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

Patent metadata

Field	Value
Publication number	US-11345696-B2
Application number	US-201916537897-A
Country	US
Kind code	B2
Filing date	Aug 12, 2019
Priority date	Aug 4, 2014
Publication date	May 31, 2022
Grant date	May 31, 2022

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 at least one symptom of an IL-1R-mediated disease or disorder in a mammal in need thereof, the method comprising administering to the mammal a therapeutically effective amount of a compound having the structure:
6-amino-4-(2-hydroxynaphthalen-1-yl)-3-methyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile:

or a salt, tautomer, or solvate thereof.

2. The method of claim 1 , wherein the disease or disorder is selected from the group consisting of infectious, inflammatory, and autoimmune.

3. The method of claim 1 , wherein the disease or disorder is selected from the group consisting of scleroderma, inflammation in general, systemic lupus erythematosus (lupus), Sjogren's syndrome, arthritis, myositis, Behcet's disease, inflammatory bowel disease, colitis, septic shock, chronic myelogenous leukemia, acute myelogenous leukemia, multiple myeloma, non-blood cancers, psoriasis, type I and type II diabetes, asbestosis, idiopathic pulmonary fibrosis, graft-versus-host disease, familial Mediterranean fever, stroke, epilepsy, and cryopyrin-associated periodic syndromes (CAPS).

4. The method of claim 3 , wherein the disease or disorder is a non-blood cancer, and wherein the non-blood cancer is at least one selected from the group consisting of glioma, metastatic breast cancer, interleukin-1-producing cancer, pancreatic ductal adenocarcinoma, colorectal, melanoma, gastric carcinoma, cervical cancer, lung carcinoma, and ovarian carcinoma.

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

6. The method of claim 5 , wherein the at least one additional 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.

7. The method of claim 5 , wherein the compound and the at least one additional therapeutic agent are co-administered to the mammal.

8. The method of claim 5 , wherein the compound is administered to the mammal in a given period of time before or after the at least one additional therapeutic agent is administered to the mammal.

9. The method of claim 1 , wherein the compound is formulated in a pharmaceutical composition that comprises at least one pharmaceutically acceptable excipient or carrier.

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

Assignees

• Univ Drexel

Inventors

• Kortagere Sandhya
• Artlett Carol M

Classifications

• A61K45/06

  Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

• C07C237/52

  having the nitrogen atom of at least one of the carboxamide groups further acylated · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• C07D211/90

  Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen · CPC title

• C07C2601/14

  The ring being saturated · CPC title