IP Library Granted Patent US 9,820,964
Granted Patent B2
US 9,820,964 · App. 15/347,104 · Granted Nov 21, 2017

Ultrapure tetrahydrocannabinol-11-oic acids

Inventor: Mark Tepper (Norwood, MA)
Assignee: Corbus Pharmaceuticals, Inc.
A61K31/352A61K9/007A61K9/0014A61K9/0019A61K9/0048A61K9/0053
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Quick Facts
Patent No.
US 9,820,964
App. No.
15/347,104
Granted
Nov 21, 2017
Kind
B2
Abstract

This application is in the field of medicinal chemistry and relates to ultrapure ajulemic acid, its synthesis, pharmaceutical compositions and methods of use thereof for the treatment and/or prevention of inflammation, pain, and fibrotic diseases including scleroderma, systemic sclerosis, scleroderma-like disorders, sine scleroderma, liver cirrhosis, interstitial pulmonary fibrosis, idiopathic pulmonary fibrosis, Dupuytren's contracture, keloids, chronic kidney disease, chronic graft rejection, and other scarring-wound healing abnormalities, post-operative adhesions, and reactive fibrosis.

Claims (21)

1. A method of treating a subject having a fibrotic disease the method comprising administering to the subject a pharmaceutical composition comprising one or more cannabinoids, wherein said one or more cannabinoids comprise at least 98% (w/w) (6aR,10aR)-3-(1′,1′-dimethylheptyl)-Δ8-tetrahydro-cannabinol-9-carboxylic acid (Ajulemic Acid), or a pharmaceutically acceptable salt thereof, and wherein no significant antinociception is observed in a hot plate test of mice following oral administration to the mice of 10 mg kg of said one or more cannabinoids.

2. The method of claim 1 , wherein said fibrotic disease is selected from the group consisting of scleroderma, liver cirrhosis, interstitial pulmonary fibrosis, idiopathic pulmonary fibrosis, Dupuytren's contracture, keloids, cystic fibrosis, chronic kidney disease, chronic graft rejection, scarring or wound healing abnormalities, post-operative adhesions, reactive fibrosis, dermal fibrosis, lung fibrosis, liver fibrosis, kidney fibrosis, and heart fibrosis.

3. The method of claim 1 , wherein said fibrotic disease is any organ fibrosis.

4. The method of claim 2 , wherein said fibrotic disease is dermal fibrosis.

5. The method of claim 2 , wherein said fibrotic disease is lung fibrosis.

6. The method of claim 2 , wherein said fibrotic disease is scleroderma.

7. The method of claim 2 , wherein the fibrotic disease is cystic fibrosis.

8. The method of claim 2 , wherein said fibrotic disease is idiopathic pulmonary fibrosis.

9. The method of claim 1 , wherein said pharmaceutical composition is administered orally, intravenously, topically, interstitially, by inhalation, via an implant, via a patch, or by ophthalmic administration.

10. The method of claim 9 , wherein said pharmaceutical composition is administered orally.

11. The method of claim 9 , wherein said pharmaceutical composition is administered topically.

12. The method of claim 9 , wherein said pharmaceutical composition is administered intravenously.

13. The method of claim 9 , wherein said pharmaceutical composition is administered by inhalation.

14. The method of claim 1 , wherein said pharmaceutical composition is administered in combination with one or more compounds.

15. The method of claim 1 , wherein said subject is a human.

16. The method of claim 1 , wherein said subject is non-human animal.

17. The method of claim 16 , wherein said non-human animal is a dog or a cat.

18. The method of claim 1 , wherein said pharmaceutical composition is a unit dosage formulation comprising about 0.5 mg to about 120 mg of said (6aR,10aR)-3-(1′,1′-dimethylheptyl)-Δ8-tetrahydro-cannabinol-9-carboxylic acid, or a pharmaceutically acceptable salt thereof, and wherein said unit dosage formulation is administered once daily.

19. The method of claim 1 , wherein said pharmaceutical composition is a unit dosage formulation comprising about 0.15 mg to about 40 mg of said (6aR,10aR)-3-(1′,1′-dimethylheptyl)-Δ8-tetrahydro-cannabinol-9-carboxylic acid, or a pharmaceutically acceptable salt thereof, and wherein said unit dosage formulation is administered up to three times daily.

20. The method of claim 1 , wherein said one or more cannabinoids comprise less than 0.1% (w/w) 11-hydroxy-(6aR,10aR)-3-(1′,1′-dimethylheptyl)-Δ8-tetrahydro-cannabinol (HU-210).

21. The method of claim 2 , wherein said fibrotic disease is systemic sclerosis, sine scleroderma, or a scleroderma-like disorder.

Assignments (6)
SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT SUPPLEMENT Recorded Jun 2, 2025
From: CURIA GLOBAL, INC.; CURIA IP HOLDINGS, LLC; CURIA BIO, INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 071490/0782 →
CHANGE OF NAME Recorded May 20, 2025
From: ALBANY MOLECULAR RESEARCH, INC.
To: CURIA GLOBAL, INC.
Reel/Frame 071298/0097 →
SECURITY INTEREST Recorded Mar 7, 2025
From: CURIA GLOBAL, INC.; CURIA IP HOLDINGS, LLC; CURIA BIO, INC.
To: APOLLO ADMINISTRATIVE AGENCY LLC
Reel/Frame 070442/0908 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2018
From: FREY, DEAN A.; GOEDDEL, DAVID; REINEKE, KARL E.
To: ALBANY MOLECULAR RESEARCH, INC.
Reel/Frame 046713/0858 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2018
From: ALBANY MOLECULAR RESEARCH, INC.
To: CORBUS PHARMACEUTICALS, INC.
Reel/Frame 046713/0955 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2017
From: TEPPER, MARK
To: CORBUS PHARMACEUTICALS, INC.
Reel/Frame 042133/0908 →
Continuity (5)
Division 14546116 · Nov 18, 2014
Continuation PCTUS2014016050 · Feb 12, 2014
Provisional Application 61837743 · Jun 21, 2013
Provisional Application 61763630 · Feb 12, 2013
Related Publication 20170071900A1 · Mar 16, 2017