IP Library Granted Patent US 12,076,323
Granted Patent B2
US 12,076,323 · App. 16/704,402 · Granted Sep 3, 2024

Treatment of hair loss disorders with deuterated JAK inhibitors

Inventors: Amanda T. Wagner (Watertown, MA); James V. Cassella (Essex, CT); Philip B. Graham (Boston, MA); Virginia Braman (Winchester, MA); Vinita Uttamsingh (Chestnut Hill, MA); Jana Von Hehn (Newton, MA); Colleen E. Hamilton (Carlisle, MA)
Assignee: Sun Pharmaceuticals Industries, Inc.
A61K31/519A61K9/0053A61K9/2009A61K9/2013A61K9/2027A61K9/2054A61P17/14
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 12,076,323
App. No.
16/704,402
Granted
Sep 3, 2024
Kind
B2
Abstract

Disclosed is a method of treating in a subject hair loss disorders that are beneficially treated by administering a JAK1 and/or JAK2 inhibitor. The method comprises administering to the subject an amount in the range of about 4 mg to about 50 mg of Compound (I): or a pharmaceutically acceptable salt thereof. This invention also provides compositions comprising Compound (I) and the use of such compositions in the described methods.

Claims (32)

1. A method of treating a hair loss disorder in a human subject, the method comprising administering to the human subject 16 mg/day of a compound represented by the following structural formula:

or a pharmaceutically acceptable salt thereof, wherein each position in Compound (I) designated specifically as deuterium has at least 95% incorporation of deuterium.

2. The method of claim 1 , wherein the hair loss disorder is alopecia areata.

3. The method of claim 1 , wherein the compound is administered orally.

4. The method of claim 1 , wherein the compound is administered in a pharmaceutical formulation which is a tablet.

5. The method of claim 1 , wherein the compound is administered once a day.

6. The method of claim 1 , wherein the compound is administered twice a day.

7. The method of claim 6 , wherein the step of administering comprises administering to the subject 8 mg of the compound twice per day.

8. The method of claim 1 , wherein the incorporation of deuterium at each position designated specifically as deuterium is at least 97%.

9. The method of claim 1 , wherein the compound is orally administered as a phosphate salt.

10. The method of claim 9 , wherein the phosphate salt is administered once a day.

11. The method of claim 9 , wherein the phosphate salt is administered twice a day.

12. The method of claim 8 , wherein the compound is orally administered as a phosphate salt.

13. The method of claim 12 , wherein the phosphate salt is administered once a day.

14. The method of claim 12 , wherein the phosphate salt is administered twice a day.

15. The method of claim 2 , wherein the compound is administered orally.

16. The method of claim 2 , wherein the compound is administered in a pharmaceutical formulation which is a tablet.

17. The method of claim 2 , wherein the compound is administered once a day.

18. The method of claim 2 , wherein the compound is administered twice a day.

19. The method of claim 18 , wherein the step of administering comprises administering to the subject 8 mg of the compound twice per day.

20. The method of claim 2 , wherein the incorporation of deuterium at each position designated specifically as deuterium is at least 97%.

21. The method of claim 2 , wherein the compound is orally administered as a phosphate salt.

22. The method of claim 21 , wherein the phosphate salt is administered once a day.

23. The method of claim 21 , wherein the phosphate salt is administered twice a day.

24. The method of claim 20 , wherein the compound is orally administered as a phosphate salt.

25. The method of claim 24 , wherein the phosphate salt is administered once a day.

26. The method of claim 24 , wherein the phosphate salt is administered twice a day.

27. A method of treating alopecia areata in a human subject, the method comprising orally administering to the human subject 8 mg twice per day of a compound represented by the following structural formula:

wherein Compound (I) is administered as a phosphate salt, and

wherein each position in Compound (I) designated specifically as deuterium has at least 95% incorporation of deuterium.

28. The method of claim 27 , wherein the incorporation of deuterium at each position designated specifically as deuterium is at least 97%.

29. The method of claim 28 , wherein the Compound (I) is administered in a tablet.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME PREVIOUSLY RECORDED ON REEL 063818 FRAME 0961. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER. Recorded Jul 20, 2023
From: CONCERT PHARMACEUTICALS, INC.
To: SUN PHARMACEUTICAL INDUSTRIES, INC.
Reel/Frame 064352/0539 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 5, 2023
From: WAGNER, AMANDA T.; CASSELLA, JAMES V.; GRAHAM, PHILIP B.; BRAMAN, VIRGINIA; UTTAMSINGH, VINITA; VON HEHN, JANA; HAMILTON, COLLEEN E.
To: CONCERT PHARMACEUTICALS, INC.
Reel/Frame 063850/0895 →
MERGER Recorded Jun 1, 2023
From: CONCERT PHARMACEUTICALS, INC.
To: SUN PHARMACEUTICALS INDUSTRIES, INC.
Reel/Frame 063818/0961 →
Continuity (9)
Continuation 16098338
Provisional Application 62492758 · May 1, 2017
Provisional Application 62466358 · Mar 2, 2017
Provisional Application 62434404 · Dec 14, 2016
Provisional Application 62419237 · Nov 8, 2016
Provisional Application 62418774 · Nov 7, 2016
Provisional Application 62338869 · May 19, 2016
Provisional Application 62331827 · May 4, 2016
Related Publication 20200222408A1 · Jul 16, 2020
Cited By (1)
US 12,364,699