IP Library › Granted Patent US 12,636,308
Granted Patent B2
US 12,636,308 · App. 19/187,241 · Granted May 26, 2026

Storage stable formulations of sulfated glycosaminoglycans and fragments derived therefrom for the treatment of pain and other medical conditions

Inventors: Thomas Michael Vaughn (Franklin, TN); Joshua Alan Harrison (Jonesborough, TN); Karl F. Popp (Schodack Landing, NY); David J. Fairfax (Slingerlands, NY); Thomas Edward D'Ambra (Big Torch Key, FL); John Quinn (Troy, NY)
Assignee: ADORA ANIMAL HEALTH CORPORATION
A61K31/737A61K9/0014A61K9/06A61K45/06A61P19/02A61P29/00
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Quick Facts
Patent No.
US 12,636,308
App. No.
19/187,241
Granted
May 26, 2026
Kind
B2
Abstract

One aspect of the present application relates to a storage stable pharmaceutical composition comprising a sulfated glycosaminoglycan having an average molecular weight ranging from 3,000 to 15,000 Daltons, and a pharmaceutical carrier, where the pharmaceutical carrier is mixed with the sulfated glycosaminoglycan, as well as this composition's use in a method of treating a subject for a medically observable improvement. Another aspect of the present application relates to a process for producing a storage stable purified sulfated glycosaminoglycan.

Claims (43)

1 . A pharmaceutical composition comprising:

a polysulfated glycosaminoglycan having an average molecular weight ranging from 3,000 to 15,000 Daltons;

a skin penetrating agent, wherein said skin penetrating agent promotes transdermal penetration of said polysulfated glycosaminoglycan when applied to intact skin surfaces, and is selected from the group consisting of emulsions, primary or secondary alcohols, polyoxy ethers of fatty acids, fatty acid esters, surfactants, fatty acids, and combinations thereof; and

a pharmaceutical carrier for topical application, said pharmaceutical carrier being mixed with said polysulfated glycosaminoglycan and said skin penetrating agent.

2 . The pharmaceutical composition of claim 1 , wherein said polysulfated glycosaminoglycan has an average molecular weight ranging from 7,000 to 9,500 Daltons.

3 . The pharmaceutical composition of claim 1 , wherein said polysulfated glycosaminoglycan comprises repeating disaccharide units of N-acetylgalactosamine and glucuronic acid.

4 . The pharmaceutical composition of claim 1 , wherein said polysulfated glycosaminoglycan has a sulfate to carboxylate ratio between 3:1 and 4:1.

5 . The pharmaceutical composition of claim 1 , wherein said polysulfated glycosaminoglycan is prepared from chondroitin sulfate.

6 . The pharmaceutical composition of claim 1 , wherein said polysulfated glycosaminoglycan comprises mucopolysaccharide polysulfate.

7 . The pharmaceutical composition of claim 1 , wherein said polysulfated glycosaminoglycan comprises a purified polysulfated glycosaminoglycan.

8 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan is prepared by a process comprising filtration and/or precipitation.

9 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan has been purified by precipitation from an alcoholic solvent.

10 . The pharmaceutical composition of claim 9 , wherein said purified polysulfated glycosaminoglycan has been purified by precipitation from methanol.

11 . The pharmaceutical composition of claim 9 , wherein said purified polysulfated glycosaminoglycan has been purified by precipitation from ethanol.

12 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan includes no more than 10 wt % of carbohydrates or other contaminants with a molecular weight below 1,000 Daltons.

13 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan includes no more than 20 wt % of carbohydrates or other contaminants with a molecular weight below 3,000 Daltons.

14 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan includes no more than 25 wt % of carbohydrates or other contaminants with a molecular weight below 5,000 Daltons.

15 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan contains less than 5,000 ppm of acetic acid.

16 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan contains less than 5,000 ppm of acetic acid after storage at room temperature for at least 12 months following initiation of storage.

17 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan maintains a white or off-white color after storage at room temperature for at least 6 months following initiation of storage.

18 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan maintains a white or off-white color after storage at room temperature for at least 12 months following initiation of storage.

19 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan is prepared by a process comprising subjecting a polysulfated glycosaminoglycan starting material containing components below 1,000 Daltons to filtration under conditions effective to reduce the amount of components below 1,000 Daltons in the starting material to produce a purified polysulfated glycosaminoglycan having an average molecular weight ranging from 3,000 to 15,000 Daltons, wherein the purified polysulfated glycosaminoglycan includes no more than 10 wt % of carbohydrates or other contaminants with a molecular weight below 1,000 Daltons.

20 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan is prepared by a process comprising subjecting a polysulfated glycosaminoglycan starting material containing components below 3,000 Daltons to filtration under conditions effective to reduce the amount of components below 3,000 Daltons in the starting material to produce a purified polysulfated glycosaminoglycan having an average molecular weight ranging from 3,000 to 15,000 Daltons, wherein the purified polysulfated glycosaminoglycan includes no more than 20 wt % of carbohydrates or other contaminants with a molecular weight below 3,000 Daltons.

21 . The pharmaceutical composition of claim 7 , wherein said purified polysulfated glycosaminoglycan is prepared by a process comprising subjecting a polysulfated glycosaminoglycan starting material containing components below 5,000 Daltons to filtration under conditions effective to reduce the amount of components below 5,000 Daltons in the starting material to produce a purified polysulfated glycosaminoglycan having an average molecular weight ranging from 3,000 to 15,000 Daltons, wherein the purified polysulfated glycosaminoglycan includes no more than 25 wt % of carbohydrates or other contaminants with a molecular weight below 5,000 Daltons.

