Granted Patent B2

US 12,377,144 · App. 17/686,238 · Granted Aug 5, 2025

Inventors: Jean-Marie Cuillerot (Somerville, MA); Mark DeRose (Wilmington, MA); Christopher Ryan Morgan (Southborough, MA); Michael C. Naill (Stow, MA); Avni Shah (Framingham, MA)

Assignee: Dragonfly Therapeutics, Inc.

A61K39/39591A61K31/138A61K31/167A61K31/573A61K39/3955A61K39/39558A61K47/22A61K47/26A61P1/00A61P35/00A61P35/04C07K16/283C07K16/2851C07K16/32A61K2039/505A61K2039/54A61K2039/545C07K2317/31

Abstract

Claims (39)

1. A method of treating a breast cancer, the method comprising administering a therapeutically effective amount of a multi-specific binding protein to a subject in need thereof,

wherein the breast cancer is positive for a hormone receptor and:

(i) has a HER2 expression level scored as 2+ as determined by immunohistochemistry (IHC), but not ERBB2 gene amplification as determined by an in situ hybridization (ISH) assay, or

(ii) has a HER2 expression level scored as 1+ as determined by IHC;

wherein the multi-specific binding protein comprises:

(a) a first antigen-binding site that binds NKG2D;

(b) a second antigen-binding site that binds HER2; and

(c) an antibody Fc domain or a portion thereof sufficient to bind CD16, or a third antigen-binding site that binds CD16.

2. The method of claim 1 , wherein the hormone receptor is estrogen receptor, progesterone receptor, or both.

3. The method of claim 1 , wherein the multi-specific binding protein is administered to the subject in an initial four-week treatment cycle on Day 1, Day 8, and Day 15, but not Day 22.

4. The method of claim 3 , further comprising administering to the subject, after the initial treatment cycle, the multi-specific binding protein in one or more subsequent four-week treatment cycles, wherein the multi-specific binding protein is administered on Day 1 and Day 15 in each subsequent treatment cycle.

5. The method of claim 4 , wherein each of the doses comprises the multi-specific binding protein at an amount selected from the group consisting of 5 mg/kg, 10 mg/kg, 15 mg/kg, and 20 mg/kg, administered by intravenous infusion.

6. The method of claim 3 , further comprising administering to the subject, on Day 1 of the initial four-week treatment cycle, a therapeutically effective amount of a corticosteroid to reduce one or more infusion-related reactions to the multi-specific binding protein.

7. The method of claim 6 , wherein the corticosteroid is a glucocorticoid selected from the group consisting of methylprednisolone, dexamethasone, hydrocortisone, prednisone, prednisolone, fluticasone, flumethasone, fluocinolone, budesonide, beclomethasone, ciclesonide, cortisone, triamcinolone, betamethasone, deflazacort, difluprednate, loteprednol, paramethasone, tixocortol, and pharmaceutically acceptable salts thereof.

8. The method of claim 6 , wherein the infusion-related reactions comprise cytokine release syndrome, anaphylaxis, chills, fever, hypotension, hypertension, rigors, headache, dizziness, itching, sore throat, laryngeal edema, angioedema, flushing, rash, bronchospasm, tachycardia, bradycardia, auricular fibrillation, hypoxia, dyspnea, respiratory distress, chest tightness, nausea, vomiting, shivering, tremors, pain, tiredness, insomnia, asthenia, hypersensitivity, and/or diarrhea.

9. The method of claim 1 , further comprising administering to the subject a chemotherapy.

10. The method of claim 1 , wherein the first antigen-binding site that binds NKG2D comprises:

(a) a heavy chain variable domain (VH) comprising complementarity-determining region 1 (CDR1), complementarity-determining region 2 (CDR2), and complementarity-determining region 3 (CDR3) sequences represented by the amino acid sequences of SEQ ID NOs: 168, 96, and 188, respectively; and

(b) a light chain variable domain (VL) comprising CDR1, CDR2, and CDR3 sequences represented by the amino acid sequences of SEQ ID NOs: 99, 100, and 101, respectively.

11. The method of claim 10 , wherein

(a) the VH comprises CDR1, CDR2, and CDR3 sequences represented by the amino acid sequences of SEQ ID NOs: 168, 96, and 169, respectively; and

(b) the VL comprises CDR1, CDR2, and CDR3 sequences represented by the amino acid sequences of SEQ ID NOs: 99, 100, and 101, respectively.

12. The method of claim 11 , wherein the VH comprises an amino acid sequence at least 90% identical to SEQ ID NO:94, and the VL comprises an amino acid sequence at least 90% identical to SEQ ID NO:98.

13. The method of claim 1 , wherein the second antigen-binding site that binds HER2 comprises:

(a) a VH comprising CDR1, CDR2, and CDR3 sequences represented by the amino acid sequences of SEQ ID NOs: 115, 116, and 117, respectively; and

(b) a VL comprising CDR1, CDR2, and CDR3 sequences represented by the amino acid sequences of SEQ ID NOs: 119, 120, and 121, respectively.

14. The method of claim 13 , wherein the VH comprises an amino acid sequence at least 90% identical to SEQ ID NO:195, and the VL comprises an amino acid sequence at least 90% identical to SEQ ID NO:196.

15. The method of claim 1 , wherein the first antigen-binding site that binds NKG2D is a Fab, and the second antigen-binding site that binds HER2 is an scFv.

16. The method of claim 15 , wherein element (c) of the multi-specific binding protein is an antibody Fc domain, wherein the antibody Fc domain comprises a first antibody Fc sequence linked to a C-terminus of a heavy chain portion of the first antigen-binding site and a second antibody Fc sequence linked to a C-terminus of the second antigen-binding site via a hinge comprising Ala-Ser, and wherein the first and second antibody Fc sequences comprise different mutations that promote heterodimerization.

17. The method of claim 16 , wherein the first antibody Fc sequence is a human IgG1 Fc sequence comprising K360E and K409W substitutions, and the second antibody Fc sequence is a human IgG1 Fc sequence comprising Q347R, D399V, and F405T substitutions, according to the EU numbering system.

18. The method of claim 1 , wherein the multi-specific binding protein comprises:

(a) a first polypeptide comprising the amino acid sequence of SEQ ID NO:141;

(b) a second polypeptide comprising the amino acid sequence of SEQ ID NO: 140; and

(c) a third polypeptide comprising the amino acid sequence of SEQ ID NO:142.

19. The method of claim 5 , wherein each of the doses in the one or more subsequent treatment cycles comprises 10 mg/kg of the multi-specific binding protein administered by intravenous infusion.

20. The method of claim 19 , wherein the multi-specific binding protein comprises:

(a) a first polypeptide comprising the amino acid sequence of SEQ ID NO:141;

(b) a second polypeptide comprising the amino acid sequence of SEQ ID NO:140; and

(c) a third polypeptide comprising the amino acid sequence of SEQ ID NO:142.

Assignments (1)

Continuity (2)

References Cited (400)