Dendreon Corporation Appoints Israel Rios, M.D., Vice President of Clinical Affairs.Business Editors & Health/Medical Writers BIOWIRE2K SEATTLE--(BUSINESS WIRE)--Jan. 8, 2003 Dendreon Corporation (Nasdaq:DNDN) today announced that Israel Rios, M.D., has joined the company as vice president of clinical affairs. Rios joins Dendreon from Berlex Laboratories Introduction Berlex Laboratories, Incorporated is a research-based pharmaceutical company headquartered in Montville, New Jersey with operations in Wayne, New Jersey; Bothell, Washington; Seattle, Washington; and Richmond, California. , Inc., the U.S. affiliate of Schering AG, Germany (NYSE NYSE See: New York Stock Exchange :SHR SHR Shore SHR Spontaneously Hypertensive Rat SHR Staff Human Resources SHR Saskatoon Health Region (Saskatoon, SK, Canada) SHR Shift Logical Right SHR Sensible Heat Ratio SHR Supplementary Homicide Report SHR Steroid Hormone Receptor ), where he most recently served as vice president of oncology development. Rios brings more than 25 years of industry experience in clinical development. At Berlex, Rios was responsible for U.S. clinical development operations and oversaw the efforts of a 30 member staff that led to the filing of the biologics license application with the U.S. Food and Drug Administration (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. ) for the blockbuster drug A blockbuster drug is a drug generating more than $1 billion of revenue for its owner each year. The search for blockbusters has been the foundation of the R&D strategy adopted by big pharmaceutical companies, but this looks set to change. Betaseron(R), interferon a-1b. Worldwide sales of Betaseron(R) (Betaferon(R) in Europe), exceed $650 million. Rios also oversaw the clinical affairs activities in the U.S. for Campath(R), a humanized monoclonal antibody monoclonal antibody, an antibody that is mass produced in the laboratory from a single clone and that recognizes only one antigen. Monoclonal antibodies are typically made by fusing a normally short-lived, antibody-producing B cell (see immunity) to a fast-growing for chronic lymphocytic leukemia chronic lymphocytic leukemia n. Abbr. CLL Lymphocytic leukemia occurring mainly in older adults, characterized by slow onset and gradual progression of symptoms. approved by the FDA in 2001. "Dr. Rios joins Dendreon at an important time as we continue our efforts to move closer to bringing our therapeutic prostate cancer prostate cancer, cancer originating in the prostate gland. Prostate cancer is the leading malignancy in men in the United States and is second only to lung cancer as a cause of cancer death in men. vaccine, Provenge(TM) -- currently in Phase III clinical development -- to market," said Mitchell, H. Gold, M.D., chief executive officer. "Israel has a long history of success in seeing products through the regulatory process and into the market. We are very fortunate to add Israel to our management team at this time, and his extensive clinical development experience will greatly benefit our company." Prior to joining Berlex in 1993, Rios served as director of anti-infective clinical research for Marion Merrell Dow, Inc. He also held various positions at Bristol-Myers Company, including director of clinical research. Rios completed a residency in internal medicine and an internship at Mount Sinai Hospital Mount Sinai Hospital can refer to:
Dendreon Corporation is a biotechnology company developing targeted therapies for cancer. Dendreon currently has multiple therapeutic vaccines in clinical trials and preclinical development. Dendreon's product pipeline also includes monoclonal antibodies and a pathway to small molecules. Dendreon has established important alliances with industry leaders Genentech, Inc. and Kirin Brewery Co., Ltd. For more information, visit www.dendreon.com. Except for historical information contained herein, this news release contains forward-looking statements that are subject to risks and uncertainties that may cause actual results to differ materially from the results discussed in the forward-looking statements, particularly those risks and uncertainties inherent in the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics. Factors that may cause such a difference include reliance on key employees, especially senior management, risks related to Dendreon's limited operating history, risks associated with completing Dendreon's clinical trials, the risk that the results of a clinical trial, including Phase III trials of Provenge, will not support applying for or approval of a biologics license by the FDA, the uncertainty of Dendreon's future access to capital, the risk that Dendreon may not secure or maintain relationships with collaborators, and dependence on intellectual property. Further information on the factors and risks that could affect Dendreon's business, financial condition and results of operations, are contained in Dendreon's public disclosure filings with the U.S. Securities and Exchange Commission (SEC), which are available at www.sec.gov. |
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