Our lead candidate, IGN002, comprises an anti-CD20 monoclonal antibody
attached to IFN through stable peptide linker system. CD20 is expressed on
Non-Hodgkin lymphoma and other B cell driven hematologic malignancies. We
have generated substantial preclinical data with IGN002, including data
demonstrating that the targeting ability of IGN002 results in up to 100-fold
higher than non-targeted IFN. Further, IGN002 also shows remarkable efficacy
in rituximab resistant tumor models. These preclinical data demonstrate that
IGN002 effectively targets and acts locally CD20- positive tumors.
IGN001:
Our second candidate, IGN001, comprises an anti-Her2 monoclonal antibody
attached to IFN through stable peptide linker system. Her2 is expressed on
breat cancer and other malignancies. We are in early stages of generating
preclinical data with IGN001.
IGN004:
Our candidate, IGN004, comprises an monoclonal antibody
against a novel target attached to IFN through stable peptide linker system.
This target is expressed on
multiple solid tumors and melanomas. We are in early stages of generating
preclinical data with IGN004.
IGN005:
Our IGN005 candidate comprises an monoclonal antibody
directed towards a well validated AML target attached to IFN through stable peptide linker system.
This target is expressed on
AML and other leukemias. We are in early stages of generating
preclinical data with IGN005.