ADAM17 binding molecules and uses thereof

Patent metadata

Field	Value
Publication number	US-12378321-B2
Application number	US-202017437065-A
Country	US
Kind code	B2
Filing date	Mar 7, 2020
Priority date	Mar 8, 2019
Publication date	Aug 5, 2025
Grant date	Aug 5, 2025

Abstract

The present invention provides various ADAM17 binding molecules (including antibodies and fragments thereof), compositions comprising such ADAM17 binding molecules, and methods of using such ADAM17 binding molecules and compositions, for example in inhibiting binding of ADAM17 to ADAM17 substrates (such as ErbB ligands), in inhibiting the proliferation of cancer cells, and in treating cancer.

First claim

The invention claimed is:

1. An isolated ADAM17 binding molecule comprising one of:
(a) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 17, a CDR H2 domain comprising SEQ ID NO. 18, and a CDR H3 domain comprising SEQ ID NO. 19, and
(ii) a light chain variable region comprising: a CDR L1 domain comprising SEQ ID NO. 20, a CDR L2 domain comprising SEQ ID NO. 21, a CDR L3 domain comprising SEQ ID NO. 22; or

(b) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 23, a CDR H2 domain comprising SEQ ID NO. 24, and a CDR H3 domain comprising SEQ ID NO. 25, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 26, a CDR L2 domain comprising SEQ ID NO. 27, a CDR L3 domain comprising SEQ ID NO. 28; or

(c) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 29, a CDR H2 domain comprising SEQ ID NO. 30, and a CDR H3 domain comprising SEQ ID NO. 31, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 32, a CDR L2 domain comprising SEQ ID NO. 33, a CDR L3 domain comprising SEQ ID NO. 34; or

(d) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 41, a CDR H2 domain comprising SEQ ID NO. 42, and a CDR H3 domain comprising SEQ ID NO. 43, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 44, a CDR L2 domain comprising SEQ ID NO. 45, a CDR L3 domain comprising SEQ ID NO. 46; or

(e) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 47, a CDR H2 domain comprising SEQ ID NO. 48, and a CDR H3 domain comprising SEQ ID NO. 49, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 50, a CDR L2 domain comprising SEQ ID NO. 51, a CDR L3 domain comprising SEQ ID NO. 52.

2. An isolated ADAM17 binding molecule according to claim 1 , comprising one of:
(a) (i) a heavy chain variable region comprising amino acids 25-139 of SEQ ID NO. 1, and
(ii) a light chain variable region comprising amino acids 21-136 of SEQ ID NO. 2; or

(b) (i) a heavy chain variable region comprising amino acids 25-139 of SEQ ID NO. 3, and
(ii) a light chain variable region comprising amino acids 21-136 of SEQ ID NO. 4; or

(c) (i) a heavy chain variable region comprising amino acids 25-139 of SEQ ID NO. 5, and
(ii) a light chain variable region comprising amino acids 21-136 of SEQ ID NO. 6; or

(d) (i) a heavy chain variable region comprising amino acids 25-139 of SEQ ID NO. 7, and
(ii) a light chain variable region comprising amino acids 21-136 of SEQ ID NO. 8; or

(e) (i) a heavy chain variable region comprising amino acids 25-139 of SEQ ID NO. 9, and
(ii) a light chain variable region comprising amino acids 21-136 of SEQ ID NO. 10.

3. An isolated ADAM17 binding molecule according to claim 1 , comprising one of:
(a) (i) a heavy chain comprising SEQ ID NO. 1 and
(ii) a light chain comprising SEQ ID NO. 2: or

(b) (i) a heavy chain comprising SEQ ID NO. 3 and
(ii) a light chain comprising SEQ ID NO. 4; or

(c) (i) a heavy chain comprising SEQ ID NO. 5 and
(ii) a light chain comprising SEQ ID NO. 6; or

(d) (i) a heavy chain comprising SEQ ID NO. 7 and
(ii) a light chain variable region comprising SEQ ID NO. 8; or

(e) (i) a heavy chain comprising SEQ ID NO. 9 and
(ii) a light chain comprising SEQ ID NO. 10.

4. An ADAM17 binding molecule according to claim 1 , wherein the binding molecule is an antibody.

5. An ADAM17 binding molecule according to claim 4 , wherein the antibody is a fully human antibody, a chimeric antibody, a monoclonal antibody, a polyclonal antibody, a bi-specific antibody, or a multi-specific antibody.

