Methods for the prevention or treatment of cytokine storm

Patent metadata

Field	Value
Publication number	US-12485107-B2
Application number	US-202017421785-A
Country	US
Kind code	B2
Filing date	Jan 10, 2020
Priority date	Jan 11, 2019
Publication date	Dec 2, 2025
Grant date	Dec 2, 2025

Abstract

The invention provides methods for treating, suppressing, or preventing detrimental cytokine and/or lipid mediator surges that can result from a variety of different diseases, conditions, and therapeutic treatments, e.g., by inhibition of cyclooxygenase-2 (COX-2) and soluble epoxide hydrolase (sEH).

First claim

The invention claimed is:

1 . A method of preventing a cytokine or lipid surge in a subject under treatment for cancer, the method comprising administering to the subject a dual inhibitor of cyclooxygenase-2 (COX-2) and soluble epoxide hydrolase (sEH), or an inhibitor of COX-2 and an inhibitor of sEH, wherein:
a) the dual inhibitor of COX-2 and sEH is selected from the group consisting of PTUPB, 1-Adamantan-1-yl-3-[1-(4-methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-urea, 1-Cycloheptyl-3-[1-(4-methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-phenyl-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-(4-trifluoromethoxy-phenyl)-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-(4-trifluoromethyl-phenyl)-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-(3-trifluoromethyl-phenyl)-urea, 4-{5-Phenyl-3-[3-(3-trifluoromethyl-phenyl)-ureidomethyl]-pyrazol-1-yl}-benzenesulfonamide, 1-[5-tert-Butyl-1-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-ylmethyl]-3-(3-trifluoromethyl-phenyl)-urea, 4-{5-Phenyl-3-[3-(3-trifluoromethyl-phenyl)-ureido]-pyrazol-1-yl}-benzenesulfonamide, 4-(5-Phenyl-3-{2-[3-(3-trifluoromethyl-phenyl)-ureido]-ethyl}-pyrazol-1-yl)-benzenesulfonamide, 1-{3-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-yl]-propyl}-3-(3-trifluoromethyl-phenyl)-urea, 4-(5-Phenyl-3-{3-[3-(3-trifluoromethyl-phenyl)-ureido]-propyl}-pyrazol-1-yl)-benzenesulfonamide, 4-(5-p-Tolyl-3-{3-[3-(3-trifluoromethyl-phenyl)-ureido]-propyl}-pyrazol-1-yl)-benzenesulfonamide, 4-(3-{3-[3-(2,6-Diisopropyl-phenyl)-ureido]-propyl}-5-phenyl-pyrazol-1-yl)-benzenesulfonamide, 4-{5-Phenyl-3-[3-(3-phenyl-ureido)-propyl]-pyrazol-1-yl}-benzenesulfonamide, 4-{3-[3-(3-Adamantan-1-yl-ureido)-propyl]-5-phenyl-pyrazol-1-yl}-benzenesulfonamide, 4-{3-[3-(3-Cycloheptyl-ureido)-propyl]-5-phenyl-pyrazol-1-yl}-benzenesulfonamide, 4-(3-{3-[3-(4-Chloro-phenyl)-ureido]-propyl}-5-phenyl-pyrazol-1-yl)-benzenesulfonamide, and 4-(5-Phenyl-3-{3-[3-(4-trifluoromethoxy-phenyl)-ureido]-propyl}-pyrazol-1-yl)-benzenesulfonamide; b) the inhibitor of COX-2 is selected from the group consisting of Aspirin, Ibuprofen, Naproxen, Ketorolac, Indomethacin, Diclofenac, Piroxicam, Mefenamic acid, Nimesulide, celecoxib, rofecoxib, FR122047, and SC-560; and c) the inhibitor of sEH is selected from the group consisting of t-AUCB, AUDA, AEPU, APAU, TUCF, TPAU, c-AUCB, c-TUCB, TUPS, t-TUCB, TPPU, t-CUCB, t-MTUCB, t-CUCMB, t-CUPM, t-TPUCB, ITPU, BPTU, TCC, GSK2256294, and Ome-21i.

2 . The method of claim 1 , wherein the cytokine or lipid surge results from infection by a bacterium, virus, fungus, or parasite.

3 . The method of claim 2 , wherein the cytokine or lipid surge results from infection by a bacterium.

4 . The method of claim 2 , wherein the cytokine or lipid surge results from infection by a virus.

5 . The method of claim 2 , wherein the cytokine or lipid surge results from infection by a parasite.

6 . The method of claim 2 , wherein the subject has or is at risk of developing a severe reaction to infection.

7 . The method of claim 1 , wherein the cytokine or lipid surge results from a condition resulting in damage or insult to the body or a non-infectious disease process.

8 . The method of claim 7 , wherein the cytokine or lipid surge results from trauma, injury, burn, exposure to toxic materials, acute respiratory distress syndrome secondary to drug use or inhalation of toxins, cancer, acute pancreatitis or hepatitis, fulminant hepatic failure, multiple sclerosis, rheumatic diseases, or Langerhans cell histiocytosis (LCH).

9 . The method of claim 8 , wherein the toxic material is a bacterial or a fungal toxin.

10 . The method of claim 8 , wherein the toxic material is a carcinogen.

11 . The method of claim 1 , wherein the cytokine or lipid surge results from the treatment of a disease or condition of the subject.

