Bioenvision Names Vice President of Regulatory Affairs
October 24 2006 - 7:00AM
Business Wire
Bioenvision, Inc. (NasdaqGM:BIVN) today announced MaryJane Rafii,
Ph.D. has joined the Company as Vice President, Regulatory Affairs
effective October 30th. Dr. Rafii brings to Bioenvision over 12
years of pharmaceutical and biotechnology industry experience. The
appointment signals the Company�s focus on expanding the markets
for its approved products and developing the product pipeline. Dr.
Rafii was most recently the head of regulatory affairs at the
Ludwig Institute for Cancer Research in Manhattan where she had
been since 1999. Dr. Rafii also oversaw regulatory affairs at
Sankyo USA in New York from 1995 to 1999. She began her regulatory
career at Escalon Ophthalmics in 1993. �Dr. Rafii has the
background to design regulatory strategies appropriate for each of
the products in our pipeline and to manage certain of our clinical
programs we have designed or hope to design for our approved
products. We are delighted to have added MaryJane to our team,�
said David P. Luci, Chief Financial Officer and General Counsel of
Bioenvision. �Dr. Rafii�s background in oncology will be
instrumental in expanding the franchise for our leukemia drug
Evoltra� (clofarabine),� said Dr. Christopher B. Wood, Chairman and
Chief Executive Officer of Bioenvision. �This drug has shown an
indication of activity for treating several types of cancer and on
a global basis could reach blockbuster status. Dr. Rafii will help
the Company maximize the potential for this innovative new
therapy.� MaryJane Rafii earned her Ph.D. in immunology and
biochemistry from the University of Cardiff, Wales, United Kingdom.
She received her master�s degree in protein modeling from UC San
Francisco and a bachelor�s degree in molecular biology/marketing
and international finance from the University of Southern
California. About Bioenvision Bioenvision's primary focus is the
acquisition, development, distribution and marketing of compounds
and technologies for the treatment of cancer. Bioenvision has a
broad pipeline of products for the treatment of cancer, including:
Evoltra�, Modrenal� (for which Bioenvision has obtained regulatory
approval for marketing in the United Kingdom for the treatment of
post-menopausal breast cancer following relapse to initial hormone
therapy), and other products. Bioenvision is also developing
anti-infective technologies, including the OLIGON� technology, an
advanced biomaterial that has been incorporated into various FDA
approved medical devices and Suvus�, an antimicrobial agent
currently in clinical development for refractory chronic hepatitis
C infection. For more information on Bioenvision please visit our
Web site at www.bioenvision.com. Certain statements contained
herein are "forward-looking" statements (as such term is defined in
the Private Securities Litigation Reform Act of 1995). Because
these statements include risks and uncertainties, actual results
may differ materially from those expressed or implied by such
forward-looking statements. Specifically, factors that could cause
actual results to differ materially from those expressed or implied
by such forward-looking statements include, but are not limited to:
risks associated with preclinical and clinical developments in the
biopharmaceutical industry in general and in Bioenvision's
compounds under development in particular; the potential failure of
Bioenvision's compounds under development to prove safe and
effective for treatment of disease; uncertainties inherent in the
early stage of Bioenvision's compounds under development; failure
to successfully implement or complete clinical trials; failure to
receive marketing clearance from regulatory agencies for our
compounds under development; acquisitions, divestitures, mergers,
licenses or strategic initiatives that change Bioenvision's
business, structure or projections; the development of competing
products; uncertainties related to Bioenvision's dependence on
third parties and partners; and those risks described in
Bioenvision's filings with the SEC. Bioenvision disclaims any
obligation to update these forward-looking statements. Bioenvision,
Inc. (NasdaqGM:BIVN) today announced MaryJane Rafii, Ph.D. has
joined the Company as Vice President, Regulatory Affairs effective
October 30th. Dr. Rafii brings to Bioenvision over 12 years of
pharmaceutical and biotechnology industry experience. The
appointment signals the Company's focus on expanding the markets
for its approved products and developing the product pipeline. Dr.
Rafii was most recently the head of regulatory affairs at the
Ludwig Institute for Cancer Research in Manhattan where she had
been since 1999. Dr. Rafii also oversaw regulatory affairs at
Sankyo USA in New York from 1995 to 1999. She began her regulatory
career at Escalon Ophthalmics in 1993. "Dr. Rafii has the
background to design regulatory strategies appropriate for each of
the products in our pipeline and to manage certain of our clinical
programs we have designed or hope to design for our approved
products. We are delighted to have added MaryJane to our team,"
said David P. Luci, Chief Financial Officer and General Counsel of
Bioenvision. "Dr. Rafii's background in oncology will be
instrumental in expanding the franchise for our leukemia drug
Evoltra(R) (clofarabine)," said Dr. Christopher B. Wood, Chairman
and Chief Executive Officer of Bioenvision. "This drug has shown an
indication of activity for treating several types of cancer and on
a global basis could reach blockbuster status. Dr. Rafii will help
the Company maximize the potential for this innovative new
therapy." MaryJane Rafii earned her Ph.D. in immunology and
biochemistry from the University of Cardiff, Wales, United Kingdom.
She received her master's degree in protein modeling from UC San
Francisco and a bachelor's degree in molecular biology/marketing
and international finance from the University of Southern
California. About Bioenvision Bioenvision's primary focus is the
acquisition, development, distribution and marketing of compounds
and technologies for the treatment of cancer. Bioenvision has a
broad pipeline of products for the treatment of cancer, including:
Evoltra(R), Modrenal(R) (for which Bioenvision has obtained
regulatory approval for marketing in the United Kingdom for the
treatment of post-menopausal breast cancer following relapse to
initial hormone therapy), and other products. Bioenvision is also
developing anti-infective technologies, including the OLIGON(R)
technology, an advanced biomaterial that has been incorporated into
various FDA approved medical devices and Suvus(R), an antimicrobial
agent currently in clinical development for refractory chronic
hepatitis C infection. For more information on Bioenvision please
visit our Web site at www.bioenvision.com. Certain statements
contained herein are "forward-looking" statements (as such term is
defined in the Private Securities Litigation Reform Act of 1995).
Because these statements include risks and uncertainties, actual
results may differ materially from those expressed or implied by
such forward-looking statements. Specifically, factors that could
cause actual results to differ materially from those expressed or
implied by such forward-looking statements include, but are not
limited to: risks associated with preclinical and clinical
developments in the biopharmaceutical industry in general and in
Bioenvision's compounds under development in particular; the
potential failure of Bioenvision's compounds under development to
prove safe and effective for treatment of disease; uncertainties
inherent in the early stage of Bioenvision's compounds under
development; failure to successfully implement or complete clinical
trials; failure to receive marketing clearance from regulatory
agencies for our compounds under development; acquisitions,
divestitures, mergers, licenses or strategic initiatives that
change Bioenvision's business, structure or projections; the
development of competing products; uncertainties related to
Bioenvision's dependence on third parties and partners; and those
risks described in Bioenvision's filings with the SEC. Bioenvision
disclaims any obligation to update these forward-looking
statements.
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