IP Library Granted Patent US 8,940,755
Granted Patent B2
US 8,940,755 · App. 11/001,979 · Granted Jan 27, 2015

Therapeutic combinations and methods including IRM compounds

Inventors: Mark A. Tomai (Woodbury, MN); Gary W. Gullikson (Stillwater, MN); David M. Hammerbeck (Houlton, WI); Elaine A. Egging (Woodbury, MN); Michael J. Reiter (New Richmond, WI); Christopher D. Gram (River Falls, WI); John P. Vasilakos (Woodbury, MN)
Assignee: 3M Innovative Properties Company
A61K45/06A61K31/00
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Quick Facts
Patent No.
US 8,940,755
App. No.
11/001,979
Granted
Jan 27, 2015
Kind
B2
Abstract

The present invention provides therapeutic combinations that include an immune response modifier (IRM) component and an anti-inflammatory component. The inventions further provide methods of treating a condition by administering to one having the condition a therapeutic combination that includes an IRM component and an anti-inflammatory component.

Claims (20)

1. A method of treating neoplastic tumors, comprising administering to a subject having the neoplastic tumors a therapeutic combination that comprises

(a) an IRM compound agonist of at least one of TLR7 or TLR8 in an amount effective to treat the neoplastic tumors, where the IRM compound comprises an imidazoquinoline amine, a tetrahydroimidazoquinoline amine, an imidazopyridine amine, a 1,2-bridged imidazoquinoline amine, a 6,7-fused cycloalkylimidazopyridine amine, an imidazonaphthyridine amine, a tetrahydroimidazonaphthyridine amine, an oxazoloquinoline amine, a thiazoloquinoline amine, an oxazolopyridine amine, a thiazolopyridine amine, an oxazolonaphthyridine amine, or a thiazolonaphthyridine amine; and

(b) an anti-inflammatory compound in an amount effective to limit a side effect of administering the IRM compound, wherein the anti-inflammatory compound comprises a glucocorticoid.

2. The method of claim 1 wherein the IRM compound and the anti-inflammatory compound are administered at different sites.

3. The method of claim 1 wherein the IRM compound and the anti-inflammatory compound are administered at different times.

4. The method of claim 1 , wherein the IRM compound is other than 1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine.

5. The method of claim 1 , wherein the imidazoquinoline amine is a amide substituted imidazoquinoline amine, sulfonamide substituted imidazoquinoline amine, urea substituted imidazoquinoline amine, aryl ether substituted imidazoquinoline amine, heterocyclic ether substituted imidazoquinoline amine, amido ether substituted imidazoquinoline amine, sulfonamido ether substituted imidazoquinoline amine, urea substituted imidazoquinoline ether, thioether substituted imidazoquinoline amine, or a 6-, 7-, 8-, or 9-aryl, heteroaryl, aryloxy or arylalkyleneoxy substituted imidazoquinoline amine.

6. The method of claim 1 , wherein the neoplastic tumors are from basal cell carcinoma or actinic keratosis.

7. A method of treating neoplastic tumors, comprising administering to a subject having the neoplastic tumors a therapeutic combination that comprises

(a) an IRM compound agonist of at least one of TLR7 or TLR8 in an amount effective to treat the neoplastic tumors, where the IRM compound comprises a substituted imidazoquinoline amine, a tetrahydroimidazoquinoline amine, an imidazopyridine amine, a 1,2-bridged imidazoquinoline amine, a 6,7-fused cycloalkylimidazopyridine amine, an imidazonaphthyridine amine, a tetrahydroimidazonaphthyridine amine, an oxazoloquinoline amine, a thiazoloquinoline amine, an oxazolopyridine amine, a thiazolopyridine amine, an oxazolonaphthyridine amine, or a thiazolonaphthyridine amine; and

(b) an anti-inflammatory compound in an amount effective to limit a side effect of administering the IRM compound,

wherein the substituted imidazoquinoline amine is a amide substituted imidazoquinoline amine, sulfonamide substituted imidazoquinoline amine, urea substituted imidazoquinoline amine, aryl ether substituted imidazoquinoline amine, heterocyclic ether substituted imidazoquinoline amine, amido ether substituted imidazoquinoline amine, sulfonamido ether substituted imidazoquinoline amine, urea substituted imidazoquinoline ether, thioether substituted imidazoquinoline amine, or a 6-, 7-, 8-, or 9-aryl, heteroaryl, aryloxy or arylalkyleneoxy substituted imidazoquinoline amine.

8. The method of claim 7 , wherein the IRM compound and the anti-inflammatory compound are administered at different sites.

9. The method of claim 7 , wherein the IRM compound and the anti-inflammatory compound are administered at different times.

10. The method of claim 7 , wherein the neoplastic tumors are from basal cell carcinoma or actinic keratosis.

11. A method of treating warts, basal cell carcinoma or actinic keratosis, comprising administering to a subject having the warts, basal cell carcinoma or actinic keratosis a therapeutic combination that comprises

(a) an IRM compound agonist of at least one of TLR7 or TLR8 in an amount effective to treat the warts, basal cell carcinoma or actinic keratosis, where the IRM compound comprises an imidazoquinoline amine, a tetrahydroimidazoquinoline amine, an imidazopyridine amine, a 1,2-bridged imidazoquinoline amine, a 6,7-fused cycloalkylimidazopyridine amine, an imidazonaphthyridine amine, a tetrahydroimidazonaphthyridine amine, an oxazoloquinoline amine, a thiazoloquinoline amine, an oxazolopyridine amine, a thiazolopyridine amine, an oxazolonaphthyridine amine, or a thiazolonaphthyridine amine; and

(b) an anti-inflammatory compound in an amount effective to limit a side effect of administering the IRM compound.

12. The method of claim 11 , wherein the IRM compound and the anti-inflammatory compound are administered at different sites.

13. The method of claim 11 , wherein the IRM compound and the anti-inflammatory compound are administered at different times.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2014
From: TOMAI, MARK A.; GULLIKSON, GARY W.; HAMMERBECK, DAVID M.; EGGING, ELAINE A.; REITER, MICHAEL J.; GRAM, CHRISTOPHER D.; VASILAKOS, JOHN P.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 033744/0676 →
Continuity (2)
Provisional Application 60526240 · Dec 2, 2003
Related Publication 20050171072A1 · Aug 4, 2005