22 . The pharmaceutical composition of claim 1 , wherein said skin penetrating agent is selected from the group consisting of anionic surface-active agents, cationic surface-active agents, nonionic surface-active agents, and combinations thereof.

23 . The pharmaceutical composition of claim 1 , wherein said skin penetrating agent is selected from the group consisting of primary or secondary alcohols, polyoxy ethers of fatty acids, fatty acid esters and combinations thereof.

24 . The pharmaceutical composition of claim 1 , wherein said skin penetrating agent is an oil-in-water emulsion comprising one or more of tocopherol acetate, an aloe derivative, a silicon derivative, a chelating agent, an emulsifier, and a polyol.

25 . The pharmaceutical composition of claim 1 further comprising a pharmaceutically active agent.

26 . The pharmaceutical composition of claim 25 , wherein said pharmaceutically active agent is selected from the group consisting of pharmaceutically acceptable free bases, salts, esters, ethers, or solvates of antibiotics, anti-infectives, antimycotics agents, steroids, cannabinoids, antihistamines, anti-inflammatory agents, antiparasitic agents, immunomodulators, antisense agents, antiviral agents, treatments for hyper- and hypo skin pigmentation disorders, anti-psoriatic agents, keratolytic agents, DNA synthesis inhibitors, cytotoxic agents, antithyroid agents, monoclonal antibody regulators, TNF alpha antagonists, immunoglobulins, metabolic regulators, antiangiogenic agents, protease inhibitors, anxiolytics, kinase regulators, cell growth regulators, enzymes, prostaglandins, peptides, analgesics, skin moisturizers, astringents, exfoliating agents, agents intended to protect the skin or modify its appearance or improve its rate of healing, and combinations thereof.

27 . The pharmaceutical composition of claim 1 further comprising:

an additive selected from the group consisting of adjuvants, gelling agents, thickeners, solvents, preservatives, pH modifiers, colorants, perfumes, flavors, propellants, absorbents, adsorbents, antioxidants, antimicrobial preservatives, and combinations thereof.

28 . The pharmaceutical composition of claim 1 , wherein said carrier is selected from the group consisting of a transdermal tape, a transdermal patch, an ointment, a cream, a gel, a paste, a collodion composition, a foam, a rapid dissolving solid, and a lotion.

29 . The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises 0.1 to 25 wt % of said polysulfated glycosaminoglycan, 20 to 60 wt % of said skin penetrating agent, and 20 to 80 wt % of said carrier.

30 . The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises 5 to 16 wt % of said polysulfated glycosaminoglycan, 25 to 55 wt % of said skin penetrating agent, and 25 to 75 wt % of said carrier.

31 . The pharmaceutical composition of claim 1 , wherein said composition is in a form suitable for topical application to skin.

32 . The pharmaceutical composition of claim 1 , wherein said composition is in a form suitable for topical application to mucosa.

33 . The pharmaceutical composition of claim 1 , wherein said composition is in a form suitable for delivery by aural, oral, ophthalmic, nasal, rectal, urethral, vaginal, dermal, buccal, or sublingual routes.

34 . The pharmaceutical composition of claim 1 , wherein said composition is in the form of an aerosol, a chewable bar, a bead, a capsule, a cellular sheet, a chewable gel, a concentrate, a cream, an elixir, an emulsion, an enema, a film, a gel, a chewing gum, an irrigant, a jelly, a liniment, a lipstick, a liquid, a lotion, a lozenge, a mouthwash, an oil, an ointment, a paste, a pastille, a patch, a pellet, a pill, a plaster, a poultice, a powder, a ring, a rinse, a salve, a shampoo, a soap, a solution, a sponge, a spray, a stick, a strip, a suppository, a suspension, a swab, a syrup, a tablet, a tampon, a tape, a tincture, a troche, a wafer, and/or combinations thereof.

35 . The pharmaceutical composition of claim 1 , wherein said skin penetrating agent is an emulsion.

36 . A pharmaceutical composition comprising:

a polysulfated glycosaminoglycan having an average molecular weight ranging from 3,000 to 15,000 Daltons, wherein said polysulfated glycosaminoglycan comprises less than 5 wt % of chondroitin sulfate;

a skin penetrating agent, wherein said skin penetrating agent promotes transdermal penetration of said polysulfated glycosaminoglycan when applied to intact skin surfaces, and is selected from the group consisting of emulsions, primary or secondary alcohols, polyoxy ethers of fatty acids, fatty acid esters, surfactants, fatty acids, and combinations thereof; and

a pharmaceutical carrier for topical application, said pharmaceutical carrier being mixed with said polysulfated glycosaminoglycan and said skin penetrating agent.

Assignments (1)
CHANGE OF NAME Recorded May 7, 2026
From: ADORA ANIMAL HEALTH CORPORATION
To: ADORA LIFE SCIENCE, INC.
Reel/Frame 074586/0171 →
Continuity (4)
Continuation 18750691 · Jun 21, 2024
Division 18476580 · Sep 28, 2023
Provisional Application 63411363 · Sep 29, 2022
Related Publication 20250249030A1 · Aug 7, 2025
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