6. An ADAM 17 binding molecule according to claim 1 , wherein the binding molecule is a Fv, a Fab, a F(ab′)2, a Fab′, a dsFv fragment, a single chain Fv (scFV), an sc(Fv)2, a disulfide-linked (dsFv), a diabody, a triabody, a tetrabody, a minibody, or a single chain antibody.

7. A composition comprising an ADAM17 binding molecule according to claim 1 .

8. An isolated nucleic acid molecule comprising a nucleotide sequence encoding an ADAM17 binding molecule according to claim 1 .

9. A vector comprising a nucleic acid molecule according to claim 8 .

10. A host cell comprising a nucleic acid molecule according to claim 8 .

11. A method for detecting ADAM17 in a sample, the method comprising (a) contacting a sample with an ADAM17 binding molecule according to claim 1 , and (b) detecting binding of the ADAM17 binding molecule to ADAM17, thereby detecting ADAM17 in the sample.

12. A method for inhibiting the proliferation of, or killing, tumor cells, the method comprising delivering to tumor cells an effective amount of an ADAM17 binding molecule comprising:
(A) (i) a heavy chain variable region comprising: a CDR HI domain comprising SEQ ID NO. 23, a CDR H2 domain comprising SEQ ID NO. 24, and a CDR H3 domain comprising SEQ ID NO. 25, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 26, a CDR L2 domain comprising SEQ ID NO. 27, a CDR L3 domain comprising SEQ ID NO: 28; or

(B) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 41, a CDR H2 domain comprising SEQ ID NO. 42, and a CDR H3 domain comprising SEQ ID NO. 43, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 44, a CDR L2 domain comprising SEQ ID NO. 45, a CDR L3 domain comprising SEQ ID NO. 46.

13. The method of claim 12 , wherein the tumor cells are selected from the group consisting of breast cancer cells, colon cancer cells, lung cancer cells, non-small cell lung cancer cells, brain cancer cells, glioma cells, glioblastoma cells, neuroblastoma cells, stomach cancer cells, pancreatic cancer cells, ovarian cancer cells, prostate cancer cells, and kidney cancer cells.

14. The method of claim 12 , wherein the tumor cells are triple-negative breast cancer cells.

15. The method of claim 12 , wherein the tumor cells are in vitro.

16. The method of claim 12 , wherein the tumor cells are in vivo.

17. A method of inhibiting a biological activity in cells or in a tissue, wherein the biological activity is selected from the group consisting of: (a) binding of ADAM17 to an ADAM17 substrate, (b) proteolytic cleavage of an ADAM17 substrate by ADAM17, (c) activation of an ADAM17 substrate, and (d), signaling by an ADAM17 substrate, wherein the method comprises delivering an effective amount of an ADAM17 binding molecule comprising:
(A) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 23, a CDR H2 domain comprising SEQ ID NO. 24, and a CDR H3 domain comprising SEQ ID NO. 25, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 26, a CDR L2 domain comprising SEQ ID NO. 27, a CDR L3 domain comprising SEQ ID NO: 28; or

(B) (i) a heavy chain variable region comprising: a CDR H1 domain comprising SEQ ID NO. 41, a CDR H2 domain comprising SEQ ID NO. 42, and a CDR H3 domain comprising SEQ ID NO. 43, and
(ii) a light chain variable region comprising: a CDR LI domain comprising SEQ ID NO. 44, a CDR L2 domain comprising SEQ ID NO. 45, a CDR L3 domain comprising SEQ ID NO. 46,
to cells or a tissue that expresses or contains ADAM17, thereby inhibiting the biological activity in the cells or tissue.

18. A method of treating cancer in a subject, the method comprising administering to a subject having cancer an effective amount o

Assignees

• Memorial Sloan Kettering Cancer Center
• Us Health
• Tri Inst Therapeutics Discovery Inst Inc

Inventors

• Nikolov Dimitar
• Saha Nayanendu
• Zhu Zhongyu
• Dimitrov Dimiter Stanchev
• Robev Dorothea
• White Thomas Edgeworth

Classifications

• A61K2039/505

  comprising antibodies · CPC title

• A61K39/00

  Medicinal preparations containing antigens or antibodies (materials for immunoassay G01N33/53) · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A01K2267/0331

  Animal model for proliferative diseases · CPC title

• A01K2227/105

  Murine · CPC title