12 . The method of claim 1 , wherein administration of the dual inhibitor of COX-2 and sEH, or the inhibitor of COX-2 and the inhibitor of sEH, reduces the level of one or more of a pro-inflammatory cytokine, a proangiogenic cytokine, and/or a bioactive lipid.

13 . The method of claim 1 , wherein the subject is co-administered a chemotherapeutic agent and/or an immunotherapeutic agent.

14 . The method of claim 1 , wherein the subject has or is at risk of developing cancer or a metastasis thereof.

15 . The method of claim 1 , wherein the inhibitor of COX-2 is selected from the group consisting of Aspirin, Ibuprofen, Naproxen, Ketorolac, Indomethacin, Diclofenac, Piroxicam, Mefenamic acid, Nimesulide, celecoxib, rofecoxib, FR122047, and SC-560 and the inhibitor of sEH is selected from the group consisting of t-AUCB, AUDA, AEPU, APAU, TUCF, TPAU, c-AUCB, c-TUCB, TUPS, t-TUCB, TPPU, t-CUCB, t-MTUCB, t-CUCMB, t-CUPM, t-TPUCB, ITPU, BPTU, TCC, GSK2256294, and Ome-21i.

16 . A method of treating or suppressing a cytokine or lipid surge in a subject under treatment for cancer, the method comprising administering to the subject a dual inhibitor of COX-2 and sEH, or an inhibitor of COX-2 and an inhibitor of sEH, wherein:
a) the dual inhibitor of COX-2 and sEH is selected from the group consisting of PTUPB, 1-Adamantan-1-yl-3-[1-(4-methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-urea, 1-Cycloheptyl-3-[1-(4-methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-phenyl-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-(4-trifluoromethoxy-phenyl)-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-(4-trifluoromethyl-phenyl)-urea, 1-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-ylmethyl]-3-(3-trifluoromethyl-phenyl)-urea, 4-{5-Phenyl-3-[3-(3-trifluoromethyl-phenyl)-ureidomethyl]-pyrazol-1-yl}-benzenesulfonamide, 1-[5-tert-Butyl-1-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-ylmethyl]-3-(3-trifluoromethyl-phenyl)-urea, 4-{5-Phenyl-3-[3-(3-trifluoromethyl-phenyl)-ureido]-pyrazol-1-yl}-benzenesulfonamide, 4-(5-Phenyl-3-{2-[3-(3-trifluoromethyl-phenyl)-ureido]-ethyl}-pyrazol-1-yl)-benzenesulfonamide, 1-{3-[1-(4-Methanesulfonyl-phenyl)-5-phenyl-1H-pyrazol-3-yl]-propyl}-3-(3-trifluoromethyl-phenyl)-urea, 4-(5-Phenyl-3-{3-[3-(3-trifluoromethyl-phenyl)-ureido]-propyl}-pyrazol-1-yl)-benzenesulfonamide, 4-(5-p-Tolyl-3-{3-[3-(3-trifluoromethyl-phenyl)-ureido]-propyl}-pyrazol-1-yl)-benzenesulfonamide, 4-(3-{3-[3-(2,6-Diisopropyl-phenyl)-ureido]-propyl}-5-phenyl-pyrazol-1-yl)-benzenesulfonamide, 4-{5-Phenyl-3-[3-(3-phenyl-ureido)-propyl]-pyrazol-1-yl}-benzenesulfonamide, 4-{3-[3-(3-Adamantan-1-yl-ureido)-propyl]-5-phenyl-pyrazol-1-yl}-benzenesulfonamide, 4-{3-[3-(3-Cycloheptyl-ureido)-propyl]-5-phenyl-pyrazol-1-yl}-benzenesulfonamide, 4-(3-{3-[3-(4-Chloro-phenyl)-ureido]-propyl}-5-phenyl-pyrazol-1-yl)-benzenesulfonamide, and 4-(5-Phenyl-3-{3-[3-(4-trifluoromethoxy-phenyl)-ureido]-propyl}-pyrazol-1-yl)-benzenesulfonamide; b) the inhibitor of COX-2 is selected from the group consisting of Aspirin, Ibuprofen, Naproxen, Ketorolac, Indomethacin, Diclofenac, Piroxicam, Mefenamic acid, Nimesulide, celecoxib, rofecoxib, FR122047, and SC-560; and c) the inhibitor of sEH is selected from the group consisting of t-AUCB, AUDA, AEPU, APAU, TUCF, TPAU, c-AUCB, c-TUCB, TUPS, t-TUCB, TPPU, t-CUCB, t-MTUCB, t-CUCMB, t-CUPM, t-TPUCB, ITPU, BPTU, TCC, GSK2256294, and Ome-21i.

17 . The method of claim 16 , comprising administration of PTUPB.

18 . The method of claim 1 , whe

Assignees

• Beth Israel Deaconess Medical Ct Inc
• Univ California

Inventors

• Panigrahy Dipak
• Gartung Allison
• Fishbein Anna
• Hammock Bruce
• Hwang Sung Hee
• Sukhatme Vikas P

Classifications

• A61K31/415

  1,2-Diazoles · CPC title

• A61K31/196

  the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61P37/06

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

• A61K31/18

  Sulfonamides (compounds containing a para-N-benzene-sulfonyl-N- group A61K31/63) · CPC title