IP Library › Granted Patent US 11,304,949
Granted Patent B2
US 11,304,949 · App. 16/370,436 · Granted Apr 19, 2022

Treatment of hidradenitis suppurativa using JAK inhibitors

Inventors: Michael D. Howell (Kennett Square, PA); Paul Smith (Wilmington, DE)
Assignee: Incyte Corporation
A61K31/519A61K31/573A61K45/06
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Quick Facts
Patent No.
US 11,304,949
App. No.
16/370,436
Granted
Apr 19, 2022
Kind
B2
Abstract

The present application provides methods of treating hidradenitis suppurativa in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound which inhibits JAK1 and/or JAK2, or a pharmaceutically acceptable salt thereof.

Claims (18)

1. A method of treating hidradenitis suppurativa in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound which is:

4[3-(cyanomethyl)-3-(3′,5′-dimethyl-1H,1′H-4,4′-bipyrazol-1-yl)azetidin-1-yl]-2,5-difluoro-N-[(1S)-2,2,2-trifluoro-1-methylethyl]benzamide, or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein the compound or salt is selective for JAK1 over JAK2, JAK3, and TYK2.

3. The method of claim 1 , wherein the compound is a pharmaceutically acceptable salt of 4[3-(cyanomethyl)-3-(3′,5′-dimethyl-1H,1H-4,4′-bipyrazol-1-yl)azetidin-1-yl]-2,5-difluoro-N-[(1S)-2,2,2-trifluoro-1-methylethyl]benzamide.

4. The method of claim 3 , wherein the salt is 4-[3-(cyanomethyl)-3-(3′,5′-dimethyl-1H, 1′H-4,4′-bipyrazol-1-yl)azetidin-1-yl]-2,5-difluoro-N-[(1S)-2,2,2-trifluoro-1-methylethyl]benzamide phosphoric acid salt.

5. The method of claim 1 , wherein the compound or salt is administered at a dosage of 15, 30, 60 or 90 mg on a free base basis.

6. The method of claim 1 , further comprising administering an additional therapeutic agent.

7. The method of claim 6 , wherein the additional therapeutic agent is an antibiotic, a retinoid, a corticosteroid, an anti-TNF-alpha agent, or an immunosuppressant.

8. The method of claim 7 , wherein the antibiotic is clindamycin, doxycycline, minocycline, trimethoprim-sulfamethoxazole, erythromycin, metronidazole, rifampin, moxifloxacin, dapsone, or a combination thereof.

9. The method of claim 7 , wherein the retinoid is etretinate, acitretin, or isotretinoin.

10. The method of claim 7 , wherein the corticosteroid is triamcinolone, dexamethasone, fluocinolone, cortisone, prednisone, prednisolone or flumetholone.

11. The method of claim 7 , wherein the anti-TNF-alpha agent is infliximab, etanercept, or adalimumab.

12. The method of claim 7 , wherein the immunosuppressant is methotrexate, cyclosporin A, mycophenolate mofetil, or mycophenolate sodium.

13. The method of claim 6 , wherein the additional therapeutic agent is finasteride, metformin, adapalene, or azelaic acid.

14. The method of claim 1 , wherein the administrating of the compound or salt is topical.

15. The method of claim 1 , wherein the administering of the compound or salt is oral.

16. The method of claim 1 , wherein the method results in a 10%, 20%, 30%, 40%, or 50% improvement in HiSCR (Hidradenitis Suppurativa Clinical Response).

17. The method of claim 1 , wherein the compound is 4-[3-(cyanomethyl)-3-(3′,5′-dimethyl-1H,1′H-4,4′-bipyrazol-1-yl)azetidin-1-yl]-2,5-difluoro-N-[(1S)-2,2,2-trifluoro-1-methylethyl]benzamide free base.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2019
From: HOWELL, MICHAEL D.; SMITH, PAUL
To: INCYTE CORPORATION
Reel/Frame 049699/0596 →
Continuity (2)
Provisional Application 62650600 · Mar 30, 2018
Related Publication 20190328739A1 · Oct 31, 2019
Cited By (4)
US 12,268,667 US 12,280,054 US 12,336,998 US 12,569,487