IP Library Granted Patent US 11,197,845
Granted Patent B2
US 11,197,845 · App. 16/598,029 · Granted Dec 14, 2021

Combinations of cannabinoids and N-acylethanolamines

Inventors: Ephraim Brener (Rishon LeZion, IL); Elran Haber (Kiryat-Ono, IL); Ascher Shmulewitz (Tel Aviv, IL)
Assignee: SciSparc Ltd.
A61K31/352A61K31/164A61K36/185A61K45/06A61P25/00A61P25/14A61P25/30A61P29/00
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Quick Facts
Patent No.
US 11,197,845
App. No.
16/598,029
Granted
Dec 14, 2021
Kind
B2
Abstract

The present invention provides pharmaceutical compositions comprising cannabinoids and N-acylethanolamines, and methods for their use in preventing and treating a variety of cannabinoid-treatable conditions.

Claims (24)

1. A method for preventing or treating at least one side-effect associated with cannabinoid consumption in a human subject in need thereof, comprising

administering to the subject a therapeutically-effective amount of a pharmaceutical composition to prevent or treat the at least one side-effect,

wherein the composition comprises at least one phyto-cannabinoid or a salt thereof, and at least one N-acylethanolamine or a salt thereof,

wherein the at least one phyto-cannabinoid is tetrahydrocannabinol (THC) or a salt thereof, and

wherein the at least one phyto-cannabinoid and the at least one N-acylethanolamine are present in the composition in a molar ratio of about 1:0.2 to about 1:2000.

2. The method of claim 1 , wherein the molar ratio between the at least one phyto-cannabinoid or a salt thereof, and the at least one N-acylethanolamine or a salt thereof is between about 1:0.2 to about 1:5.

3. The method of claim 1 , wherein the molar ratio between the at least one phyto-cannabinoid or a salt thereof, and the at least one N-acylethanolamine or a salt thereof is between about 1:1 to about 1:50.

4. The method of claim 1 , wherein the molar ratio between the at least one phyto-cannabinoid or a salt thereof, and the at least one N-acylethanolamine or a salt thereof is between about 1:15 to about 1:1800.

5. The method of claim 1 , wherein the molar ratio between the at least one phyto-cannabinoid or a salt thereof, and the at least one N-acylethanolamine or a salt thereof is between about 1:25 to about 1:450.

6. The method of claim 1 , wherein the molar ratio between the at least one phyto-cannabinoid or a salt thereof, and the at least one N-acylethanolamine or a salt thereof is between about 1:50 to about 1:100.

7. The method of claim 1 , wherein the pharmaceutical composition comprises about 50-1800 mg of N-acylethanolamine or a salt thereof.

8. The method of claim 7 , wherein the pharmaceutical composition comprises about 50 mg, about 100 mg, about 150 mg, about 200 mg, about 250 mg, about 500 mg, about 750 mg, about 1000 mg or about 1500 mg of N-acylethanolamine or a salt thereof.

9. The method of claim 1 , wherein the at least one N-acylethanolamine is N-palmitoylethanolamine (PEA), Me-palmitoylethanolamide (Me-PEA), palmitoylcyclohexamide, palmitoylbutylamide, palmitoylisopropylamide, oleoylethanolamine (OEA), palmitoylisopropylamide (PIA), a salt thereof, or any combination thereof.

10. The method of claim 9 , wherein the at least one N-acylethanolamine is PEA or a salt thereof.

11. The method of claim 1 , wherein the pharmaceutical composition comprises THC or a salt thereof, and PEA or a salt thereof.

12. The method of claim 1 , wherein the pharmaceutical composition comprises about 0.5-10 mg of THC or a salt thereof, and about 200-1800 mg of PEA or a salt thereof.

13. The method of claim 1 , wherein the pharmaceutical composition comprises about 2.5-10 mg of THC or a salt thereof and about 250-1000 mg of PEA or a salt thereof.

14. The method of claim 1 , wherein the pharmaceutical composition comprises about 2.5 mg, about 5 mg, about 7.5 mg or about 10 mg of THC or a salt thereof, and about 250 mg, about 500 mg, about 750 mg or about 1000 mg of PEA or a salt thereof.

15. The method of claim 1 , wherein the pharmaceutical composition is formulated for oral, oral mucosal, nasal, sublingual, inhalational, topical, rectal, vaginal, parenteral, intravenous, intramuscular, or subcutaneous administration.

16. The method of claim 1 , wherein the at least one phyto-cannabinoid comprises THC or a salt thereof and CBD or a salt thereof in a molar ratio between the THC or a salt thereof and the CBD or a salt thereof between about 2:1 to about 1:2.

17. The method of claim 1 , wherein the administration of the at least one phyto-cannabinoid and the N-acylethanolamine is repeated.

18. The method of claim 1 , wherein the at least one side-effect associated with cannabinoid consumption is increased appetite or body-weight gain.

19. The method of claim 1 , wherein the at least one side-effect associated with cannabinoid consumption is confusion or disorientation.

20. The method of claim 1 , wherein the at least one side-effect associated with cannabinoid consumption is anxiety.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2025
From: SCISPARC LTD.
To: NEUROTHERA LABS INC.
Reel/Frame 073090/0774 →
CHANGE OF NAME Recorded May 5, 2021
From: THERAPIX BIOSCIENCES LTD
To: SCISPARC LTD
Reel/Frame 056151/0744 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2021
From: SHMULEWITZ, ASCHER; HABER, ELRAN; BRENER, EPHRAIM
To: THERAPIX BIOSCIENCES LTD.
Reel/Frame 055909/0325 →
Continuity (3)
Division 15570118
Provisional Application 62154144 · Apr 29, 2015
Related Publication 20200038367A1 · Feb 6, 2020
Cited By (1)
US 12,491,200