Uploaded by netgenpr on Nov 14, 2010
P>Interview with Mr. Jeff Davis, President & CEO of Access Pharmaceuticals, Inc. (OTCBB: ACCP). Mr. Davis discusses the recent announcement of commencement of ProLindac Phase 2 Combination Clinical Trials. About Access: Access Pharmaceuticals, Inc. is an emerging biopharmaceutical company that develops and commercializes proprietary products for the treatment and supportive care of cancer patients. Access' products include MuGard™[6] (www.mugard.com[7]), for the management of patients with mucositis, ProLindac™,[8] currently in Phase II clinical testing of patients with ovarian cancer, and Thiarabine[9], a new generation nucleoside analog which has demonstrated both pre-clinical and clinical activity in certain cancers. The company also has additional advanced drug-delivery technologies, including CobaCyte™-mediated targeted delivery[10] and CobOral-oral drug delivery[11], its proprietary nanopolymer delivery technology based on the natural vitamin B12 uptake mechanism. For additional information on Access Pharmaceuticals, please visit our website at www.accesspharma.com[12]. This video blog contains certain statements that are forward-looking within the meaning of Section 27a of the Securities Act of 1933, as amended, and that involve risks and uncertainties. These statements include those relating to: our cash burn rate, clinical trial plans and timelines and clinical results for ProLindac, MuGard, Thiarabine and Cobalamin and other product candidates, our ability to achieve clinical and commercial success and our ability to successfully develop marketed products. These statements are subject to numerous risks, including but not limited Access' need to obtain additional financing in order to continue the clinical trial and operations and to the risks detailed in Access' Annual Reports on Form 10-K and other reports filed by Access with the Securities and Exchange Commission.
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