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ARIUS to Present at American Association for Cancer Research Annual,Meeting

ognizes an epitope of CD44 that is highly expressed in liver cancers. Abstract 662, Section 27, Board 15, Sunday, Apr 15, 8AM - 12PM

ARH460-16-2, a functional antibody that targets CD44, has previously been shown to have anti-tumor and survival benefits in animal models of breast and prostate cancers. New immunohistochemistry (IHC) studies demonstrated high levels of ARH460-16-2 binding to primary liver tumors: 43% (21/49). The antibody also bound more frequently to metastatic than to primary hepatocellular carcinomas, 88% (7/8) versus 30% (11/37), and there was a trend towards higher binding in advanced AJCC stages in comparison with earlier stages: 0% (stage I), 12% (stage II), 50% (stage III) and 75% (stage IV). In vivo studies are currently under way, to assess the therapeutic effect of this antibody in an in vivo model of metastatic hepatocellular carcinoma.

Functional antibodies targeting Trop-2 demonstrate in vivo efficacy in human pancreatic and other solid tumor xenograft models. Abstract 904, Section 5, Board 3, Sunday, Apr 15, 1PM - 5PM

Two monoclonal antibodies directed against Trop-2, AR47A6.4.2 and AR52A301.5, have been independently generated which, in in vitro assays, induce cytotoxicity in pancreatic, colon, lung and ovarian cancer cell lines.

Experiments conducted using the human pancreatic BxPC-3 xenograft model demonstrated that treatment with these antibodies resulted in tumor growth inhibition in both prophylactic and established models. The in vivo anti-tumor efficacy of these antibodies was examined in models of other solid tumor cancer indications, and the anti-tumor effect in human pancreatic cancer was substantiated by a second model of human pancreatic cancer. With the aim of bringing these antibodies to the clinic, the selection of an animal model for toxicology studies was undertaken. Results from these studies have
demonstrated a very similar expression pattern between hum
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