IP Library Granted Patent US 11,040,967
Granted Patent B2
US 11,040,967 · App. 16/417,901 · Granted Jun 22, 2021

TYK2 inhibitors, uses, and methods for production thereof

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Quick Facts
Patent No.
US 11,040,967
App. No.
16/417,901
Filed
May 21, 2019
Granted
Jun 22, 2021
Kind
B2
Art Unit
1626
USPC
514/210.18
Abstract

The present invention provides compounds of formula I useful as inhibitors of Tyrosine Kinase 2 (Tyk2) solid forms and compositions thereof, methods of producing the same, and methods of using the same in the treatment of Tyk2-mediated diseases.

Claims (35)

1. A method for inhibiting non-receptor tyrosine protein kinase 2 (Tyk2) in a patient in need thereof, comprising administering to the patient a compound of Formula I:

or a pharmaceutically acceptable salt thereof,

wherein the patient suffers from a Tyk2-mediated disorder and the Tyk2-mediated disorder is selected from:

a) an autoimmune disorder selected from ankylosing spondylitis, systemic lupus erythematosus, multiple sclerosis, systemic sclerosis, psoriasis, Crohn's disease, and ulcerative colitis;

b) an inflammatory disorder selected from psoriatic arthritis, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, psoriasis, and inflammatory bowel disease;

c) T-cell acute lymphoblastic leukemia (T-ALL);

d) an endocrine disorder selected from polycystic ovary syndrome, Crouzon's syndrome, and type 1 diabetes;

e) Alzheimer's disease; or

f) a disorder associated with transplantation selected from transplant rejection and graft versus host disease;

wherein each of X, Y, and Z is independently hydrogen or deuterium.

2. The method of claim 1 , wherein the disorder is an autoimmune disorder selected from ankylosing spondylitis, systemic lupus erythematosus, multiple sclerosis, systemic sclerosis, psoriasis, Crohn's disease, and ulcerative colitis.

3. The method of claim 1 , wherein the disorder is an inflammatory disorder selected from rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, and inflammatory bowel disease.

4. The method of claim 1 , wherein the disorder is T-cell acute lymphoblastic leukemia (T-ALL).

5. The method of claim 4 , wherein the T-cell acute lymphoblastic leukemia is associated with one or more activating mutations in TYK2.

6. The method of claim 1 , wherein the disorder is a disorder associated with transplantation selected from transplant rejection and graft versus host disease.

7. The method of claim 1 , wherein the disorder is an endocrine disorder selected from polycystic ovary syndrome, Crouzon's syndrome, and type 1 diabetes.

8. The method of claim 1 , wherein the disorder is Alzheimer's disease.

9. A method of treating a Tyk2-mediated disorder comprising administering to a patient in need thereof a compound of Formula I:

or a pharmaceutically acceptable salt thereof,

wherein the patient suffers from a Tyk2-mediated disorder and the Tyk2-mediated disorder is selected from:

a) an autoimmune disorder selected from ankylosing spondylitis, systemic lupus erythematosus, psoriasis, Crohn's disease, and ulcerative colitis; or

b) an inflammatory disorder selected from psoriatic arthritis and inflammatory bowel disease;

wherein each of X, Y, and Z is independently hydrogen or deuterium.

10. The method of claim 9 , wherein the disorder is ankylosing spondylitis.

11. The method of claim 9 , wherein the disorder is systemic lupus erythematosus.

12. The method of claim 9 , wherein the disorder is psoriasis.

13. The method of claim 9 , wherein the disorder is Crohn's disease.

14. The method of claim 9 , wherein the disorder is ulcerative colitis.

15. The method of claim 9 , wherein the disorder is psoriatic arthritis.

16. The method of claim 9 , wherein the disorder is inflammatory bowel disease.

17. A method of treating a Tyk2-mediated disorder comprising administering to a patient in need thereof a compound of Formula I:

or a pharmaceutically acceptable salt thereof,

wherein the Tyk2-mediated disorder is T-cell acute lymphoblastic leukemia (T-ALL);

wherein each of X, Y, and Z is independently hydrogen or deuterium.

18. The method of claim 17 , wherein the T-cell acute lymphoblastic leukemia is associated with one or more activating mutations in TYK2.