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US 2025/0026837 A1Published application
MIC Antibodies and Binding Agents and Methods of Using the Same
AssigneeCancure Limited
InventorJennifer Wu
Life of this patent
Estimating the term…
Abstract
The present invention provides MIC antibodies, antigen binding portions thereof and MIC binding agents thereof for use in the treatment of cancer.
Claims41
1-76.(canceled)
A method of treating a MIC+ cancer, comprising administering to a subject in need thereof:
- a therapeutically effective amount of an isolated monoclonal antibody or antigen-binding portion thereof that specifically binds MIC, wherein the antibody or antigen-binding portion thereof each comprises a heavy chain variable (VH) region and a light chain variable (VL) region, wherein the VH region comprises a complementarity determining region HCDR1 sequence having the amino acid sequence set forth in SEQ ID NO:11, a HCDR2 having the amino acid sequence set forth in SEQ ID NO:12, and a HCDR3 having the amino acid sequence set forth in SEQ ID NO:13, and wherein the VL region comprises a LCDR1 sequence having the amino acid sequence set forth in SEQ ID NO:14, a LCDR2 having the amino acid sequence set forth in SEQ ID NO:15, and a LCDR3 having the amino acid sequence set forth in SEQ ID NO:16, wherein the VH region comprises an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO:
- 1, and the VL region comprises an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO:
- 2.
A method of treating a cancer, comprising administering to a subject in need thereof:
- a therapeutically effective amount of an isolated monoclonal antibody or antigen-binding portion thereof that specifically binds MIC, wherein the antibody or antigen-binding portion thereof each comprises a heavy chain variable (VH) region and a light chain variable (VL) region, wherein the VH region comprises a complementarity determining region HCDR1 sequence having the amino acid sequence set forth in SEQ ID NO:11, a HCDR2 having the amino acid sequence set forth in SEQ ID NO:12, and a HCDR3 having the amino acid sequence set forth in SEQ ID NO:13, and wherein the VL region comprises a LCDR1 sequence having the amino acid sequence set forth in SEQ ID NO:14, a LCDR2 having the amino acid sequence set forth in SEQ ID NO:15, and a LCDR3 having the amino acid sequence set forth in SEQ ID NO:16, wherein the VH region comprises an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO:
- 1, and the VL region comprises an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO:
- 2;
- and
- an adoptive cell therapy.
2 more elements
Dependencies are inferred from the claim text.