IP Library Granted Patent US 9,205,067
Granted Patent B2
US 9,205,067 · App. 14/562,608 · Granted Dec 8, 2015

Compounds for treating inflammation and pain

Inventors: Joseph P. St. Laurent (Lakeville, MA); Gerald S. Jones (Norwood, MA); David M. Bresse (Middleboro, MA)
Assignee: OLATEC INDUSTRIES LLC
A61K31/16A61K9/0014A61K9/06A61K31/145A61K47/08A61K47/14
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,205,067
App. No.
14/562,608
Granted
Dec 8, 2015
Kind
B2
Abstract

The present invention is directed to a pharmaceutical composition comprising a pharmaceutically acceptable carrier and ω-(methylsulfonyl)alkylamine or ω-(methylsulfonyl)alkylamide. The present invention is also directed to a method for treating inflammation, inflammatory-related disorders, or pain, by administering ω-(methylsulfonyl)alkylamine or ω-(methylsulfonyl)alkylamide, or a pharmaceutically acceptable salt or solvate thereof to a subject in need thereof.

Claims (35)

1. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a compound of A or a pharmaceutically acceptable salt thereof:

wherein the compound has at least 90% (w/w) purity, and the composition is in a topical form of gels, creams, lotions, ointments, or patches.

2. The pharmaceutical composition according to claim l, wherein the pharmaceutically acceptable carrier is an emollient selected from the group consisting of: lauryl lactate, diethylene glycol monoethyl ether, caprylic/capric triglyceride, octisalate, silicone fluid, squalene, and sunflower oil.

3. The pharmaceutical composition according to claim 1 , wherein the pharmaceutically acceptable carrier is a permeation enhancer selected from the group consisting of lactate esters and diethylene glycol monoethyl ether.

4. The pharmaceutical composition according to claim 3 , further comprising acrylates/C10-30 alkyl and tris(2-hydroxyethyl)amine.

5. A method of treating inflammation or pain, comprising the steps of:

topically identifying a subject suffering from inflammation or pain, and

administering to the subject the pharmaceutical composition of claim 1 , in an amount effective to treat inflammation or pain.

6. The method according to claim 5 , wherein said method reduces or alleviates the symptoms of localized manifestations of inflammation characterized by acute or chronic swelling, pain, or redness.

7. The method according to claim 5 , wherein said inflammation and/or pain is associated with a skeletal or muscular disease or condition selected from the group consisting of: musculoskeletal sprains, musculoskeletal strains, tendonopathy, peripheral radiculopathy, osteoarthritis, degenerative joint disease, juvenile arthritis, gout, ankylosing spondylitis, psoriatic arthritis, system lupus erythematosus, costochondritis, tendonitis, bursitis, temporomandibular joint syndrome, and fibromyalgia.

8. The method according to claim 5 , wherein said inflammation and/or pain is associated with joints, ligaments, tendons, bone, muscles, or fascia.

9. The method according to claim 5 , wherein said inflammation and/or pain is associated with dermatitis or psoriasis.

10. The method according to claim 9 , wherein said dermatitis is atopic dermatitis or contact dermatitis.

11. A method of treating an inflammatory skin disease or disorder, comprising the steps of:

identifying a subject suffering from an inflammatory skin disease or disorder, and

administering to the subject the pharmaceutical composition of claim 1 , in an amount effective to treat the inflammatory skin disease or disorder, wherein the inflammatory skin disease or disorder is dermatitis, psoriasis, or acne.

12. The method according to claim 11 , for treating atopic dermatitis and alleviating one or more symptoms selected from the group consisting of erythema, induration, lichenification, scaling, and oozing and crusting.

13. The method according to claim 11 , for treating psoriasis and alleviating one or more symptoms selected from the group consisting of erythema, scaling, and/or thickness of the psoriasis lesions.

14. The method according to claim 11 , for treating acne and alleviating acne lesions selected from the groups consisting of closed comedones, papules, pustules, nodules, and cysts.

15. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a compound of A or a pharmaceutically acceptable salt thereof:

wherein the compound has at least 90% (w/w) purity, and the composition is in an oral form of tablets, capsules, or syrup.

16. A method of treating inflammation or pain, comprising the steps of:

identifying a subject suffering from inflammation or pain, and

orally administering to the subject the pharmaceutical composition of claim 15 , in an amount effective to treat inflammation or pain.

17. The method according to claim 15 , wherein said method reduces or alleviates the symptoms of localized manifestations of inflammation characterized by acute or chronic swelling, pain, or redness.

18. The method according to claim 15 , wherein said inflammation and/or pain is associated with a skeletal or muscular disease or condition selected from the group consisting of: musculoskeletal sprains, musculoskeletal strains, tendonopathy, peripheral radiculopathy, osteoarthritis, degenerative joint disease, juvenile arthritis, gout, ankylosing spondylitis, psoriatic arthritis, system lupus erythematosus, costochondritis, tendonitis, bursitis, temporomandibular joint syndrome, and fibromyalgia.

19. The method according to claim 15 , wherein said inflammation and/or pain is associated with joints, ligaments, tendons, bone, muscles, or fascia.

20. The method according to claim 15 , wherein said inflammation and/or pain is associated with dermatitis or psoriasis.

21. The method according to claim 20 , wherein said dermatitis is atopic dermatitis or contact dermatitis.

22. A method of treating an inflammatory skin disease or disorder, comprising the steps of:

identifying a subject suffering from an inflammatory skin disease or disorder, and

administering to the subject the pharmaceutical composition of claim 15 , in an amount effective to treat the inflammatory skin disease or disorder, wherein the inflammatory skin disease or disorder is dermatitis, psoriasis, or acne.

23. The method according to claim 22 , for treating atopic dermatitis and alleviating one or more symptoms selected from the group consisting of erythema, induration, lichenification, scaling, and oozing and crusting.

24. The method according to claim 22 , for treating psoriasis and alleviating one or more symptoms selected from the group consisting of erythema, scaling, and/or thickness of the psoriasis lesions.

25. The method according to claim 23 , for treating acne and alleviating acne lesions selected from the groups consisting of closed comedones, papules, pustules, nodules, and cysts.

Assignments (3)
CHANGE OF NAME Recorded Nov 7, 2023
From: OLATEC THERAPEUTICS LLC
To: OLATEC THERAPEUTICS, INC.
Reel/Frame 065489/0809 →
CHANGE OF NAME Recorded Mar 18, 2016
From: OLATEC INDUSTRIES LLC
To: OLATEC THERAPEUTICS LLC
Reel/Frame 038177/0824 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2015
From: ST. LAURENT, JOSEPH P.; JONES, GERALD S.; BRESSE, DAVID M.
To: OLATEC INDUSTRIES LLC
Reel/Frame 036333/0346 →
Continuity (3)
Continuation PCTUS2013044575 · Jun 6, 2013
Provisional Application 61658251 · Jun 11, 2012
Related Publication 20150094373A1 · Apr 2, 2015