IP Library Granted Patent US 11,253,609
Granted Patent B2
US 11,253,609 · App. 16/489,569 · Granted Feb 22, 2022

Glycan-interacting compounds and methods of use

Inventors: Daniel T. Dransfield (Hanson, MA); Jillian M. Prendergast (Maynard, MA); David A. Eavarone (North Quincy, MA)
Assignee: Seagen Inc.
A61K47/6851A61K9/0019A61K31/337A61K31/44A61K31/4745A61K31/506A61K31/513A61K31/519A61K31/7068A61K33/243A61K38/08A61K39/3955A61K47/6817A61K47/6889A61P35/00C07K16/3076A61K2039/505A61K2039/545C07K2317/24C07K2317/73C07K2317/92
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Quick Facts
Patent No.
US 11,253,609
App. No.
16/489,569
Granted
Feb 22, 2022
Kind
B2
Abstract

Methods of treating cancer are provided that include administering glycan-interacting antibodies. Included are anti-sialyl Tn antigen antibodies and related compositions and formulations suitable to achieve desirable bioactivity, bioavailability, and toxicity levels.

Claims (13)

1. A method of treating platinum refractory cancer comprising administering to a subject with platinum refractory cancer an antibody-drug conjugate, wherein the antibody-drug conjugate comprises an antibody that binds sialyl Tn antigen (STn) conjugated to a cytotoxic agent, wherein the antibody comprises (a) a heavy chain variable domain (VH) comprising the amino acid sequence of SEQ ID NO: 7 and a light chain variable domain (VL) comprising the amino acid sequence of SEQ ID NO: 8; (b) a VH comprising the amino acid sequence of SEQ ID NO: 9 and a VL comprising the amino acid sequence of SEQ ID NO: 10; or (c) a VH comprising the amino acid sequence of SEQ ID NO: 11 and a VL comprising the amino acid sequence of SEQ ID NO: 12.

2. The method of claim 1 , wherein the cytotoxic agent is selected from an auristatin, a maytansine, a tubulysin, a vinca alkaloid, a pyrrolobenzodiazepine dimer, a camptothecin, a duocarmycin, an amanitin, a phosphoinositide 3-kinase (PI3K) inhibitor, and a mitogen-activated protein kinase kinase (MEK) inhibitor.

3. The method of claim 1 , wherein the cytotoxic agent is monomethyl auristatin E (MMAE).

4. The method of claim 3 , wherein the antibody is conjugated to said cytotoxic agent via a linker.

5. The method of claim 4 , wherein the linker comprises one or more polymers selected from a poly(ethylene glycol) (PEG), a poly(N-(2-hydroxypropyl)methacrylamide) (polyHPMA), a poly(α-amino acid), a carbohydrate polymer, a glycopolysaccharide, a glycolipid, a glycoconjugate, a polyglycerol, a polyvinyl alcohol, a poly(acrylic acid), a polyketal, a polyacetal, and a poly(1-hydroxymethylethylene hydroxymethylformal) (PHF).

6. The method of claim 4 , wherein the linker comprises valine-citrulline.

7. The method of claim 6 , wherein the antibody comprises a heavy chain variable domain (VH) comprising the amino acid sequence of SEQ ID NO: 7 and a light chain variable domain (VL) comprising the amino acid sequence of SEQ ID NO: 8.

8. The method of claim 1 , wherein the platinum refractory cancer is resistant to a platinum-based agent selected from cisplatin, oxaliplatin, and carboplatin.

9. The method of claim 7 , wherein the platinum refractory cancer is resistant to a platinum-based agent selected from cisplatin, oxaliplatin, and carboplatin.

10. The method of claim 1 , wherein the platinum refractory cancer is selected from breast cancer, ovarian cancer, melanoma, colon cancer, liver cancer, lung cancer, bladder cancer, cervical cancer, stomach cancer, and prostate cancer.

11. The method of claim 1 , wherein the platinum refractory cancer is selected from ovarian cancer and lung cancer.

12. The method of claim 7 , wherein the platinum refractory cancer is selected from breast cancer, ovarian cancer, melanoma, colon cancer, liver cancer, lung cancer, bladder cancer, cervical cancer, stomach cancer, and prostate cancer.

13. The method of claim 7 , wherein the platinum refractory cancer is selected from ovarian cancer and lung cancer.

Assignments (1)
CHANGE OF NAME Recorded Oct 21, 2020
From: SEATTLE GENETICS, INC.
To: SEAGEN INC.
Reel/Frame 054174/0595 →