IP Library Granted Patent US 10,980,884
Granted Patent B2
US 10,980,884 · App. 16/441,092 · Granted Apr 20, 2021

Stable aqueous etanercept composition

Inventors: Mark Manning (Johnstown, CO); Brian Murphy (Fort Collins, CO)
Assignee: Coherus Biosciences, Inc.
A61K47/26A61K9/0019A61K9/08A61K9/14A61K9/16A61K38/17A61K38/1793A61K38/191A61K39/39591A61K47/10A61K47/18C07K14/705C07K14/7151A61P17/06A61P19/02A61P29/00C07K2319/30
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Quick Facts
Patent No.
US 10,980,884
App. No.
16/441,092
Granted
Apr 20, 2021
Kind
B2
Abstract

The invention provides stabilized aqueous pharmaceutical etanercept compositions suitable for long-term storage of etanercept, methods of manufacture of these compositions, methods of administration, and kits containing same.

Claims (26)

1. A stable aqueous pharmaceutical composition comprising:

an aqueous carrier;

about 50 mg/mL etanercept, about 1% (w/v) sucrose, 0.26% (w/v) to 2% (w/v) mannitol or lysine; the aqueous carrier comprises a citrate buffer, the composition is free of arginine and cysteine, the composition has a pH of about 6.0 to about 6.6, the composition has at least 90 wt. % correctly folded etanercept, the composition has less than 1 wt. % aggregates of etanercept, and

has at M 3 or T 2 or T 4 no more than, on average, about 10,000 subvisible particles per mL having a size greater than 5 μm,

and the combination of said sucrose and said mannitol or lysine stabilizes said etanercept in said stable aqueous pharmaceutical composition, and

wherein said stable aqueous pharmaceutical composition contains less than 50 mM NaCl,

wherein the composition has an osmolality from about 180 to about 420 mOsM, and wherein the etanercept is prepared by a mixed mode cation exchange chromatography and mixed mode anion exchange chromatography method resulting in less than 1 wt. % aggregates of etanercept.

2. The stable aqueous pharmaceutical composition of claim 1 , comprising about 25 mM NaCl.

3. The stable aqueous pharmaceutical composition of claim 1 , eliciting long term storage stability as characterized by at least one of:

SEC analysis at M 3 or T 4 at 40° C. of: monomer content greater than 90 wt. %;

aggregate content of less than 1 wt. %; and fragment 3 content less than 5 wt %; and HIC analysis at M 3 or T 2 or T 4 wherein the amount of the composition represented by peak 1 of the HIC chromatogram is less than about 3 wt. %.

4. The stable aqueous pharmaceutical composition of claim 1 , wherein the composition is characterized by SEC analysis at M 3 or T 2 or T 4 in which fragment 3 content is less than about 10 wt. %.

5. The stable aqueous pharmaceutical composition of claim 1 , eliciting long term storage stability as characterized by: an HIC analysis at M 3 or T 2 or T 4 wherein the amount of the composition represented by peak 2 of the HIC chromatogram is greater than or equal to about 95 wt. %; and wherein, if peak 3 is present on the HIC chromatogram, the amount of the composition represented by peak 3 is less than or equal to about 3 wt. %.

6. The stable aqueous pharmaceutical composition of claim 1 , further comprising a buffer selected from the group consisting of phosphate, maleate, tartrate, succinate, acetate, tris (hydroxymethyl)-aminoethane (tris), bicarbonate, or a combination thereof.

7. The stable aqueous pharmaceutical composition of claim 1 , further comprising a tonicity modifier selected from the group consisting of potassium chloride, sodium citrate or combinations thereof and about 25 mM NaCl, and a buffer selected from the group consisting of phosphate, histidine, maleate, tartrate, succinate, acetate, tris-(hydroxymethyl)-aminomethane (tris), bicarbonate, or a combination thereof.

8. The stable aqueous pharmaceutical composition of claim 1 , comprising a tonicity modifier selected from the group consisting of potassium chloride, sodium citrate or a combination thereof, and about 25 mM NaCl.

9. The stable aqueous pharmaceutical composition of claim 1 , comprising about 10 mM to about 200 mM of a tonicity modifier selected from the group consisting of potassium chloride, sodium citrate or a combination thereof, and about 25 mM NaCl.

10. A vial, syringe, or injector pen containing the stable aqueous pharmaceutical composition of claim 1 .

11. The vial, syringe, or injector pen of claim 10 , comprising about 10 mM to about 200 mM of a tonicity modifier selected from the group consisting of potassium chloride, sodium citrate or a combination thereof, and about 25 mM NaCl.

12. A method of treating a patient in need of treatment with etanercept, comprising administering a therapeutically effective amount of the stable aqueous pharmaceutical composition of claim 1 to said patient.

13. The stable aqueous pharmaceutical composition of claim 1 , wherein the etanercept is 50 mg/mL.

14. The stable pharmaceutical composition of claim 1 , wherein the sucrose is 1% (w/v).

15. The vial, syringe or injection pen of claim 10 , wherein the etanercept is 50 mg/mL.

16. The vial, syringe or injection pen of claim 10 , wherein the sucrose is 1% (w/v).

17. The method of claim 12 , wherein the etanercept is 50 mg/mL.

18. The method of claim 12 , wherein the sucrose is 1% (w/v).

Assignments (3)
TERMINATION AND RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY AT REEL/FRAME NO. 59436/0055 Recorded May 9, 2024
From: BIOPHARMA CREDIT PLC, AS COLLATERAL AGENT
To: COHERUS BIOSCIENCES, INC.; COHERUS INTERMEDIATE CORP.; INTEKRIN THERAPEUTICS INC.
Reel/Frame 067378/0256 →
SECURITY INTEREST Recorded May 8, 2024
From: COHERUS BIOSCIENCES, INC.; COHERUS INTERMEDIATE CORP.; INTEKRIN THERAPEUTICS INC.; SURFACE ONCOLOGY, LLC; COHERUS ONCOLOGY SUPPORTIVE CARE LLC
To: ANKURA TRUST COMPANY, LLC
Reel/Frame 067348/0160 →
SECURITY INTEREST Recorded Mar 18, 2022
From: COHERUS BIOSCIENCES, INC.; COHERUS INTERMEDIATE CORP.; INTEKRIN THERAPEUTICS INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 059436/0055 →
Continuity (6)
Continuation 15917333 · Mar 9, 2018
Continuation 15078755 · Mar 23, 2016
Continuation 13654950 · Oct 18, 2012
Provisional Application 61669480 · Jul 9, 2012
Provisional Application 61548518 · Oct 18, 2011
Related Publication 20190290766A1 · Sep 26, 2019