolio
of monoclonal antibodies, antibody-targeted vaccines and immunomodulators used
in optimal combinations to create novel disease-specific drug candidates. For more information, please visit
Harbor Statement Under the Private Securities Litigation Reform Act of
contains forward-looking
statements made pursuant to the safe harbor provisions of the Private
Securities Litigation Reform Act of 1995, including those related to the
Company s strategic focus and the future development and commercialization of
our programs. Forward-
FOURTH AVENUE NEEDHAM, MA 02494-2725 USA 781-433-0771 FAX 781-433-0262
reflect management s current knowledge, assumptions, judgment and expectations
regarding future performance or events. Although management believes that the
expectations reflected in such statements are reasonable, they give no
assurance that such expectations will prove to be correct and you should be
aware that actual results could differ materially from those contained in the
forward-looking statements. Forward-looking statements are subject to a number
of risks and uncertainties, including, but not limited to, the uncertainties of any future
payments with respect to Belinostat, as the development and commercialization
of Belinostat is completely outside of the Celldex s control; the successful
integration of the businesses, multiple technologies and programs of CuraGen
and Celldex; our ability to adapt APC Targeting TechnologyTM to develop new, safe and effective vaccines
against oncology and infectious disease indications; our ability to
successfully complete product research and further development of our programs;
the uncertainties inherent in clinical testing; our ability to manage research
and development efforts for multiple products at varying stages of development;
Pfizer s and our strategy and business plans concerning the continued
development and commercialization of CDX-110; the timing, cost and uncertainty
of obtaining regulatory approvals; the failure of the market for the Company s
programs to continue to develop; the inability to obtain additional capital;
the inability to protect the Company s intellectual property; the loss of any
executive officers or key personnel or consultants; competition; changes in the
regulatory landscape or the imposition of regulations that affect the Company s
products; and other risks detailed from time to time in the Company s filings
with the Securities and Exchange Commission, including the Company s Form 10-K
for the fiscal year ended December 31, 2008, and its Forms