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BioSphere to test Avastin with chemoembolization
By Elaine Rigoli
Tampa, Fla., June 13 - BioSphere Medical, Inc. said Tuesday that it is participating in a phase 2, single-arm clinical study to treat patients with primary liver cancer starting this month at The Johns Hopkins University School of Medicine.
The 30-patient, two-year study will combine Avastin (bevacizumab) with chemoembolization therapy using BioSphere's patented embosphere microspheres.
Participants will receive Avastin intravenously one week before and two weeks after undergoing a chemoembolization procedure.
The study is designed to study the safety and efficacy of combining chemoembolization with Avastin in patients with advanced liver cancer, according to a news release.
Avastin is a therapeutic monoclonal antibody designed to inhibit Vascular Endothelial Growth Factor, a protein that plays an important role in angiogenesis, the formation of tumor blood vessel networks in response to injury or interference, such as a chemoembolization procedure. In order to grow or spread, tumors require a constant supply of oxygen and nutrients that the blood vessel networks supply.
BioSphere Medical, a medical device company based in Rockland, Mass., develops minimally invasive diagnostic and therapeutic applications.
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