IP Library Granted Patent US 12,600,763
Granted Patent B2
US 12,600,763 · App. 17/883,427 · Granted Apr 14, 2026

Compositions and methods for the delivery of therapeutic biologics for treatment of disease

Inventors: Paul Brown (Boston, MA); Tyler L Carter (Newburyport, MA); Lyndon Fitzgerald Charles, Jr. (Medford, MA); Chase Spenser Coffman (Newton, MA); Daniel Benjamin Dadon (East Boston, MA); Lisa Liu (Somerville, MA); Sadiqua Shadbar (Allston, MA); Chaitanya Sudrik (Stoneham, MA); Yi Tang (Medford, MA); Shankul Vartak (Cambridge, MA)
Assignee: Halozyme Hypercon, Inc.
C07K16/00A61K45/06
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Quick Facts
Patent No.
US 12,600,763
App. No.
17/883,427
Granted
Apr 14, 2026
Kind
B2
Abstract

The present disclosure provides compositions and methods for treating a disease or condition in a subject in need thereof, comprising administering to the subject a pharmaceutically effective amount of a composition comprising a plurality of particles comprising at least one therapeutic biologic suspended in a pharmaceutically acceptable liquid carrier.

Claims (18)

1 . A pharmaceutically effective composition comprising particles suspended in a carrier comprising fatty acid esters, wherein a plurality of the particles comprise at least one antibody or a fragment thereof, wherein the total weight percent of the at least one antibody or the fragment thereof in the plurality of particles is greater than 65%, and wherein the composition further comprises a hyaluronan degrading agent.

2 . The composition of claim 1 , wherein the carrier comprises fatty acid ethyl esters.

3 . The composition of claim 1 , wherein the carrier comprises ethyl oleate.

4 . The composition of claim 1 , wherein the particles have less than 10% aggregation of the at least one antibody or the fragment thereof.

5 . The composition of claim 1 , wherein the particles have less than 5% aggregation of the at least one antibody or the fragment thereof.

6 . The composition of claim 1 , wherein the particles have less than 3% aggregation of the at least one antibody or the fragment thereof.

7 . The composition of claim 1 , wherein the particles have a circularity from 0.80 to 1.00.

8 . The composition of claim 1 , wherein the particles have less than 3% residual moisture by weight.

9 . The composition of claim 1 , wherein the particles have greater than 70% of the at least one antibody or the fragment thereof by weight.

10 . The composition of claim 1 , wherein the particles have greater than 80% of the at least one antibody or the fragment thereof by weight.

11 . The composition of claim 1 , wherein the particles have less than 3% change in charge variants of the at least one antibody or the fragment thereof.

12 . The composition of claim 1 , wherein the particles further comprise at least one excipient selected from a carbohydrate, a pH adjusting agent, a salt, a chelator, a mineral, a polymer, a surfactant, a protein stabilizer, an emulsifier, an antiseptic, an amino acid, an antioxidant, a protein, an organic solvent, a paraben, a bactericide, a fungicide, a vitamin, a preservative, a nutrient media, analgesic, or a combination thereof.

13 . The composition of claim 1 , wherein the concentration of the at least one antibody or the fragment thereof in the composition is from 300 mg/mL to 650 mg/mL.

14 . The composition of claim 1 , wherein the concentration of the at least one antibody or the fragment thereof in the composition is from 400 mg/mL to 650 mg/mL.

15 . The composition of claim 1 , wherein the composition has a viscosity of less than 100 mPa·s.

16 . A pharmaceutically effective composition comprising particles suspended in a carrier comprising ethyl oleate, wherein a plurality of the particles comprise at least one antibody or fragment thereof, and have diameters in the range of 10 μm to 50 μm, wherein the total weight percent of the at least one antibody or fragment thereof in the plurality of particles is greater than 65%, wherein the concentration of the at least one antibody or the fragment thereof in the composition is from 300 mg/mL to 650 mg/mL, and wherein the composition further comprises a hyaluronan degrading agent.

17 . The composition of claim 1 , wherein the carrier comprises propylene glycol diesters.

18 . The composition of claim 1 , wherein the hyaluronan degrading agent is a hyaluronidase.

Assignments (2)
CHANGE OF NAME Recorded Feb 2, 2026
From: ELEKTROFI, INC.
To: HALOZYME HYPERCON, INC.
Reel/Frame 073662/0717 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2022
From: BROWN, PAUL; CARTER, TYLER L.; CHARLES, LYNDON FITZGERALD, JR.; COFFMAN, CHASE SPENSER; DADON, DANIEL BENJAMIN; LIU, LISA; SHADBAR, SADIQUA; SUDRIK, CHAITANYA; TANG, YI; VARTAK, SHANKUL
To: ELEKTROFI, INC.
Reel/Frame 060910/0245 →
Continuity (6)
Continuation 17351963 · Jun 18, 2021
Continuation PCTUS2020050508 · Sep 11, 2020
Provisional Application 63024703 · May 14, 2020
Provisional Application 62899907 · Sep 13, 2019
Provisional Application 62899981 · Sep 13, 2019
Related Publication 20220389084A1 · Dec 8, 2022
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