Bioenvision Appoints Michael Kauffman, M.D., Ph.D, to Board Of Directors.Business Editors/Health/Medical Writers NEW YORK--(BUSINESS WIRE)--Jan. 26, 2004 Bioenvision, Inc. (Amex:BIV BIV Bivouac BiV Biventricular BIV Bovine Immunodeficiency Virus BIV Built-in Variable (plumbing) ) today announced that Michael Kauffman, M.D., Ph.D., has been elected to its board of directors. Dr. Kauffman currently serves as President and CEO (1) (Chief Executive Officer) The highest individual in command of an organization. Typically the president of the company, the CEO reports to the Chairman of the Board. of Predix Pharmaceuticals Inc., a privately owned drug discovery and development company. Dr. Kauffman received his M.D. and Ph.D. (Biochemistry, Cell and Molecular Biology Cell and Molecular Biology may refer to:
Harvard College, originally for men, was founded in 1636 with a grant from the General Court of the Massachusetts Bay Colony. . He is board certified board certified, adj the status of a dental specialist such as an orthodontist who has become a board diplomate by successfully completing the certification program of the recognized certification board in that area of practice. in internal medicine and has over 10 years of extensive experience in drug discovery and development. "We are pleased to bring Michael Kauffman's drug development expertise to the board of directors of Bioenvision," commented Dr. Christopher B. Wood, Chairman and CEO of Bioenvision. "While Vice President of Medicine at Millennium Pharmaceuticals Inc., Michael played a key role in fostering the expedited approval of VELCADE(TM), one of the most novel oncology compounds approved by the FDA FDA abbr. Food and Drug Administration FDA, n.pr See Food and Drug Administration. FDA, n.pr the abbreviation for the Food and Drug Administration. . The speed of the approval speaks to Michael's expertise in designing and executing clinical development strategies. We look forward to his guidance as we bring our lead drugs to market." Prior to joining Predix, Dr. Kauffman held positions of increasing responsibility at Millennium Pharmaceuticals Inc. where he most recently served as Vice President of Medicine and Leader of the VELCADE Development Program. Prior to that, Dr. Kauffman held senior positions at Millennium Predictive Medicine, Inc., which was acquired by Millennium Pharmaceuticals in 2000. Dr. Kauffman has also worked with Biogen Corporation where he served as medical director of the inflammation program and in other managerial positions. Dr. Kauffman is the author of numerous medical publications and is the publisher and President of OutlineMed Inc., a developer of medical information software. About Bioenvision Bioenvision's (Amex:BIV) primary focus is the development and distribution of compounds and technologies for the treatment of cancer. Bioenvision has a broad pipeline of products for the treatment of cancer, including: clofarabine (in co-development with ILEX Ilex a bush bearing berries containing saponins; cause vomiting, diarrhea. Called also holly. Oncology, Inc.), 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 Hormone therapy Treating cancers by changing the hormone balance of the body, instead of by using cell-killing drugs. Mentioned in: Breast Cancer, Thyroid Cancer hormone therapy ), and other products in clinical trials. Bioenvision is also developing anti-infective technologies, including the OLIGON technology; an advanced biomaterial biomaterial /bio·ma·te·ri·al/ (bi?o-mah-ter´e-al) a synthetic dressing with selective barrier properties, used in the treatment of burns; it consists of a liquid solvent (polyethylene glycol-400) and a powdered polymer. that has been incorporated into various FDA approved medical devices. 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 The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and 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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