IP Library Granted Patent US 11,806,399
Granted Patent B2
US 11,806,399 · App. 17/175,162 · Granted Nov 7, 2023

Excipient compounds for biopolymer formulations

Inventors: David S. Soane (Palm Beach, FL); Philip Wuthrich (Watertown, MA); Rosa Casado Portilla (Middleton, MA); Robert P. Mahoney (Newbury, MA); Mark Moody (Concord, MA); Daniel G. Greene (Reading, MA)
Assignee: COMERA LIFE SCIENCES, INC.
A61K39/39591A61K38/1793A61K38/1816A61K38/193A61K47/02A61K47/12A61K47/18A61K47/20A61K47/22A61K47/42A61K47/60C07K16/22C07K16/241C07K16/32C12N9/2462C12N9/96C12Y302/01017
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,806,399
App. No.
17/175,162
Granted
Nov 7, 2023
Kind
B2
Abstract

The invention encompasses formulations and methods for the production thereof that permit the delivery of concentrated protein solutions. The inventive methods can yield a lower viscosity liquid protein formulation or a higher concentration of therapeutic or nontherapeutic proteins in the liquid formulation, as compared to traditional protein solutions. The inventive methods can also yield a higher stability of a liquid protein formulation.

Claims (32)

1. An injectable liquid pharmaceutical formulation comprising:

a) at least about 10 mg/ml therapeutic antibody;

b) a viscosity reducing amount of caffeine, wherein the viscosity reducing amount of caffeine is 2% or less by weight of the injectable liquid pharmaceutical formulation; and

c) a viscosity reducing amount of an aromatic acid,

wherein viscosity of the injectable liquid pharmaceutical formulation is less than about 100 cP.

2. The injectable liquid pharmaceutical formulation of claim 1 , wherein the aromatic acid is salicylic acid.

3. The injectable liquid pharmaceutical formulation of claim 1 , wherein the aromatic acid is nicotinic acid.

4. The injectable liquid pharmaceutical formulation of claim 3 , wherein the aromatic acid is nicotinic acid sodium salt.

5. The injectable liquid pharmaceutical formulation of claim 1 , wherein the viscosity reducing amount of caffeine is less than about 20 mg/ml.

6. The injectable liquid pharmaceutical formulation of claim 1 , wherein the injectable liquid pharmaceutical formulation further comprises a buffer.

7. The injectable liquid pharmaceutical formulation of claim 6 , wherein the buffer is a histidine buffer.

8. The injectable liquid pharmaceutical formulation of claim 6 , wherein the buffer is a phosphate buffer.

9. The injectable liquid pharmaceutical formulation of claim 1 , wherein the therapeutic antibody is selected from the group consisting of bevacizumab, trastuzumab, adalimumab, infliximab, etanercept, darbepoetin alfa, epoetin alfa, cetuximab, pegfilgrastim, filgrastim, and rituximab.

10. The injectable liquid pharmaceutical formulation of claim 1 , wherein the viscosity of the injectable liquid pharmaceutical formulation is less than about 50 cP.

11. The injectable liquid pharmaceutical formulation of claim 1 , wherein the injectable liquid pharmaceutical formulation contains at least about 100 mg/mL of the therapeutic antibody.

12. The injectable liquid pharmaceutical formulation of claim 1 , wherein the injectable liquid pharmaceutical formulation contains at least about 200 mg/mL of the therapeutic antibody.

13. An injectable liquid pharmaceutical formulation comprising:

a) at least about 10 mg/ml therapeutic antibody; and

b) a viscosity reducing amount of nicotinic acid,

wherein viscosity of the injectable liquid pharmaceutical formulation is less than about 100 cP and the viscosity reducing amount of nicotinic acid is at least 8% by weight of the injectable liquid pharmaceutical formulation.

14. The injectable liquid pharmaceutical formulation of claim 13 , wherein the nicotinic acid is nicotinic acid sodium salt.

15. The injectable liquid pharmaceutical formulation of claim 13 , wherein the injectable liquid pharmaceutical formulation further comprises a hindered amine.

16. The injectable liquid pharmaceutical formulation of claim 13 , wherein the injectable liquid pharmaceutical formulation further comprises a buffer.

17. The injectable liquid pharmaceutical formulation of claim 16 , wherein the buffer is a histidine buffer.

18. The injectable liquid pharmaceutical formulation of claim 16 , wherein the buffer is a phosphate buffer.

19. The injectable liquid pharmaceutical formulation of claim 13 , wherein the therapeutic antibody is selected from the group consisting of bevacizumab, trastuzumab, adalimumab, infliximab, etanercept, darbepoetin alfa, epoetin alfa, cetuximab, pegfilgrastim, filgrastim, and rituximab.

20. The injectable liquid pharmaceutical formulation of claim 13 , wherein the viscosity of the injectable liquid pharmaceutical formulation is less than about 50 cP.

21. The injectable liquid pharmaceutical formulation of claim 13 , wherein the injectable liquid pharmaceutical formulation contains at least about 100 mg/mL of the therapeutic antibody.

22. The injectable liquid pharmaceutical formulation of claim 13 , wherein the injectable liquid pharmaceutical formulation contains at least about 200 mg/mL of the therapeutic antibody.

23. The injectable liquid pharmaceutical formulation of claim 1 , wherein the therapeutic antibody is gamma globulin.

24. The injectable liquid pharmaceutical formulation of claim 1 , wherein the viscosity reducing amount of caffeine is about 15 mg/ml or less.

25. The injectable liquid pharmaceutical formulation of claim 13 , wherein the viscosity reducing amount of nicotinic acid is less than 300 mg/ml.

Assignments (1)
CHANGE OF NAME Recorded Feb 16, 2022
From: REFORM BIOLOGICS, INC.
To: COMERA LIFE SCIENCES, INC.
Reel/Frame 059327/0985 →
Continuity (9)
Continuation 16659046 · Oct 21, 2019
Continuation 15331197 · Oct 21, 2016
Continuation In Part 14966549 · Dec 11, 2015
Continuation 14744847 · Jun 19, 2015
Provisional Application 62014784 · Jun 20, 2014
Provisional Application 62083623 · Nov 24, 2014
Provisional Application 62136763 · Mar 23, 2015
Provisional Application 62245513 · Oct 23, 2015
Related Publication 20210162046A1 · Jun 3, 2021