Memorandum to Shareholders From Dr. Amnon Gonenne, MabCure’s Chief Executive Officer
01 Junio 2010 - 7:00AM
Business Wire
MabCure, Inc. (OTCBB:MBCI):
Dear Shareholders:
I am pleased to update you on the progress of our research and
development.
Over the past several months we have been working intensively on
advancing our various programs with an emphasis on melanoma and
ovarian cancer diagnostics. We consider these two projects
near-term in their respective development stages, as I describe
below.
In January 2010, we announced the commencement of our clinical
trials at the Ramathibodi Hospital in Bangkok, Thailand to evaluate
the potential of our panel of monoclonal antibodies (MAbs) to
diagnose ovarian cancer in high risk patients. Since the study
began, patients have been recruited at a solid pace and in line
with our schedule. In addition, we are privileged that the Thai
National Cancer Institute has decided to join our study and is
currently reviewing our study protocol. The study is estimated to
be completed within 5-6 months, as originally planned.
In parallel to our study in Thailand, we are planning to
commence a study in collaboration with a major medical center in
Belgium of several hundred blood samples which were obtained from
patients over the past several years. The purpose of this
“retrospective” study is to provide additional proof of the ability
of our MAbs to correctly diagnose ovarian cancer, and is of
considerable importance given the significant number of blood
samples to be tested.
The study will be “blind” to all involved (i.e. the samples will
be coded and neither the clinicians nor MabCure scientists will
know the identity of the specimens until the study is complete), so
as to prevent any bias in the analysis of the results. The study is
expected to last several weeks and will commence once a formal
agreement has been signed with the Belgian medical center. As a
prelude to this study, we conducted a pilot study on a limited
number of these “retrospective” specimens to calibrate the optimal
technical conditions for our MAbs.
In parallel, we are conducting an independent study in Germany
aimed at testing the ability of our antibodies to bind to different
ovarian cancer tissue specimens. The purpose of the study is to
select those antibodies which are most suitable for use as imaging
agents and therapeutic agents. Results from this study are expected
within 2 months.
We have also made progress with our anti-melanoma MAbs. Melanoma
is the most lethal form of skin cancer, accounting for 75% of
deaths from skin cancers. The survival rate for advanced melanoma
is as low as 15 percent, but if detected early (before the tumor
penetrates the epidermis) the survival rate can reach 99%.
According to the National Cancer Institute (NCI), 1 in every 53
people in the U.S. will be diagnosed with melanoma of the skin
during their lifetime.
In addition, between to 2 to 8 percent of the Caucasian
population in the U.S. and Europe are at a significant increased
risk for developing melanoma from the appearance of atypical moles
(known as dysplastic nevi or DN) on their skins. This translates to
approximately 4M-16M people in the U.S. and 10M-40M people in
Europe. Consequently, there is a significant unmet need to identify
those moles which have been transformed into melanoma.
We recently initiated an independent third-party study in the
U.K. of our antibodies for diagnosing melanoma in tissue specimens.
The purpose of the study is to obtain rigorous proof of the
specificity of our MAbs, using standards required by the U.S.
FDA.
We plan to initiate a follow-up clinical study of our
anti-melanoma MAbs by a highly esteemed European group which
specializes in melanoma. The purpose of this study is to prepare
the groundwork for entering the European market with a diagnostic
MAb for Melanoma. Negotiations for this study are currently
underway and we will issue a separate press release once the study
commences.
It is important to note that the results of the various melanoma
studies described above will enhance our patent application
position as well as will advance the application of these MAbs as
imaging agents and diagnostic agents for melanoma.
In our R&D pipeline, we have a planned pilot clinical study
at the Ramathibodi Hospital in Bangkok, Thailand for the diagnosis
of prostate cancer in the urine and blood of high risk patients.
The study protocol will be submitted shortly to the hospital’s
Ethics Committee for approval. The study is scheduled to begin in
August and is expected to be completed by the end of the year.
I would like to reassure our shareholders that we are working
assiduously to reach our milestones and to obtain clinical
breakthroughs, which will benefit cancer patients as well as our
investors. I would like to take this opportunity to thank all of
our shareholders for their continued support and belief in our
company.
Yours sincerely, Dr. Amnon Gonenne President & CEO MabCure,
Inc.
About MabCure, Inc.
MabCure is a biotechnology company whose vision is to change the
perception of cancer as being a largely incurable disease. MabCure
owns proprietary technology for the creation of unique and highly
specific monoclonal antibodies (MAbs), which we plan to develop as
diagnostic tools, imaging agents, and drugs to treat lethal
cancers. MabCure’s initial goal is to develop its novel MAbs as
diagnostic tools for the detection of Ovarian and Melanoma cancers
at an early stage, when these diseases are still localized and
highly curable. For further information visit the Company’s website
at www.mabcure.com.
This news release contains “forward-looking statements”.
Statements in this news release which are not purely historical are
forward-looking statements and include any statements regarding
beliefs, plans, expectations or intentions regarding the future.
Actual results could differ from those projected in any
forward-looking statements due to numerous factors. Such factors
include, among others, the change of business focus of the
management of the Company and the inability of the Company to
pursue its current objectives. These forward-looking statements are
made as of the date of this news release and the Company assumes no
obligation to update the forward-looking statements, or to update
the reasons why actual results could differ from those projected in
the forward-looking statements.
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