Claims for Patent: 12,209,059

Summary for Patent: 12,209,059

Title:	Treatment of sleep-wake disorders
Abstract:	This invention is directed to a method of treating Excessive daytime Sleepiness (EDS) in a subject, comprising the step of administering a therapeutically effective amount of a compound of Formula (I): Formula (I) or a pharmaceutically acceptable salt or ester thereof wherein Rx is a member selected from the group consisting of hydrogen, lower alkyl of 1 to 8 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 1 to 3, with the proviso that R may be the same or different when x is 2 or 3; R1 and R2 can be the same or different from each other and are independently selected from the group consisting of hydrogen, lower alkyl of 1 to 8 carbon atoms, aryl, arylalkyl, cycloalkyl of 3 to 7 carbon atoms; R1 and R2 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 cyclic compound 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 ox en atom.
Inventor(s):	Abdallah Ahnaou, Wilhelmus H.I.M. Drinkenburg, Joseph Palumbo, Jonathan Sporn
Assignee:	SK Biopharmaceuticals Co Ltd
Application Number:	US18/364,689
Patent Claims:	1. A method of treating Excessive Daytime Sleepiness (EDS) in a subject, comprising administration, to a subject in need of such treatment, of a therapeutically effective amount of a compound of the 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 8 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 1 to 3, with the proviso that R may be the same or different when x is 2 or 3; R1 and R2 can be the same or different from each other and are independently selected from the group consisting of hydrogen, lower alkyl of 1 to 8 carbon atoms, aryl, arylalkyl, cycloalkyl of 3 to 7 carbon atoms; or R1 and R2 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 cyclic compound 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; and further wherein the administration comprises a once daily oral tablet. 2. The method of claim 1 wherein R is hydrogen and x=1. 3. The method of claim 1 wherein R, R1 and R2 are all selected from hydrogen and x=1. 4. A method of treating Excessive Daytime Sleepiness (EDS) in a subject, comprising the step of administration, to a subject in need of such treatment, of a therapeutically effective amount of an enantiomer of Formula I substantially free of other enantiomers or an enantiomeric mixture wherein one enantiomer of Formula I predominates; 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 8 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 1 to 3, with the proviso that R may be the same or different when x is 2 or 3; R1 and R2 can be the same or different from each other and are independently selected from the group consisting of hydrogen, lower alkyl of 1 to 8 carbon atoms, aryl, arylalkyl, cycloalkyl of 3 to 7 carbon atoms; or R1 and R2 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 cyclic compound 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; and further wherein the administration comprises a once daily oral tablet. 5. The method of claim 4 wherein Rx is hydrogen and x=1. 6. The method of claim 4 wherein Rx, R1 and R2 are all selected from hydrogen and x=1. 7. The method of claim 4 wherein one enantiomer predominates to the extent of about 90% or greater. 8. The method of claim 4 wherein one enantiomer predominates to the extent of about 98% or greater. 9. The method of claim 4 wherein the enantiomer of Formula I is an enantiomer of Formula Ia or a pharmaceutically acceptable salt or ester thereof. 10. The method of claim 9 wherein the enantiomer of Formula Ia is the (R) or (D) enantiomer. 11. The method of claim 9 wherein the enantiomer of Formula Ia is the(S) or (L) enantiomer. 12. The method of claim 9 wherein one enantiomer predominates to the extent of about 90% or greater. 13. The method of claim 9 wherein one enantiomer predominates to the extent of about 98% or greater. 14. The method of claim 4 wherein the enantiomer of Formula I substantially free of other enantiomers is (R)-(beta-amino-benzenepropyl) carbamate or an enantiomeric mixture wherein (R)-(beta-amino-benzenepropyl) carbamate predominates. 15. The method of claim 14 wherein (R)-(beta-amino-benzenepropyl) carbamate predominates to the extent of about 90% or greater. 16. The method of claim 14 wherein (R)-(beta-amino-benzenepropyl) carbamate predominates to the extent of about 98% or greater. 17. The method of claim 14 wherein the cause of the EDS is chosen from the group consisting of central nervous system (CNS) pathologic abnormalities, stroke, narcolepsy, idiopathic CNS hypersomnia, sleep deficiency, sleep apnea, obstructive sleep apnea, insufficient nocturnal sleep, chronic pain, acute pain, Parkinson's disease, urinary incontinence, multiple sclerosis fatigue, Attention Deficit Hyperactivity Disorder (ADHD), Alzheimer's disorder, Major Depression, Bipolar Disorder, cardiac ischemia, misalignments of the body's circadian pacemaker with the environment, jet lag, shift work, and sedating drugs. 18. The method of claim 14 wherein the cause of the EDS is narcolepsy. 19. The method of claim 14 wherein the once daily oral tablet of (R)-(beta-amino-benzenepropyl) carbamate is in a dose range from about 0.1 mg/day to about 1000 mg/day.