HAMPTON, N.J., Aug. 11, 2016 (GLOBE NEWSWIRE) -- Celldex Therapeutics, Inc. (NASDAQ:CLDX) today announced that
the Company has promoted Elizabeth Crowley to the newly created position of Senior Vice President, Chief Product Development
Officer. Ms. Crowley was previously Senior Vice President of Product Development of Celldex and brings almost 25 years of industry
experience where she was responsible for leading the execution of multiple successful drug development programs.
“Celldex was founded on the belief that combination regimens designed to unlock the power of the immune system would deliver the
greatest benefit to the largest population of patients,” said Anthony Marucci, Co-founder, President and Chief Executive Officer of
Celldex Therapeutics. “This newly created position is a direct response to the future of portfolio planning and drug development in
the immuno-oncology field where we believe multi-drug combination regimens will become the norm and the development programs to
explore these opportunities will become increasingly complex. Beth’s deep, oncology-focused experience in strategic planning,
portfolio management and implementation have played a critical role in building the depth and breadth of our pipeline to date and
an exceptional development operations team here at Celldex. We look forward to her continued expertise in this expanded leadership
role.”
"Celldex has thoughtfully seeded a pipeline with individual product candidates that uniquely manipulate the immune system at key
points,” said Ms. Crowley. “With successful proof of concept work achieved, we have now entered the next phase of development and
are extensively exploring multi-drug combination regimens. I look forward to working closely with my Celldex colleagues across the
organization as we expand this approach in our ongoing efforts to improve outcomes for patients and their families.”
Ms. Crowley joined Celldex in 2009 as Vice President, Clinical Development. Prior to that, she held several senior level roles
at CuraGen Corporation, most recently serving as the Vice President of Development Operations, responsible for strategic and
operational development activities of the oncology and oncology supportive care portfolio, regulatory affairs, clinical operations
and data management. Ms. Crowley started her career at Bayer Corporation in 1992, holding various positions providing leadership of
clinical research and project management prior to completing her tenure there as the Director of Global Study Audit Management,
assuring the highest standards for program execution. Ms. Crowley received her BS in Chemistry with a concentration in Business
from Boston College.
About Celldex Therapeutics, Inc.
Celldex is developing targeted therapeutics to address devastating diseases for which available treatments are inadequate. Our
pipeline is built from a proprietary portfolio of antibodies and immunomodulators used alone and in strategic combinations to
create novel, disease-specific therapies that induce, enhance or suppress the body's immune response. Visit www.celldex.com.
Forward Looking Statement
This release 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 (by Celldex and others) of glembatumumab vedotin ("glemba"; CDX-011), varlilumab (“varli”; CDX-1127) and other
products and our goals for 2016. Forward-looking statements 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 or that those goals will be
achieved, 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, our
ability to successfully complete research and further development and commercialization of glembatumumab vedotin and other drug
candidates; our ability to obtain additional capital to meet our long-term liquidity needs on acceptable terms, or at all,
including the additional capital which will be necessary to complete the clinical trials that we have initiated or plan to
initiate; the uncertainties inherent in clinical testing and accruing patients for clinical trials; our limited experience in
bringing programs through Phase 3 clinical trials; our ability to manage and successfully complete multiple clinical trials and the
research and development efforts for our multiple products at varying stages of development; the availability, cost, delivery and
quality of clinical and commercial grade materials produced by our own manufacturing facility or supplied by contract
manufacturers, who may be our sole source of supply; the timing, cost and uncertainty of obtaining regulatory approvals; our
ability to maintain and derive benefit from the Fast Track designation for glembatumumab vedotin which does not change the
standards for regulatory approval or guarantee regulatory approval on an expedited basis, or at all; the failure of the market for
the Company's programs to continue to develop; our ability 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 factors listed under "Risk Factors" in our annual report on Form 10-K and
quarterly reports on Form 10-Q.
All forward-looking statements are expressly qualified in their entirety by this cautionary notice. You are cautioned not to
place undue reliance on any forward-looking statements, which speak only as of the date of this release. We have no obligation, and
expressly disclaim any obligation, to update, revise or correct any of the forward-looking statements, whether as a result of new
information, future events or otherwise.
Company Contact Sarah Cavanaugh Vice President of Investor Relations & Corp Communications Celldex Therapeutics, Inc. (781) 433-3161 scavanaugh@celldex.com Charles Liles Associate Director of Investor Relations & Corp Communications Celldex Therapeutics, Inc. (781) 433-3107 cliles@celldex.com Media Inquiries Dan Budwick Pure Communications, Inc. (973) 271-6085 dan@purecommunicationsinc.com