www.biocompatibles.com
Biocompatibles International plc is a leading company in the field of drug-device combination products. The Oncology Products Division conducts the marketing of Biocompatibles’ approved oncology products. These include products that are used for the treatment of primary liver cancer (HCC), liver metastases from colorectal cancer and prostate cancer. Our R&D Facilities are engaged in licensing and in new product development for oncology, stroke, and diabetes and obesity. We have collaborative agreements with AstraZeneca, Bayer Healthcare Pharmaceuticals Inc. and Medtronic Inc.
Biocompatibles reports positive results from liver cancer patient trial
Biocompatibles International PLC (LSE: BII) said a trial of its drug-eluting bead in primary liver cancer patients showed a tumour response rate of 90 percent at six months and adverse events within expected limits.
The trial was conducted at Johns Hopkins University School of Medicine in Baltimore, Maryland, under Professor Jean-Francois Geschwind, Professor of Radiology, Surgery and Oncology. It involved 20 patients with hepatocellular carcinoma, or HCC.
Professor Geschwind is now recruiting patients in a single arm Phase II trial evaluating the potential usefulness of sorafenib in conjunction with treatment with drug-eluting bead in 50 patients with HCC. Four patients have been treated and it is expected that preliminary data will be presented during the course of 2009. This trial is part of a clinical collaboration agreement between Biocompatibles and Bayer Pharmaceuticals Inc.
He is also recruiting patients in a 30 patient single arm trial evaluating the potential usefulness of the drug-eluting beads in patients with Neuroendocrine Metastases in the liver.
Professor Robert Martin, Associate Professor of Surgery in the Division of Surgical Oncology at the University of Louisville, has initiated a randomised trial for the evaluation of the Drug-Eluting Beads in hepatic colorectal metastases for patients who are not eligible for surgical resection (first line patients). The trial was announced mid-April 2009 and is known as PARAGON Louisville.
Professor Wells Messersmith, Associate Professor, Division of Medical Oncology, University of Colorado Cancer Center, Denver, CO, is recruiting patients with hepatic colorectal metastases who have failed one line of drug therapy (second line patients). This trial is known as PARAGON 1.
Biocpompatibles chief executive Crispin Simon said: "Our drug-eluting bead products are now routinely used in more than 35 countries; but we are maintaining our commitment to assembling definitive evidence in support of this evolution in clinical practice."
















