IP Library › Granted Patent US 11,541,075
Granted Patent B2
US 11,541,075 · App. 17/002,847 · Granted Jan 3, 2023

Treatment of arthritis and other musculoskeletal disorders with crosslinked hyaluronic acid

Inventors: Tamera B. Gooding (Jamaica Plain, MA); Stephen J. Kennedy (Hudson, MA); Charles H. Sherwood (Sudbury, MA)
A61K31/728A61K9/0019A61K9/0024A61K9/06A61K31/573A61K31/729A61K35/28A61K35/32A61K38/1841A61K45/06A61K47/36A61L27/20A61L27/227A61L27/3817A61L27/3834A61L27/3843A61L27/48A61L27/52A61L27/56A61M5/178C08L5/08A61L2430/06
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Quick Facts
Patent No.
US 11,541,075
App. No.
17/002,847
Filed
Aug 26, 2020
Granted
Jan 3, 2023
Kind
B2
Art Unit
1623
USPC
424/130.1
Abstract

A method of treating a subject having a musculoskeletal disorder includes administering to a subject's articular site in need thereof an effective amount of a hyaluronic acid (HA) composition. In one embodiment, the HA composition includes an HA derivative, wherein carboxyl functionalities of the hyaluronic acid derivative are each independently derivatized to include an N-acylurea or O-acyl isourea, or both N-acylurea and O-acyl isourea. In another embodiment, the HA composition includes a crosslinked HA gel that is prepared by reacting an uncrosslinked HA with a biscarbodiimide in the presence of pH buffer in a range of between about 4 and about 8. The composite can optionally include at least one second bioactive agent other than the HA derivative, such as a steroid.

Claims (33)

1. A method of treating a subject having a musculoskeletal disorder, comprising administering to a subject's articular site in need thereof an effective amount of a hyaluronic acid (HA) composition that includes a hyaluronic acid derivative and triamcinolone hexacetonide, wherein carboxyl functionalities of the hyaluronic acid derivative are each independently derivatized to include an N-acylurea or O-acyl isourea, or both N-acylurea and O-acyl isourea, wherein the HA composition includes a crosslinked HA gel that includes at least one crosslink represented by the following structural formula:

HA′-U-R 2 -U-HA′

wherein:

each HA′ is a hyaluronic acid that is the same or different;

each U is independently an optionally substituted O-acyl isourea or N-acyl urea; and

each R 2 is independently a substituted or unsubstituted hydrocarbylene group optionally interrupted by one or more heteroatoms.

2. The method of claim 1 , wherein the musculoskeletal disorder is osteoarthritis.

3. A method of treating a subject having a musculoskeletal disorder, comprising the steps of:

(a) inserting a needle into a subject's articular site in need thereof, wherein the needle is coupled to a syringe loaded with an effective amount of a hyaluronic acid (HA) composition that includes an HA derivative and triamcinolone hexacetonide, wherein carboxyl functionalities of the hyaluronic acid derivative are each independently derivatized to include an N-acylurea or O-acyl isourea, or both N-acylurea and O-acyl isourea; and

(b) applying force to the syringe, whereby at least a portion of the HA composition is delivered to the articular site of the subject;

wherein the hyaluronic acid composition includes a crosslinked HA gel that includes at least one crosslink represented by the following structural formula:

HA′-U-R 2 -U-HA′

wherein:

each HA′ is a hyaluronic acid that is the same or different;

each U is independently an optionally substituted O-acyl isourea or N-acyl urea; and

each R 2 is independently a substituted or unsubstituted hydrocarbylene group optionally interrupted by one or more heteroatoms.

4. The method of claim 3 , wherein the musculoskeletal disorder is osteoarthritis.

5. The method of claim 1 , wherein the at least one crosslink is represented by the following structural formula:

6. The method of claim 1 , wherein between about 1% and about 10% by mol of the carboxyl functionalities of the crosslinked HA gel is crosslinked.

7. The method of claim 1 , wherein the HA composition is formulated for administration as an intra-articular injection.

8. The method of claim 1 , wherein the HA composition comprises about 2 mg/mL to about 30 mg/mL of the HA derivative.

9. The method of claim 1 , which provides rapid and prolonged pain relief.

10. The method of claim 1 , which provides pain relief for about 4-6 months.

11. The method of claim 1 , wherein the at least one crosslink is an intermolecular crosslink.

12. The method of claim 1 , wherein the at least one crosslink is an intramolecular crosslink.

13. The method of claim 3 , wherein the at least one crosslink is represented by the following structural formula:

14. The method of claim 3 , wherein between about 1% and about 10% by mol of the carboxyl functionalities of the crosslinked HA gel is crosslinked.

15. The method of claim 3 , wherein the HA composition is formulated for administration as an intra-articular injection.

16. The method of claim 3 , wherein the HA composition comprises about 2 mg/mL to about 30 mg/mL of the HA derivative.

17. The method of claim 3 , wherein the syringe comprises about 4 mL of the HA composition.

18. The method of claim 3 , wherein the syringe is a 5-mL syringe.

19. The method of claim 3 , wherein the syringe is a glass syringe.

20. The method of claim 3 , wherein the syringe has been terminally sterilized by steam sterilization.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2020
From: GOODING, TAMERA; KENNEDY, STEPHEN J.; SHERWOOD, CHARLES H.
To: ANIKA THERAPEUTICS, INC.
Reel/Frame 054280/0368 →
Continuity (9)
Continuation 16040705 · Jul 20, 2018
Continuation 14807958 · Jul 24, 2015
Continuation 13659376 · Oct 24, 2012
Continuation 13165196 · Jun 21, 2011
Division 11638307 · Dec 13, 2006
Provisional Application 60751414 · Dec 14, 2005
Provisional Application 60751381 · Dec 14, 2005
Provisional Application 60751237 · Dec 14, 2005
Related Publication 20210213043A1 · Jul 15, 2021
Cited By (3)
US 12,390,559 US 12,453,804 US 12,697,419