IP Library Patent Application 18033730
Patent Application
App. No. 18/033,730

REGIMENS FOR THE TREATMENT OF HAIR LOSS DISORDERS WITH DEUTERATED JAK INHIBITORS

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Quick Facts
Patent No.
US None
App. No.
18/033,730
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 effective amount of Compound (I): or a pharmaceutically acceptable salt thereof.

Claims (23)

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

or a pharmaceutically acceptable salt thereof;

wherein each position designated specifically as deuterium has at least 95% incorporation of deuterium;

wherein the compound, or pharmaceutically acceptable salt thereof, is administered for (1) a first period of 8-24 weeks in an amount in the range of about 8 mg to about 32 mg per day, followed by (2) a second period of at least 8 weeks wherein the compound, or pharmaceutically acceptable salt thereof, is administered in an amount per day that is 50 to 75 percent of the amount per day administered during the first period, such that the hair loss disorder is treated.

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

3 . The method of any one of claims 1 - 2 , wherein, in the first period, the compound, or a pharmaceutically acceptable salt thereof, is administered at about 16 mg/day, about 24 mg/day, or about 32 mg per day.

4 . The method of any one of claims 1 - 3 , wherein, in the second period, the compound, or a pharmaceutically acceptable salt thereof, is administered at about 8 mg/day, about 12 mg/day, or about 16 mg per day.

5 . The method of any one of claims 1 - 4 , wherein in the first period, the compound, or a pharmaceutically acceptable salt thereof, is administered at about 24 mg/day, and in the second period, the compound, or a pharmaceutically acceptable salt thereof, is administered at about 16 mg/day.

6 . The method of claim 5 , wherein the about 24 mg/day of the compound or salt thereof is administered once per day, and the about 16 mg/day is administered once per day.

7 . The method of claim 5 , wherein the about 24 mg/day of the compound or salt thereof is administered as about 12 mg twice per day, and the about 16 mg/day of the compound or salt thereof is administered as about 8 mg twice per day.

8 . The method of any one of claims 1 - 4 , wherein in the first period, the compound, or a pharmaceutically acceptable salt thereof, is administered at about 16 mg/day, and in the second period, the compound, or a pharmaceutically acceptable salt thereof, is administered at about 8 mg/day.

9 . The method of any one of claims 1 - 8 , wherein the compound, or a pharmaceutically acceptable salt thereof, is administered orally.

10 . The method of any one of claims 1 - 9 , wherein the compound, or a pharmaceutically acceptable salt thereof, is administered in a pharmaceutical formulation which is a tablet.

11 . The method of any one of claims 1 - 6 or 8 - 10 , wherein the compound, or a pharmaceutically acceptable salt thereof, is administered once per day in the first period.

12 . The method of any one of claims 1 - 5 or 7 - 10 , wherein the compound, or a pharmaceutically acceptable salt thereof, is administered twice per day in the first period.

13 . The method of any one of claims 1 - 12 , wherein the first period is about 8-12 weeks.

14 . The method of any one of claims 1 - 12 , wherein the first period is about 24 weeks.

15 . The method of any one of claims 1 - 14 , wherein the second period is at least 12 weeks.

16 . The method of any one of claims 1 - 15 , wherein the second period is at least 24 weeks.

17 . The method of any one of claims 1 - 16 , wherein in Compound (I), each position designated specifically as deuterium has at least 97% incorporation of deuterium.

18 . The method of any one of claims 1 - 17 , wherein the subject experiences a ≥50% decrease in SALT score at the end of the first period relative to the subject's baseline SALT score prior to treatment

19 . The method of any one of claims 1 - 18 , wherein the subject's SALT score is less than or equal to 20 at the end of the second period.

20 . The method of any one of claims 1 - 17 , wherein the subject's SALT score is less than or equal to 20 at the end of the first period.

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: CASSELLA, JAMES V.
To: CONCERT PHARMACEUTICALS, INC.
Reel/Frame 063851/0062 →
MERGER Recorded Jun 1, 2023
From: CONCERT PHARMACEUTICALS, INC.
To: SUN PHARMACEUTICALS INDUSTRIES, INC.
Reel/Frame 063818/0961 →