IP Library Granted Patent US 11,534,490
Granted Patent B2
US 11,534,490 · App. 16/720,351 · Granted Dec 27, 2022

Methods of treating psoriasis using IL-17 antagonists

Inventors: Achim Guettner (Binzen, DE); Matthias Machacek (Allschwil, CH); Charis Papavassilis (Loerrach, DE); Oliver Sander (Basel, CH)
Assignee: NOVARTIS AG
A61K39/3955C07K16/244A61K2039/505A61K2039/545C07K2317/34C07K2317/76
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 11,534,490
App. No.
16/720,351
Granted
Dec 27, 2022
Kind
B2
Abstract

The disclosure relates to novel regimens for treating psoriasis, which employ a therapeutically effective amount of an IL-17 antagonist, e.g., an IL-17 binding molecule, e.g., an IL-17 antibody, such as the secukinumab antibody, or an IL-17 receptor binding molecule, e.g., an IL-17 receptor antibody.

Claims (40)

1. A method of treating psoriasis, comprising subcutaneously administering to a patient in need thereof a dose of about 150 mg-about 300 mg of an IL-17 antibody weekly during week 0, 1, 2, 3, and 4, and then bimonthly (twice a month) thereafter, wherein the IL-17 antibody comprises:

i) an immunoglobulin heavy chain variable (VH) domain comprising the amino acid sequence set forth as SEQ ID NO:8, and an immunoglobulin light chain variable (VL) domain comprising the amino acid sequence set forth as SEQ ID NO:10;

ii) an immunoglobulin VH domain comprising the hypervariable regions comprising the amino acid sequences set forth as SEQ ID NO:1, SEQ ID NO:2, and SEQ ID NO:3, respectively; and an immunoglobulin VL domain comprising the hypervariable regions comprising the amino acid sequences set forth as SEQ ID NO:4, SEQ ID NO:5 and SEQ ID NO:6, respectively; or

iii) an immunoglobulin VH domain comprising the hypervariable regions comprising the amino acid sequences set forth as SEQ ID NO:11, SEQ ID NO:12 and SEQ ID NO:13, respectively; and an immunoglobulin VL domain comprising the hypervariable regions comprising the amino acid sequences set forth as SEQ ID NO:4, SEQ ID NO:5 and SEQ ID NO:6, respectively.

2. The method of claim 1 , wherein the dose of the IL-17 antibody is about 150 mg or about 300 mg.

3. The method of claim 2 , wherein the dose of the IL-17 antibody is about 150 mg.

4. The method of claim 2 , wherein the dose of the IL-17 antibody is about 300 mg.

5. The method of claim 2 , wherein the patient has plaque psoriasis.

6. The method of claim 5 , wherein the patient has moderate to severe plaque psoriasis.

7. The method of claim 6 , wherein the patient is an adult patient.

8. The method according to claim 6 , wherein, prior to treatment with the IL-17 antibody, the patient has an Investigator Global Assessment (IGA) score of >3.

9. The method of claim 2 , wherein the patient has palm psoriasis, sole psoriasis, face psoriasis, scalp psoriasis, genital psoriasis, or nail psoriasis.

10. The method according to claim 2 , wherein, prior to treatment with the IL-17 antibody, the patient has not been previously treated with a systemic agent for psoriasis.

11. The method according to claim 2 , wherein, prior to treatment with the IL-17 antibody, the patient has been previously treated with a systemic agent for psoriasis.

12. The method according to claim 11 , wherein the systemic agent is selected from the group consisting of methotrexate, cyclosporine, fumaric acid esters, acitretin, alefacept, adalimumab, efalizumab, etanercept, infliximab, golimumab and ustekinumab.

