Cannabinoid prodrug compounds
US-2024408046-A1 · Dec 12, 2024 · US
US11072579B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11072579-B2 |
| Application number | US-201916359446-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 20, 2019 |
| Priority date | Mar 13, 2013 |
| Publication date | Jul 27, 2021 |
| Grant date | Jul 27, 2021 |
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The present invention relates to a method of treating cataplexy in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of certain carbamate compounds.
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We claim: 1. A method of treating cataplexy in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of Formula (I): or a pharmaceutically acceptable salt or ester thereof; wherein R is a member selected from the group consisting of hydrogen, lower alkyl of 1 to 4 carbon atoms, halogen selected from F, Cl, Br and I, alkoxy containing 1 to 3 carbon atoms, nitro, hydroxy, trifluoromethyl, and thioalkoxy containing 1 to 3 carbon atoms; x is an integer of 0 to 3, with the proviso that R may be the same or different when x is 2 or 3; R 1 and R 2 are independently selected from the group consisting of hydrogen, lower alkyl of 1 to 4 carbon atoms, aryl, arylalkyl, cycloalkyl of 3 to 7 carbon atoms; or R 1 and R 2 can be joined to form a 5 to 7-membered heterocycle substituted with a member selected from the group consisting of hydrogen, alkyl, and aryl groups, wherein the heterocycle can comprise 1 to 2 nitrogen atoms and 0 to 1 oxygen atom, wherein the nitrogen atoms are not directly connected with each other or with the oxygen atom. 2. The method of claim 1 , wherein x=0. 3. The method of claim 1 , wherein the compound of Formula I is an enantiomer of Formula I substantially free of other enantiomers or an enantiomeric mixture wherein one enantiomer of Formula I predominates. 4. The method of claim 3 , wherein the enantiomer of Formula I predominates to the extent of about 98% or greater. 5. The method of claim 1 , wherein the cataplexy is associated with narcolepsy. 6. The method of claim 1 , wherein the cataplexy is secondary to a condition that lowers hypocretin levels in the subject. 7. The method of claim 6 , wherein the condition is selected from the group consisting of brain tumor, astrocytomas, glioblastoma, glioma, subependynoma, craniopharyngioma, arterio-venous malformations, ischemic events, multiple sclerosis, head injury, brain surgery, paraneoplastic syndromes, Neimann-Pick type C disease, and encephalitis. 8. The method of claim 1 , wherein the therapeutically effective amount of the compound of Formula I is from about 0.01 mg/kg/dose to about 150 mg/kg/dose. 9. The method of claim 1 , wherein the therapeutically effective amount of the compound of Formula I is from about 1 mg/day to about 7000 mg/day. 10. The method of claim 1 , wherein the compound of Formula I is administered orally. 11. The method of claim 1 , wherein the compound of Formula I is administered in the form of a capsule or tablet. 12. The method of claim 1 , wherein the compound of Formula I is administered in the form of a capsule at a dose of about 150 mg to about 300 mg without any excipients.
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