Cougar Biotechnology Announces Initiation of Phase I/II Trial of CB7630 (Abiraterone Acetate) in Advanced Breast Cancer Patients
20 November 2008 - 2:05PM
Business Wire
Cougar Biotechnology, Inc. (NASDAQ: CGRB) today announced that the
first patient was enrolled in a Phase I/II clinical trial of the
Company�s drug candidate CB7630 (abiraterone acetate), an orally
active inhibitor of the steroidal enzyme 17alpha-hydroxylase/C17,20
lyase, for the treatment of advanced breast cancer. The Phase I/II
trial is being conducted at The Institute of Cancer Research in
London and managed by the Drug Development Office of Cancer
Research UK, which is funding the trial. The Phase I/II clinical
trial, which is open only to UK women, is an open label, dose
escalating study to evaluate the safety and efficacy of CB7630
administered daily to patients with estrogen receptor (ER) positive
or androgen receptor (AR) positive, metastatic breast cancer.
Patients enrolled in the trial have disease that has progressed
after at least two lines of hormonal therapies, such as aromatase
inhibitors and tamoxifen. Dr. Johann S. de Bono, MSc, PhD, MD,
FRCP, the principal investigator of the trial from The Institute of
Cancer Research, said, "We are pleased to begin enrolling patients
in this Phase I/II trial. The mechanism of action of CB7630 may
result in the inhibition of many androgenic steroids that may be
contributing to disease progression in breast cancer patients. We
greatly look forward to continuing enrollment of patients in this
Phase I/II trial and further investigating the safety and efficacy
of this novel, targeted therapy in breast cancer patients." Dr.
Sally Burtles, Cancer Research UK�s director of drug development,
added, �For women with advanced breast cancer who have stopped
responding to the standard treatment available, abiraterone may
provide another treatment option.� Alan H. Auerbach, Chief
Executive Officer and President of Cougar Biotechnology, said,
"Initiating the Phase I/II clinical trial of CB7630 in breast
cancer patients is an important milestone for the Company and for
the clinical development of the drug, as it represents a second
potential indication for CB7630." Arturo Molina, M.D., M.S., FACP,
Cougar's Chief Medical Officer and Executive Vice President of
Clinical Research and Development, added, "Our clinical trials of
CB7630 in advanced prostate cancer patients to date have
demonstrated that treatment with CB7630 results in a strong
reduction in many of the androgens in the endocrinological pathway,
and we believe these androgens may also be driving breast cancer
progression. We look forward to future advancement of the clinical
development of CB7630 in breast cancer." About Cougar
Biotechnology, Inc. Cougar Biotechnology, Inc. is a Los
Angeles-based biotechnology company established to in-license and
develop clinical stage drugs, with a specific focus on the field of
oncology. Cougar�s oncology portfolio includes CB7630, a targeted
inhibitor of the 17-alpha hydroxylase/C17,20 lyase enzyme, which is
currently being studied in a Phase III clinical trial in prostate
cancer and a Phase I/II trial in breast cancer; CB3304, an
inhibitor of microtubule dynamics, which is currently in a Phase I
trial in multiple myeloma; and CB1089, an analog of vitamin D,
which has been clinically tested in a number of solid tumor types.
Further information about Cougar can be found at
www.cougarbiotechnology.com. About The Institute of Cancer Research
The Institute of Cancer Research is Europe�s leading cancer
research centre with expert scientists working on cutting edge
research. It was founded in 1909 to carry out research into the
causes of cancer and to develop new strategies for cancer
prevention, diagnosis, treatment and care.�For more information,
visit www.icr.ac.uk. About Cancer Research UK Cancer Research UK, a
leading charity dedicated to cancer research, develops novel
treatments for cancer. It currently has a portfolio of
approximately 40 new anti-cancer agents in preclinical, Phase I or
early Phase II clinical development. Since 1982, the Drug
Development Office of Cancer Research UK has taken over 100
potential new anti-cancer agents into clinical trials in patients.
For more information on UK cancer trials, visit
www.cancerhelp.org.uk. This press release contains forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995. These statements are often, but not always,
made through the use of words or phrases such as "anticipates,"
"expects," "plans," "believes," "intends," and similar words or
phrases. These forward-looking statements include, without
limitation, statements related to theories about the mechanism of
action of CB7630 and benefits that may be derived from Cougar�s
drug development programs, including the potential advantages of
CB7630 and its potential for use in the treatment of advanced
breast cancer and prostate cancer. Such statements involve risks
and uncertainties that could cause Cougar�s actual results to
differ materially from the anticipated results and expectations
expressed in these forward-looking statements. These statements are
only predictions based on current information and expectations and
involve a number of risks and uncertainties. Actual events or
results may differ materially from those projected in any of such
statements due to various factors, including the risks and
uncertainties inherent in clinical trials, and drug development and
commercialization. For a discussion of these and other factors,
please refer to Cougar�s annual report on Form 10-KSB for the year
ended December 31, 2007, as well as other subsequent filings with
the Securities and Exchange Commission. You are cautioned not to
place undue reliance on these forward-looking statements, which
speak only as of the date hereof. This caution is made under the
safe harbor provisions of the Private Securities Litigation Reform
Act of 1995. All forward-looking statements are qualified in their
entirety by this cautionary statement and Cougar undertakes no
obligation to revise or update this press release to reflect events
or circumstances after the date hereof.
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