13. The method according to claim 12 , wherein the systemic agent is methotrexate.

14. The method of claim 2 , wherein the IL-17 antibody has a T max of about 4-3 days.

15. The method of claim 2 , wherein the IL-17 antibody has an absolute bioavailablilty of about 60-about 80%.

16. The method of claim 2 , wherein the IL-17 antibody is a human monoclonal antibody.

17. The method of claim 16 , wherein the IL-17 antibody is of the IgG1/kappa isotype.

18. The method of claim 2 , wherein the dose of the IL-17 antibody is about 300 mg and the patient weighs more than 90 kg.

19. The method of claim 18 , wherein the IL-17 antibody is secukinumab.

20. The method of claim 2 , wherein the dose of the IL-17 antibody is about 300 mg and the patient weighs more than or equal to 90 kg.

21. The method of claim 20 , wherein the IL-17 antibody is secukinumab.

22. The method of claim 2 , wherein the dose of the IL-17 antibody is about 300 mg and the patient weighs more than 100 kg.

23. The method of claim 22 , wherein the IL-17 antibody is secukinumab.

24. The method of claim 2 , wherein the dose of the IL-17 antibody is about 150 mg and the patient weighs less than 90 kg.

25. The method of claim 2 , wherein the dose of the IL-17 antibody is about 150 mg and the patient weighs less than or equal to 90 kg.

26. The method of claim 2 , wherein the dose of the IL-17 antibody is about 150 mg and the patient weighs less than or equal to 100 kg.

27. The method of claim 2 , wherein the IL-17 antibody is comprised in a pharmaceutical formulation, wherein said pharmaceutical formulation further comprises a buffer and a stabilizer.

28. The method of claim 27 , wherein the pharmaceutical formulation is in liquid form.

29. The method of claim 27 , wherein the pharmaceutical formulation is a lyophilisate for reconstitution with an aqueous carrier prior to administration to the patient.

30. The method of claim 27 , wherein the pharmaceutical formulation is contained within at least one pre-filled syringe, at least one vial, at least one injection pen, or at least one autoinjector.

31. The method of claim 27 , wherein the dose of the IL-17 antibody is about 150 mg, wherein the pharmaceutical formulation is contained within a pre-filled syringe, an injection pen, or an autoinjector, which is contained within a kit, and wherein said kit further comprises instructions for use.

32. The method of claim 27 , wherein the dose of the IL-17 antibody is about 300 mg, wherein the pharmaceutical formulation is contained within an autoinjector, wherein said autoinjector is contained within a kit, and wherein said kit further comprises instructions for use.

33. The method of claim 27 , wherein the IL-17 antibody is secukinumab.

34. A method of treating psoriasis, comprising subcutaneously administering to a patient in need thereof a dose of about 150 mg or about 300 mg secukinumab during week 0, 1, 2, 3, and 4, followed by a dose of about 150 mg or about 300 mg secukinumab during a maintenance regimen, wherein the maintenance regimen comprises administering secukinumab to the patient every four weeks if the patient is a responder to treatment with secukinumab or bimonthly (twice a month) if the patient is a partial responder or a non-responder to treatment with secukinumab.

35. The method of claim 34 , wherein the patient weighs more than or equal to 90 kg.

36. A method of treating psoriasis, comprising subcutaneously administering to a patient in need thereof a dose of about 150 mg or 300 mg secukinumab during week 0, 1, 2, 3, and 4, and then bimonthly (twice a month) thereafter.

37. The method of claim 36 , wherein the patient weighs more than or equal to 90 kg.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2026
From: NOVARTIS AG
To: NOVARTIS PHARMA AG
Reel/Frame 075712/0291 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2020
From: GUETTNER, ACHIM; MACHACEK, MATTHIAS; PAPAVASSILIS, CHARIS; SANDER, OLIVER
To: NOVARTIS AG
Reel/Frame 052360/0914 →
Continuity (4)
Continuation 15630577 · Jun 22, 2017
Continuation 13876367
Provisional Application 61391388 · Oct 8, 2010
Related Publication 20200171147A1 · Jun 4, 2020