IP Library Granted Patent US 11,324,736
Granted Patent B2
US 11,324,736 · App. 16/946,402 · Granted May 10, 2022

Method of Treating Focal Segmental Glomerulosclerosis

Inventors: Zhenhua Miao (Mountain View, CA); Thomas Schall (Mountain View, CA); Rajinder Singh (Mountain View, CA)
Assignee: ChemoCentryx, Inc.
A61K31/444A61K31/137A61K31/28A61K31/403A61K31/4178A61K31/4184A61K31/426A61K31/44A61K31/4418A61K31/4422A61K31/519A61K31/7034A61K35/545A61K39/3955A61P13/12
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Quick Facts
Patent No.
US 11,324,736
App. No.
16/946,402
Granted
May 10, 2022
Kind
B2
Abstract

A method of treating focal segmental glomerulosclerosis with a compound of Formula I is provided. FSGS may be primary (no known cause) or secondary. The secondary FSGS may be associated with infections or viruses such as HIV, diseases such as sickle cell disease or lupus, toxins or drugs such as anabolic steroids, heroin or pamidronate, nephron loss and hyperfiltration, such as with chronic pyelonephritis and reflux, morbid obesity, or diabetes mellitus.

Claims (39)

1. A method of treating nephritis, wherein the nephritis is lupus nephritis, IgA nephropathy, or immune-checkpoint therapy-related interstitial nephritis in a patient in need thereof, comprising administering to the patient an effective amount of a compound of Formula I:

or a pharmaceutically acceptable salt thereof, wherein

R 1 is halogen or C 1-6 alkyl;

R 2 is hydrogen, halogen, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 1-6 haloalkoxy, or —CN;

R 3 is hydrogen, halogen, or C 1-6 alkyl;

R 4 is hydrogen, halogen, or C 1-6 alkyl;

each R 5 is independently C 1-6 alkyl, —OH, or —NH 2 ;

n is 0, 1, 2, or 3; and

each of A 1 , A 2 , and A 3 is —CH— or —N—, where at least one of A 1 , A 2 , or A 3 is —N—.

2. The method of claim 1 wherein R 1 is halogen or methyl;

R 2 is halogen or C 1-3 haloalkyl;

R 3 is halogen or C 1-3 alkyl;

R 4 is hydrogen;

n is 0;

A 2 is —CH—; and A 3 is —N—.

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

or a pharmaceutically acceptable salt thereof.

4. The method of claim 1 , wherein the compound is

or a pharmaceutically acceptable salt thereof.

5. The method of claim 1 , wherein the compound is

or a pharmaceutically acceptable salt thereof.

6. The method of claim 1 , wherein the compound or a pharmaceutically acceptable salt thereof is administered orally.

7. The method of claim 1 , wherein the compound or a pharmaceutically acceptable salt thereof is administered twice per day.

8. The method of claim 1 , wherein the compound or a pharmaceutically acceptable salt thereof is administered once per day.

9. The method of claim 1 , further comprising administering to the patient one or more additional therapeutic compound.

10. The method of claim 9 wherein the one or more additional therapeutic compound is selected from one or more of an antihypertensive, a statin, a vasodilator, a steroid, a cytotoxic drug, a diuretic, a non-steriodal anti-inflammatory drug (NSAID), a cholesterol or triglycerides reducing agent, and an immunosuppressive drug.

11. The method of claim 9 wherein the one or more additional therapeutic compound is selected from the group consisting of an angiotensin converting enzyme (ACE) inhibitor and an angiotensin receptor II blocker (ARB).

12. The method of claim 11 wherein the one or more additional therapeutic compound is selected from the group consisting of ramipril, perindopril, lisinopril, perindopril arginine, captopril, spirapril, quinapril, enalapril, imidapril, fosinopril, zofenopril, benazepril, trandolapril, verapamil, benazepril, amlodipine, trandolapril, P-003, cilazapril, delapril, moexipril, quinapril, fosinopril, temocapril, losartan, candesartan, irbesartan, telmisartan, olmesartan, valsartan, azilsartan, telmisartan, fimasartan, EMA-401, azilsartan medoxomil potassium, sparsentan, candesartan cilexetil, olmesartan medoxomil, TRV-027, losartan potassium, YH-22189, azilsartan trimethylethanolamine, allisartan isoproxil, and eprosartan.

13. The method of claim 1 , wherein the patient is also subjected to extracorporeal blood purification, allogenic transplantation, and/or stem cell therapy.

14. The method of claim 9 , wherein the one or more additional therapeutic compound is administered concurrently or sequentially.

15. The method of claim 9 , wherein the one or more additional therapeutic compound is administered as a single pharmaceutical composition together with the compound of formula I or as a separate pharmaceutical composition.

16. The method of claim 1 , wherein the effective amount of the compound of Formula I is 5 mg administered twice daily.

17. The method of claim 1 , wherein the effective amount of the compound of Formula I is 10 mg administered twice daily.

18. The method of claim 1 , wherein the effective amount of the compound of Formula I is 15 mg administered twice daily.

19. The method of claim 1 , wherein the effective amount of the compound of Formula I is 10 mg administered once daily.

20. The method of claim 1 , wherein the effective amount of the compound of Formula I is 15 mg administered once daily.

21. The method of claim 1 , wherein the nephritis is lupus nephritis.

22. The method of claim 1 , wherein the nephritis is IgA nephropathy.

23. The method of claim 1 , wherein the nephritis is immune-checkpoint therapy-related interstitial nephritis.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2022
From: MIAO, ZHENHUA; SCHALL, THOMAS; SINGH, RAJINDER
To: CHEMOCENTRYX, INC.
Reel/Frame 058617/0172 →
Continuity (3)
Continuation 15821490 · Nov 22, 2017
Provisional Application 62425832 · Nov 23, 2016
Related Publication 20200323832A1 · Oct 15, 2020
Cited By (1)
US 12,194,032