Compounds and methods of treating or ameliorating an IL-1R-mediated disease or disorder using same

Patent metadata

Field	Value
Publication number	US-10428059-B2
Application number	US-201715726911-A
Country	US
Kind code	B2
Filing date	Oct 6, 2017
Priority date	Aug 4, 2014
Publication date	Oct 1, 2019
Grant date	Oct 1, 2019

Abstract

The present invention provides compounds useful for treating or preventing an IL-1R-mediated disease or disorder. In certain embodiments, the disease or disorder comprises scleroderma.

First claim

What is claimed is:

1. A method of relieving or improving an IL-1R-mediated disease or disorder in a mammal, wherein the IL-1R-mediated disease or disorder is scleroderma or systemic lupus erythematosus (lupus), the method comprising administering to the mammal a therapeutically effective amount of at least one compound, or a salt, tautomer or solvate thereof, wherein the at least one compound is a compound of formula (XI):

wherein in (XI):
each occurrence of R 1 is independently selected from the group consisting of H and methyl;
R 2 is O or —NH; and
R 3 is optionally substituted phenyl or naphthyl.

2. The method of claim 1 , wherein the compound is selected from the group consisting of 1,3-dimethyl-5-(naphthalen-1-yl)-5,11-dihydro-1H-indeno[2′,1′:5,6]pyrido[2,3-d]pyrimidine-2,4,6(3H)-trione; and 2-amino-5-(naphthalen-1-yl)-5,11-dihydro-1H-indeno[2′,1′:5,6]pyrido[2,3-d]pyrimidine-4,6-dione; or a salt, tautomer or solvate thereof.

3. The method of claim 1 , wherein the mammal is further administered at least one therapeutic agent.

4. The method of claim 3 , wherein the therapeutic agent comprises at least one selected from the group consisting of anakinra, rilonacept, azathioprine, methotrexate, bosentan, etanercept, halofuginone, iloprost, cyclophosphamide, cyclosporin A, mycophenolate mofetil, intravenous immunoglobulin, pirfenidone, prednisone, rituximab, beta-glycan peptides, basiliximab, sirolimus, alefacept, terguride, pomalidomide, and a tyrosine kinase inhibitor.

5. The method of claim 3 , wherein the compound and the therapeutic agent are co-administered to the mammal.

6. The method of claim 3 , wherein the compound is administered to the mammal in a given period of time before or after the therapeutic agent is administered to the mammal.

7. The method of claim 1 , wherein the compound is formulated as a pharmaceutical composition.

8. The method of claim 1 , wherein the mammal is human.

Assignees

• Univ Drexel

Inventors

• Kortagere Sandhya
• Artlett Carol M

Classifications

• A61P37/06

  Immunosuppressants, e.g. drugs for graft rejection · CPC title

• A61P37/02

  Immunomodulators · CPC title

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• A61P3/10

  for hyperglycaemia, e.g. antidiabetics · CPC title

• A61P35/02

  specific for leukemia · CPC title