IP Library Granted Patent US 10,688,186
Granted Patent B2
US 10,688,186 · App. 15/690,192 · Granted Jun 23, 2020

Anti-CD3 antibody formulations

Inventor: Kunwar Shailubhai (Audubon, PA)
Assignee: Tiziana Life Sciences PLC
A61K47/20A61K9/485A61K9/4858A61K9/4866A61K9/4891A61K39/3955A61K39/39591A61K45/06A61K47/02A61K47/12A61K47/183A61K47/26A61P1/16A61P37/06C07K16/2809A61K2039/505A61K2039/54A61K2039/545C07K2317/565
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Quick Facts
Patent No.
US 10,688,186
App. No.
15/690,192
Granted
Jun 23, 2020
Kind
B2
Abstract

This invention relates to therapeutic, diagnostic and/or prophylactic formulations and dosages and dosing regimens of anti-CD3 antibodies, as well as to methods for using such formulations and dosages and dosing regimens.

Claims (43)

1. A formulation comprising: anti-CD3 antibody comprising a heavy chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 10 and a light chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 11, sodium acetate trihydrate, sodium chloride, polysorbate 80, trehalose, and methionine.

2. The formulation of claim 1 , further comprising EDTA.

3. The formulation of claim 1 , wherein the formulation is a liquid.

4. The formulation of claim 1 , wherein the formulation is a lyophilized powder.

5. The formulation of claim 1 , comprising a unit dose of the anti-CD3 antibody.

6. The formulation of claim 5 , wherein the unit dose is about 0.1 mg to 10 mg.

7. The formulation of claim 6 , wherein the unit dose is 0.5 mg, 2.5 mg or 5.0 mg.

8. The formulation of claim 3 , wherein the concentration of:

a. sodium acetate trihydrate is about 10 mM to 500 mM;

b. sodium chloride is about 10 mM to 500 mM;

c. polysorbate 80 is about 0.01% to 1% (w/v);

d. trehalose is about 5% to 50% (w/v); and

e. methionine is 0.01% to 1% (w/v).

9. The formulation of claim 8 , where the concentration of EDTA is about 0.01% to 1% (w/v).

10. The formulation of claim 8 , wherein the solution is at a pH in the range of 4 to 6.

11. A lyophilized powder of the formulation of claim 8 .

12. A liquid formulation comprising a unit dose of about 0.1 mg to 10 mg of an anti-CD3 antibody comprising a heavy chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 10 and a light chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 11, 25 mM sodium acetate trihydrate, 125 mM sodium chloride, 0.02% polysorbate 80 (w/v), 20% trehalose (w/v), and 0.1% methionine(w/v).

13. The formulation of claim 11 , further comprising 0.1% EDTA (w/v).

14. The liquid formulation of claim 12 , wherein the unit dose is 0.5 mg, 2.5 mg or 5.0 mg.

15. A lyophilized powder of the formulation of claim 12 .

16. The formulation of claim 4 , wherein the ratio of anti-CD3 antibody to:

a. polysorbate 80 is about 1:0.01 to 0.1 (w/w);

b. trehalose is about 1:10 to 50 (w/w);

c. methionine about 1:0.1 to 0.5 (w/w);

d. sodium acetate trihydrate is about 1:0.1 to 1.0 (w/w); and

e. sodium chloride is about 1:0.5 to 2.0 (w/w).

17. The formulation of claim 16 , where the ratio of anti-CD3 antibody to EDTA is about 1: 0.1 to 0.5 (w/w).

18. A powder formulation comprising a unit dose of about 0.1 mg to 10 mg of an anti-CD3 antibody comprising a heavy chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 10 and a light chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 11 and about 0.58 mg of sodium acetate trihydrate, 1.25 mg sodium chloride, 0.034 mg polysorbate 80, 34 mg trehalose and 0.17 mg methionine per 1 mg of anti-CD3 antibody.

19. The powder formulation of claim 18 , further comprising 0.17 mg EDTA per 1 mg of anti-CD3 antibody comprising a heavy chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 10 and a light chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 11.

20. The powder formulation of claim 18 , wherein the unit dose is 0.5 mg, 2.5 mg or 5.0 mg.

21. An enteric coated oral capsule comprising the formulation of claim 18 .

22. An enteric coated oral capsule containing an anti-CD3 antibody lyophilized formulation comprising a unit dose of about 0.1 mg to 10 mg of an anti-CD3 antibody comprising a heavy chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 10 and a light chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 11 and about 0.58 mg of sodium acetate trihydrate, 1.25 mg sodium chloride, 0.034 mg polysorbate 80, 34 mg trehalose and 0.17 mg methionine per 1 mg of anti-CD3 antibody.

23. The enteric-coated oral capsule of claim 22 , wherein the anti-CD3 antibody lyophilized formulation further comprises 0.17 mg EDTA per 1 mg of anti-CD3 antibody.

24. The enteric-coated oral capsule of claim 22 , wherein the unit dose is 0.5 mg, 2.5 mg or 5.0 mg.

25. An enteric coated oral capsule containing an anti-CD3 antibody liquid formulation comprising a unit dose of about 0.1 mg to 10 mg of an anti-CD3 antibody comprising a heavy chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 10 and a light chain amino acid sequence comprising the amino acid sequence of SEQ ID NO: 11, 25 mM sodium acetate trihydrate, 125 mM sodium chloride, 0.02% polysorbate 80 (w/v), 20% trehalose (w/v), and 0.1% methionine(w/v).

26. The enteric-coated oral capsule of claim 25 , anti-CD3 antibody liquid formulation further comprises 0.1% EDTA.

27. The enteric-coated oral capsule of claim 25 , wherein the unit dose is 0.5 mg, 2.5 mg or 5.0 mg.

28. The formulation of claim 1 , wherein the formulation further comprises as least one additional active agent selected from the group consisting of: an NF-κB inhibitor, a GLP-1 or a beta cell resting compound, mesalamine or another 5-ASA drug, pentoxifylline, ursodeoxycholic acid, a PPARγ agonist, All Trans Retinoic Acid (ATRA), DPP-4 (gliptins-sitagliptin), a fatty acid synthesis inhibitor, a FXR agonist), fexaramine, cafestol, bile Acid Sequestrants, SGLT2 inhibitors, an anti-IL-6R mAb, an anti-TNF antibody, Etanercept, anti-inflammatory and/or immunosuppressive compounds, tacrolimus, corticosteroids, statins, interferon beta, glatiramer acetate, interferon beta-1a, interferon beta-1b, mitoxantrone, dexamethasone, methylprednisolone, prednisone, and an anti-obesity drug.

29. An enteric coated oral capsule of claim 25 containing an antibody liquid formulation comprising a unit dose of an antibody, 20% trehalose (w/v), and 0.1% methionine(w/v).

30. An enteric coated oral capsule of claim 25 containing an antibody lyophilized formulation comprising a unit dose an antibody and about 34 mg trehalose and 0.17 mg methionine per mg of antibody.

31. The enteric coated oral capsule of claim 25 , wherein the antibody has an IgG1 isotype.

32. The formulation of claim 1 , further comprising mannitol.

33. The formulation of claim 1 , wherein the formulation is an oral formulation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2018
From: SHAILUBHAI, KUNWAR
To: TIZIANA LIFE SCIENCES PLC
Reel/Frame 045131/0759 →
Continuity (2)
Provisional Application 62380652 · Aug 29, 2016
Related Publication 20180177880A1 · Jun 28, 2018
Cited By (1)
US 12,565,529