FDA grants IND application for use of DAVANAT
Pro-Pharmaceuticals Inc., on the 30th of August, 2008, announced that the U.S. Food and Drug Administration (FDA) has granted an Investigational New Drug (IND) application for use of DAVANATĀ® in combination with 5-FU to treat a patient of breast cancer at the Brown Cancer Center in Louisville, Kentucky. Also, DAVANAT is being administered in Phase II clinical trials for first-line treatment of colorectal and biliary cancer patients. Studies showed that DAVANATĀ®, when given along with chemotherapy, reduced tumor growth and toxicity considerably in mice implanted with metastatic human breast cancer. It also lowered the levels of side effects.

According to the Wichita Eagle, the operating funds of the Kansas