IP Library Patent Application 17525046
Patent Application
App. No. 17/525,046

COMBINATIONS OF CANNABINOIDS AND N-ACYLETHANOLAMINES

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 None
App. No.
17/525,046
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 (23)

1 - 48 . (canceled)

49 . A method for preventing or treating pain in a human subject in need thereof, comprising

administering to the subject a pharmaceutical composition in a therapeutically-effective amount to prevent or treat the pain,

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 or salt thereof and the at least one N-acylethanolamine or salt thereof are present in the composition in a molar ratio of about 1:0.2 to about 1:2000, and

wherein the at least one phyto-cannabinoid is tetrahydrocannabinolic acid (THCA), cannabidiol (CBD), cannabinol (CBN), cannabigerol (CBG), cannabichromene (CBC), cannabicyclol (CBL), cannabivarin (CBV), tetrahydrocannabivarin (THCV), cannabidivarin (CBDV), cannabichromevarin (CBCV), cannabigerovarin (CBGV), cannabigerol monomethyl ether (CBGM), a salt thereof, or any combination thereof.

50 . The method of claim 49 , wherein the molar ratio between the at least one phyto-cannabinoid or salt thereof, and the at least one N-acylethanolamine or salt thereof is between about 1:0.2 to about 1:5.

51 . The method of claim 49 , wherein the molar ratio between the at least one phyto-cannabinoid or salt thereof, and the at least one N-acylethanolamine or salt thereof is between about 1:0.5 to about 1:2.

52 . The method of claim 49 , wherein the molar ratio between the at least one phyto-cannabinoid or salt thereof, and the at least one N-acylethanolamine or salt thereof is between about 1:15 to about 1:1800.

53 . The method of claim 49 , wherein the molar ratio between the at least one phyto-cannabinoid or salt thereof, and the at least one N-acylethanolamine or salt thereof is between about 1:25 to about 1:450.

54 . The method of claim 49 , wherein the molar ratio between the at least one phyto-cannabinoid or salt thereof, and the at least one N-acylethanolamine or salt thereof is between about 1:50 to about 1:100.

55 . The method of claim 49 , wherein the at least one phyto-cannabinoid is CBD or a salt thereof.

56 . The method of claim 49 , wherein the pharmaceutical composition comprises about 200-1800 mg of N-acylethanolamine or salt thereof.

57 . The method of claim 56 , wherein the pharmaceutical composition comprises about 250 mg, about 500 mg, about 750 mg, about 1000 mg or about 1500 mg of N-acylethanolamine or salt thereof.

58 . The method of claim 49 , 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.

59 . The method of claim 58 , wherein the at least one N-acylethanolamine is PEA or a salt thereof.

60 . The method of claim 49 , wherein the pharmaceutical composition comprises CBD or a salt thereof, and PEA or a salt thereof.

61 . The method of claim 49 , wherein the pharmaceutical composition comprises about 0.5-10 mg of the phyto-cannabinoid or salt thereof, and about 200-1800 mg of PEA or a salt thereof.

62 . The method of claim 49 , wherein the pharmaceutical composition comprises about 2.5-10 mg of the phyto-cannabinoid or salt thereof and about 250-1000 mg of PEA or a salt thereof.

63 . The method of claim 49 , wherein the pharmaceutical composition comprises about 2.5 mg, about 5 mg, about 7.5 mg or about 10 mg of the phyto-cannabinoid or salt thereof, and about 250 mg, about 500 mg, about 750 mg or about 1000 mg of PEA or a salt thereof.

64 . The method of claim 49 , wherein the pharmaceutical composition is formulated for oral, oral mucosal, nasal, sublingual, inhalational, topical, rectal, vaginal, parenteral, intravenous, intramuscular, or subcutaneous administration.

65 . The method of claim 49 , wherein the administration of the at least one phyto-cannabinoid and the N-acylethanolamine is repeated.

66 . The method of claim 49 , wherein the pain is an acute pain, chronic pain, or neuropathic pain.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2025
From: SCISPARC LTD.
To: NEUROTHERA LABS INC.
Reel/Frame 073090/0774 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2024
From: SHMULEWITZ, ASCHER; HABER, ELRAN; BRENER, EPHRAIM
To: THERAPIX BIOSCIENCES LTD.
Reel/Frame 067680/0977 →
CHANGE OF NAME Recorded Jun 10, 2024
From: THERAPIX BIOSCIENCES LTD
To: SCISPARC LTD
Reel/Frame 067680/0990 →