Animal Studies Demonstrate the Importance Pro-Pharmaceuticals' DAVANAT Played in Significantly Increasing the Anti-Cancer Efficacy of 5-Fluorouracil.Business Editors/Health/Medical Writers BIOWIRE2K NEWTON, Mass.--(BUSINESS WIRE)--Sept. 16, 2003 Findings From Independent Studies Published in Peer-Reviewed Journal Preclinica(TM) Pro-Pharmaceuticals, Inc. (AMEX AMEX See: American Stock Exchange : PRW "Parents are watching." See digispeak. ), a developer of novel cancer therapeutics, today announced the results of animal studies that demonstrate the importance of the role DAVANAT(TM) played in significantly increasing the efficacy of 5-Fluorouracil (5-FU), a commonly used chemotherapy drug. The results were published in the September/ October issue of peer-reviewed journal peer-reviewed journal Refereed journal Academia A professional journal that only publishes articles subjected to a rigorous peer validity review process. Cf Throwaway journal. Preclinica(TM) (vol. 1, No. 4, pp. 175 -186). "The three separate, independent studies were conducted by two laboratories involving mice bearing human colon tumors (COLO Colo Colorado (old style state abbreviation) COLO Columbus, Ohio COLO Co-Location COLO Colonial National Historic Park (US National Park Service) COLO Cost Of Living Option 205 and HT-29)," said Eliezer Zomer, Pro-Pharmaceuticals' Vice President of Product Development. "The principal results of the studies demonstrate that DAVANAT(TM), when co-administered with 5-FU (DAVANAT(TM)-1), enhances the efficacy of 5-FU by further decreasing tumor growth rate by 42% to 140% as compared to 5-FU alone." "We undertook independent animal studies to test a potential change in the therapeutic efficacy of DAVANAT(TM) in a combination with 5-FU, which decreased toxicity of the drug in healthy animals," said Anatole Klyosov, Pro-Pharmaceuticals' Chief Scientist. "Results of the studies demonstrate that DAVANAT(TM) also increased the efficacy of 5-FU in a dose response matter, when administered into cancer-carrying animals. These findings support our belief that our technology can increase the human body's tolerance to toxic chemo cheĀ·mo n. Chemotherapy or a chemotherapeutic treatment. drugs by targeting their delivery to tumor-bearing cells." "The results are a clear indication of the power and efficacy of our platform technology and demonstrate the potential for a paradigm shift A dramatic change in methodology or practice. It often refers to a major change in thinking and planning, which ultimately changes the way projects are implemented. For example, accessing applications and data from the Web instead of from local servers is a paradigm shift. See paradigm. in the way drugs are designed," said David Platt
abbr. Food and Drug Administration FDA, n.pr See Food and Drug Administration. FDA, n.pr the abbreviation for the Food and Drug Administration. chemotherapy drugs and give them a targeting mechanism by utilizing our DAVANAT(TM) carbohydrate compound." The article, "Preclinical Studies preclinical studies, n.pl a term used to describe research done before a clinical study. May be laboratory or epidemiologic research. of Anticancer Efficacy of 5-Fluorouracil when Co-Administered with the 1,4-B(beta)-D-Galactomannan," is co-authored by the Company's Chief Scientist Anatole Klyosov, Vice President of Product Development, Eliezer Zomer 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. David Platt. Preclinica(TM) is a bi-monthly publication developed to bridge the critical gap between basic discovery and clinical trial. Designed to be the definitive forum for dialogue between academia, industry, and the FDA/NIH, Preclinica(TM) publishes peer-reviewed studies covering all aspects of pre-clinical research required before human clinical trials. Pro-Pharmaceuticals is conducting Phase I clinical trials Noun 1. phase I clinical trial - a clinical trial on a few persons to determine the safety of a new drug or invasive medical device; for drugs, dosage or toxicity limits should be obtained phase I of its DAVANAT(TM) -1 compound. In Phase I, the Company is evaluating the ability of patients to tolerate increasing doses of DAVANAT(TM) while receiving a stable dose of 5-FU for treatment of a variety of solid tumors that have not responded to accepted therapies. The Phase I study is also designed to define the dose-limiting toxicities of DAVANAT(TM) in combination with 5-FU. Pro-Pharmaceuticals, Inc. -- Advancing Drugs Through Glycoscience(TM) Pro-Pharmaceuticals, founded in 2000 and headquartered in Newton, MA, is a drug development company commercializing a new generation of anti-cancer treatments using carbohydrate molecules to upgrade the safety and efficacy of anti-cancer agents. The Company is a leader in the use of structure-based drug design; an approach to drug discovery that integrates advanced biology and chemistry. Additional information is available at www.pro-pharmaceuticals.com. FORWARD LOOKING STATEMENTS: Any statements in this press release about future expectations, plans and prospects for the Company, including without limitation statements containing the words "believes," "anticipates," "plans," "expects," "will" and similar expressions, constitute forward-looking statements as defined in the "safe harbor Safe Harbor 1. A legal provision to reduce or eliminate liability as long as good faith is demonstrated. 2. A form of shark repellent implemented by a target company acquiring a business that is so poorly regulated that the target itself is less attractive. " provisions of 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 of uncertainties and risks facing the Company, many of which are outside of the Company's control, future events could cause actual results to differ materially from those indicated by such statements. More information about those risks and uncertainties is contained and discussed in the "Plan of Operations" and "Risk Factors" sections of the Company's most recent quarterly or annual report and in the Company's other reports filed with the Securities and Exchange Commission. The forward-looking statements herein represent the Company's views as of the date of this press release and should not be relied upon to represent the Company's views as of a subsequent date. While the Company anticipates that subsequent events may cause the Company's views to change, the Company disclaims any obligation to update such forward-looking statements. |
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