On 1/28/2007 Honolulu wrote:
The Mayo Clinic, barnes Jewish Hospital/Washington University in St. Louis and, I believe the University of Nebraska are doing treatment of this cancer with new techniques. Have your doctor contact those facilities (at barnes it Dr. William Chapman). Also, the University of Michigan just is beginning a Clinical trial of Davanat with (I think) 5FU Chemo on this cholangiocarcinoma (Dr. Zalupsky). Good luck. You must be aggressive at finding the new treatments.
Here is an added quote on DAVANAT.
Tue Jan 23 06:21:16 2007 (Pro-Pharmaceuticals, Inc.)
Pro-Pharmaceuticals Announces Dosing of Patients with DAVANAT(R) in Phase II, First Line, Advanced Biliary Cancer Clinical Trial
NEWTON, Mass.--(BUSINESS WIRE)--Pro-Pharmaceuticals, Inc. (Amex:PRW - News), a developer of novel carbohydrate compounds, today announced the dosing of patients in its Phase II, first line, biliary cancer trial. The Phase II trial is an open-label, multi-center trial of DAVANAT® with 5-Fluorouracil (5-FU) to treat patients with advanced bile duct and gall bladder cancer.
"Our excellent Phase I/II results show DAVANAT®, when co-administered with 5-FU, stabilized the disease and improved the quality of life for many of the end-stage cancer patients," said David Platt, Ph.D., President and Chief Executive Officer, Pro-Pharmaceuticals, Inc. "When we combine the very positive results from those trials, with the data expected from the ongoing biliary and colorectal first line cancer trials, we will prove the clinical benefit of DAVANAT® to treat cancer patients.
"In addition, we continue discussions with pharmaceutical companies who are evaluating our technology. Our goal is to facilitate collaborations that will enable us to get our compounds to market quickly in multiple indications and modalities," stated Dr. Platt.
Phase II, First Line, Biliary Cancer Trial
The Company is actively recruiting and dosing patients in a Phase II study of DAVANAT® with 5-FU for first line treatment of advanced biliary cancer. The primary objectives of the trial are a partial or complete tumor response and stable disease. Secondary outcomes include progression-free survival and quality of life. The multi-center, open-label study will evaluate up to 42 patients treated with DAVANAT® and 5-FU for at least two cycles or to disease progression. An end stage, cholangiocarcinoma (bile duct) patient from the Phase I, all solid tumors, cancer trial remained on study for 13 months, far exceeding expectations. Treatment of biliary cancer may represent an opportunity for orphan drug status approval.
Two clinical sites are currently recruiting patients in the biliary cancer trial: University of Michigan, Comprehensive Cancer Center in Ann Arbor, Michigan, and Barrett Cancer Center in Cincinnati, Ohio. The Company expects additional sites to become active shortly. Additional information on the this trial and the Company's Phase II, first line, colorectal cancer clinical trial as well as participating sites, can be found at www.clinicaltrials.gov website, key word: DAVANAT®.
About DAVANAT®
DAVANAT®, the Company's lead drug candidate, is a carbohydrate (polysaccharide) polymer composed of mannose and galactose. The Company believes DAVANAT®'s mechanism of action is based upon binding to lectins on the cell surface. Lectins are carbohydrate binding proteins found in increased amounts on cell surfaces. DAVANAT®, when injected into humans, recognizes and attaches to lectins. It is theorized that DAVANAT® targets specific lectin receptors (Galectins) that are over-expressed on cancer cells. Current research indicates that Galectins affect cell development and play important roles in cancer, including tumor cell survival, angiogenesis and tumor metastasis. This form of targeted delivery may allow for higher doses of chemotherapy administration with no increase in toxicity.
