The Contractor shall develop a Phase I protocol design to evaluate the combination of an anti-GD3 antibody and either a biologic, such as recombinant and/or natural interferon, or cytoreductive agent in patients with melanoma.
Bajorin, D F; Chapman, P B; Wong, G et al. (1990) Phase I evaluation of a combination of monoclonal antibody R24 and interleukin 2 in patients with metastatic melanoma. Cancer Res 50:7490-5 |