IP Library Granted Patent US 10,940,126
Granted Patent B2
US 10,940,126 · App. 15/393,380 · Granted Mar 9, 2021

Inhibition of IL-8 in the treatment of pain and/or bone loss

Inventors: Camilla Svensson (Stockholm, SE); Lars Klareskog (Stockholm, SE); Vivianne Malmstrom (Stockholm, SE); Anca Catrina (Taby, SE)
A61K31/18A61K31/185A61K31/341A61K31/4462A61K31/495A61K31/498A61K31/519G01N33/6869G06F19/00G16H10/20G01N2333/5421G01N2800/2842G01N2800/52Y02A90/10
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Quick Facts
Patent No.
US 10,940,126
App. No.
15/393,380
Granted
Mar 9, 2021
Kind
B2
Abstract

Pain associated with a contribution of IL-8 and osteoclasts in a subject is prevented, treated and/or alleviated by the administration of an effective amount of a compound capable of inhibiting or blocking the action of interleukin 8 (IL-8). Methods and compounds for this use are disclosed, as well as a diagnostic method and kit.

Claims (36)

1. A method of alleviating joint pain without concurrent synovitis in a subject in need thereof, said method comprising administering to the subject an effective amount of a compound capable of inhibiting or blocking the action of IL-8,

wherein said joint pain without concurrent synovitis is associated with a presence of IL-8 and osteoclasts in the subject,

and

wherein said compound is selected from the group consisting of

reparixin (repertaxin, (2R)-2-[4-(2-methylpropyl)phenyl]-N-methylsulfonylpropanamide);

DF 2162 (4-[(1R)-2-amino-1-methyl-2-oxoetthyl]phenyl trifluoromethane sulfonate);

AZD8309 (5-[[(2,3-difluorophenyl)methyl]thio]-7[[(1R)-2-hydroxy-1-methylethyl]amino]-thiazolo[4,5-d]pyrimidin-2(3H-one);

AZD5069 (N-[2-[[2,3-difluorophenyl)methyl]thio]-6-{[(1r,2s)-2,3-dihydroxy-1-methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide);

PD0220245 (N-(3-[2,2′-bithiophen-5-yl]-6,7-dichloro-2-quinoxalinyl)-N,N-diethyl-butane-1,4-diamine dihydrochloride);

SB-332235 (1-(4-chloro-2-hydroxy-3-sulfamoylphenyl)-3-(2,3-dichlorophenyl)urea);

SCH-527123 (navarixin, 2-hydroxy-N,N-dimethyl-3-[[2-[[(1R)-1-(5-methylfuran-2-yl)propyl]amino]-3,4-dioxocyclobuten-1-yl]amino]benzamide);

SB-656933 (elubrixin, 1-(2-chloro-3-fluorophenyl)-3-(4-chloro-2-hydroxy-3-piperazin-1-ylsulfonylphenyl)urea);

SB-225002 (N-(2-bromophenyl)-N′-(2-hydroxy-4-nitrophenyl)urea); and

GSK1325756 (danirixin, 1-[4-chloro-2-hydroxy-3-[(3S)-piperidin-3-yl]sulfonylphenyl]-3-(3-fluoro-2-methylphenyl)urea).

2. The method according to claim 1 , wherein said compound is reparixin (repertaxin, (2R)-2-[4-(2-methylpropyl)phenyl]-N-methylsulfonylpropanamide).

3. The method according to claim 1 , wherein said compound is danirixin (1-[4-chloro-2-hydroxy-3-[(3S)-piperidin-3-yl]sulfonylphenyl]-3-(3-fluoro-2-methylphenyl)urea.

4. A method of alleviating joint pain without concurrent synovitis in a subject in need thereof, said method comprising administering to the subject an effective amount of a compound capable of inhibiting or blocking the action of IL-8,

wherein said joint pain without concurrent synovitis is associated with a presence of IL-8 and osteoclasts in the subject,

wherein IL-8 activation of the osteoclasts is associated with a presence of autoantibodies in said subject,

and

wherein said compound is selected from the group consisting of

reparixin (repertaxin, (2R)-2-[4-(2-methylpropyl)phenyl]-N-methylsulfonylpropanamide);

DF 2162 (4-[(1R)-2-amino-1-methyl-2-oxoetthyl]phenyl trifluoromethane sulfonate);

AZD8309 (5-[[(2,3-difluorophenyl)methyl]thio]-7[[(1R)-2-hydroxy-1-methylethyl]amino]-thiazolo[4,5-d]pyrimidin-2(3H-one);

AZD5069 (N-[2-[[2,3-difluorophenyl)methyl]thio]-6-{[(1r,2s)-2,3-dihydroxy-1-methylpropyl]oxy}-4-pyrimidinyl]-1-azetidinesulfonamide);

PD0220245 (N-(3-[2,2′-bithiophen-5-yl]-6,7-dichloro-2-quinoxalinyl)-N,N-diethyl-butane-1,4-diamine dihydrochloride);

SB-332235 (1-(4-chloro-2-hydroxy-3-sulfamoylphenyl)-3-(2,3-dichlorophenyl)urea);

SCH-527123 (navarixin, 2-hydroxy-N,N-dimethyl-3-[[2-[[1 R)-1-(5-methylfuran-2-yl)propyl]amino]-3,4-dioxocyclobuten-1-yl]amino]benzamide);

SB-656933 (elubrixin, 1-(2-chloro-3-fluorophenyl)-3-(4-chloro-2-hydroxy-3-piperazin-1-ylsulfonylphenyl)urea);

SB-225002 (N-(2-bromophenyl)-N′-(2-hydroxy-4-nitrophenyl)urea); and

GSK1325756 (danirixin, 1-[4-chloro-2-hydroxy-3-[3S)-piperidin-3-yl]sulfonylphenyl]-3-(3-fluoro-2-methylphenyl)urea).

5. The method according to claim 4 , wherein said autoantibodies are anti-citrullinated protein antibodies (ACPA).

6. The method according to claim 4 , wherein said compound is reparixin (repertaxin, (2R)-2-[4-(2-methylpropyl)phenyl]-N-methylsulfonylpropanamide).

7. The method according to claim 4 , wherein said compound is danirixin, 1-[4-chloro-2-hydroxy-3-[(3S)-piperidin-3-yl]sulfonylphenyl]-3-(3-fluoro-2-methylphenyl)urea.

8. The method according to claim 4 , wherein said autoantibodies are detectable in a sample taken from said subject, using an enzyme-linked immunosorbent assay (ELISA) for qualitative and semi-qualitative determination of IgG antibodies to Cyclic Citrullinated Peptides (CCP).

9. The method according to claim 8 , wherein said subject is suffering from an autoimmune disease selected from rheumatoid arthritis, osteoarthritis, and arthralgia.

Continuity (9)
Continuation PCTSE2016050664 · Jun 30, 2016
Provisional Application 62188499 · Jul 3, 2015
Provisional Application 62221119 · Sep 21, 2015
Provisional Application 62221122 · Sep 21, 2015
Provisional Application 62221133 · Sep 21, 2015
Provisional Application 62221134 · Sep 21, 2015
Provisional Application 62303452 · Mar 4, 2015
Provisional Application 62321486 · Apr 12, 2016
Related Publication 20170181987A1 · Jun 29, 2017