ChemGenex Appoints Mr. Thomas DeZao as Senior Vice President and Chief Commercial Officer
July 20 2009 - 7:00AM
Business Wire
ChemGenex Pharmaceuticals Limited (ASX:CXS) announced today that
it has appointed Mr. Thomas DeZao to the position of Senior Vice
President and Chief Commercial Officer. Mr. DeZao will commence his
position immediately and will lead the company�s commercial efforts
including sales, marketing and the coordination of manufacturing
activities for the launch of omacetaxine in the USA.
"Tom is a highly respected executive in the pharmaceuticals
industry and we are delighted that he will be joining ChemGenex as
he brings the crucial experience and expertise to lead a successful
launch of omacetaxine in the U.S. next year,� said Dr. Greg
Collier, Chief Executive Officer and Managing Director. �This is an
exciting stage in the company�s development; we are on track to
complete the submission of our NDA to the U.S. FDA in Q3, 2009 with
the European submission to the EMEA due Q4, 2009.�
Mr. DeZao has more than 25 years of drug sales and marketing
experience and a significant track record of achievement with
several pharmaceutical companies who have launched innovative
products in the U.S. oncology market. Most recently, Mr. DeZao
spent six years at Genitope Corporation as Vice President of
Strategic Marketing and Sales, where he created a solid foundation
for the commercialization of the MyVax� Personalized Immunotherapy
for the treatment of follicular non-Hodgkin's lymphoma (f-NHL).
Prior to joining Genitope, Mr. DeZao was the Vice President of
Marketing and Medical Affairs at Corixa/Coulter Pharmaceuticals
Inc, where he played a pivotal role in the highly successful
collaboration with GlaxoSmithKline to develop and launch BEXXAR�.
Previously Mr. DeZao held commercial positions of increasing
responsibility with Asta Medica Inc. and Chiron Corporation.
�I am thrilled to join the ChemGenex team at this pivotal period
in the company�s development and look forward to this unique
opportunity to plan and implement the launch of a new and important
oncology product that has the potential to positively impact the
lives of leukemia patients,� added Thomas DeZao.
Omacetaxine Overview
Omacetaxine mepesuccinate is a first-in-class cetaxine with
demonstrated clinical activity as a single agent in a range of
hematological malignancies. Omacetaxine has a novel mechanism of
action, specifically binding to the ribosomal A-site cleft and
inhibiting protein translation of short-lived oncoproteins that are
upregulated in leukemic cells (particularly Cyclin-D1, Mcl-1 and
c-Myc). As omacetaxine acts independently of tyrosine kinase
inhibitors, it may have a therapeutic advantage for patients who
have developed resistance to TKIs. Omacetaxine is administered
subcutaneously. Omacetaxine is currently in global phase 2/3
clinical trials for chronic myeloid leukemia (CML) and has been
granted Orphan Drug designations by the U.S. Food and Drug
Administration (FDA) and European Medicines Agency (EMEA) as well
as Fast Track status by the FDA.
About ChemGenex Pharmaceuticals Limited
(http://www.chemgenex.com)
ChemGenex Pharmaceuticals is a pharmaceutical development
company dedicated to improving the lives of patients by developing
personalized oncology medicines. ChemGenex harnesses the power of
genomics both to discover novel targets and drug compounds, and in
clinical trials to develop more individualized treatment outcomes.
ChemGenex�s lead compound, omacetaxine mepesuccinate, is currently
in phase 2/3 clinical trials for chronic myeloid leukemia (CML).
ChemGenex has a second anticancer compound, amonafide
dihydrochloride (Quinamed�), which is in phase 2 clinical
development for various solid cancers, and a portfolio of assets in
pre-clinical development. ChemGenex currently trades on the
Australian Stock Exchange under the symbol "CXS" and as a level 1
ADR program on the US OTC market under the symbol "CXSPY". For
additional information on ChemGenex Pharmaceuticals, please visit
our web site at http://www.chemgenex.com.
Details on the clinical trials can be accessed from the
following websites;
http://clinicaltrials.gov/ct2/show/NCT00375219?term=homoharringtonine&rank=9
and http://www.tkiresistantcmltrials.com
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to which a hyperlink has been provided) that use the words
�estimate�, �project�, �intend�, �expect�, �believe� and similar
expressions are intended to identify forward-looking statements
within the meaning of the US Private Securities Litigation Reform
Act of 1995. These forward-looking statements involve known and
unknown risks and uncertainties which could cause the actual
results, performance or achievements of the company to be
materially different from those which may be expressed or implied
by such statements, including, among others, risks or uncertainties
associated with the development of the company�s technology, the
ability to successfully market products in the clinical pipeline,
the ability to advance promising therapeutics through clinical
trials, the ability to establish our fully integrated technologies,
the ability to enter into additional collaborations and strategic
alliances and expand current collaborations and obtain milestone
payments, the suitability of internally discovered genes for drug
development, the ability of the company to meet its financial
requirements, the ability of the company to protect its proprietary
technology, potential limitations on the company�s technology, the
market for the company�s products, government regulation in
Australia and the United States, changes in tax and other laws,
changes in competition and the loss of key personnel. These
statements are based on our management�s current expectations and
are subject to a number of uncertainties that could change the
results described in the forward-looking statements. Investors
should be aware that there are no assurances that results will not
differ from those projected.
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