Pro-Pharmaceuticals, Inc. - Advancing Drugs Through Glycoscience®
Pro-Pharmaceuticals is a development stage pharmaceutical company engaged in the discovery, development and commercialization of carbohydrate-based therapeutic compounds for advanced treatment of cancer, liver, microbial, cardiovascular and inflammatory diseases. Initially, the product pipeline is principally focused on increasing the efficacy and decreasing the toxicity of approved chemotherapy drugs. The Company has been conducting clinical and pre-clinical studies with its lead compound, DAVANAT®, in combination with 5-FU, leucovorin, irinotecan, doxorubicin, oxaliplatin, paclitaxel, cisplatin, and bevacizumab (Avastin®). Results show that DAVANAT® exhibits a broad spectrum of activity with tested drugs. The Company is developing other carbohydrate-based therapeutic compounds that are currently in the pre-clinical stage of development. Founded in 2000, the Company is headquartered in Newton, Mass. Additional information is available at www.pro-pharmaceuticals.com.
"Our excellent Phase I/II results show DAVANAT®, when co-administered with 5-FU, stabilized the disease and improved the quality of life for many of the end-stage cancer patients," said David Platt, Ph.D., President and Chief Executive Officer, Pro-Pharmaceuticals, Inc. "When we combine the very positive results from those trials, with the data expected from the ongoing biliary and colorectal first line cancer trials, we will prove the clinical benefit of DAVANAT® to treat cancer patients.
"In addition, we continue discussions with pharmaceutical companies who are evaluating our technology. Our goal is to facilitate collaborations that will enable us to get our compounds to market quickly in multiple indications and modalities," stated Dr. Platt.
Phase II, First Line, Biliary Cancer Trial
The Company is actively recruiting and dosing patients in a Phase II study of DAVANAT® with 5-FU for first line treatment of advanced biliary cancer. The primary objectives of the trial are a partial or complete tumor response and stable disease. Secondary outcomes include progression-free survival and quality of life. The multi-center, open-label study will evaluate up to 42 patients treated with DAVANAT® and 5-FU for at least two cycles or to disease progression. An end stage, cholangiocarcinoma (bile duct) patient from the Phase I, all solid tumors, cancer trial remained on study for 13 months, far exceeding expectations. Treatment of biliary cancer may represent an opportunity for orphan drug status approval.
Two clinical sites are currently recruiting patients in the biliary cancer trial: University of Michigan, Comprehensive Cancer Center in Ann Arbor, Michigan, and Barrett Cancer Center in Cincinnati, Ohio. The Company expects additional sites to become active shortly. Additional information on the this trial and the Company's Phase II, first line, colorectal cancer clinical trial as well as participating sites, can be found at www.clinicaltrials.gov website, key word: DAVANAT®.
About DAVANAT®
DAVANAT®, the Company's lead drug candidate, is a carbohydrate (polysaccharide) polymer composed of mannose and galactose. The Company believes DAVANAT®'s mechanism of action is based upon binding to lectins on the cell surface. Lectins are carbohydrate binding proteins found in increased amounts on cell surfaces. DAVANAT®, when injected into humans, recognizes and attaches to lectins. It is theorized that DAVANAT® targets specific lectin receptors (Galectins) that are over-expressed on cancer cells. Current research indicates that Galectins affect cell development and play important roles in cancer, including tumor cell survival, angiogenesis and tumor metastasis. This form of targeted delivery may allow for higher doses of chemotherapy administration with no increase in toxicity.
Pro-Pharmaceuticals, Inc. - Advancing Drugs Through Glycoscience®
Pro-Pharmaceuticals is a development stage pharmaceutical company engaged in the discovery, development and commercialization of carbohydrate-based therapeutic compounds for advanced treatment of cancer, liver, microbial, cardiovascular and inflammatory diseases. Initially, the product pipeline is principally focused on increasing the efficacy and decreasing the toxicity of approved chemotherapy drugs. The Company has been conducting clinical and pre-clinical studies with its lead compound, DAVANAT®, in combination with 5-FU, leucovorin, irinotecan, doxorubicin, oxaliplatin, paclitaxel, cisplatin, and bevacizumab (Avastin®). Results show that DAVANAT® exhibits a broad spectrum of activity with tested drugs. The Company is developing other carbohydrate-based therapeutic compounds that are currently in the pre-clinical stage of development. Founded in 2000, the Company is headquartered in Newton, Mass. Additional information is available at www.pro-pharmaceuticals.com.