Claims for Patent: 10,188,652

Summary for Patent: 10,188,652

Title:	Compositions and methods for treating insomnia
Abstract:	In the present invention, compound such as (1R,2S)-2-(((2,4-dimethylpyrimidin-5-yl)oxy)methyl)-2-(3-fluorophenyl)-N-- (5-fluoropyridin-2-yl) cyclopropanecarboxamide have been found to be potent orexin receptor antagonists, and may be useful in the treatment of sleep disorders such as insomnia, as well as for other therapeutic uses.
Inventor(s):	Moline; Margaret (Woodcliff Lake, NJ), Pastino; Gina (Woodcliff Lake, NJ), Akimoto; Yurie (Kakamigahara, JP), Zaima; Yasuhiro (Kakamigahara, JP), Suzuki; Nobuya (Kakamigahara, JP), Yoshida; Nobuo (Kakamigahara, JP)
Assignee:	Eisai R&D Management Co., Ltd. (Tokyo, JP)
Application Number:	15/519,676
Patent Claims:	1. A method of treating insomnia, comprising administrating orally a dosage form comprising a therapeutically effective amount of compound A, wherein said therapeutically effective amount is a single daily dose ranging from about 2.5 mg to about 10 mg, wherein said single daily dose achieves a mean Cmax of from about 3.0 ng/ml to about 7.2 ng/ml for each 1 mg of compound A after administration to human subjects, and said compound A is (1R,2S)-2-(((2,4-dimethylpyrimidin-5-yl)oxy)methyl)-2-(3-fluorophenyl)-N-- (5-fluoropyridin-2-yl) cyclopropanecarboxamide represented by the following formula: ##STR00002## 2. The method of claim 1, wherein said therapeutically effective amount is a single 5 mg daily dose, wherein said single 5 mg daily dose achieves a mean Cmax within the range of about 80% to about 125% of 23 ng/ml. 3. The method of claim 1, wherein said therapeutically effective amount is a single 10 mg daily dose, wherein said single 10 mg daily dose achieves a mean Cmax within the range of about 80% to about 125% of 36 ng/ml. 4. The method of claim 1, wherein said therapeutically effective amount is a single daily dose to achieve a mean AUC(0-24) of from about 15.9 ng*hr/ml to about 23.8 ng*hr/ml for each 1 mg of compound A. 5. The method of claim 1, wherein said therapeutically effective amount is a single 5 mg daily dose, wherein said single 5 mg daily dose achieves a mean AUC(0-24) within the range of about 80% to about 125% of 95 ng*hr/ml. 6. The method of claim 1, wherein said therapeutically effective amount is a single 10 mg daily dose, wherein said single 10 mg daily dose achieves a mean AUC(0-24) within the range of about 80% to about 125% of 159 ng*hr/ml. 7. The method of claim 1, wherein said therapeutically effective amount is a single daily dose to achieve a mean AUC(0-t) of from about 19.1 ng*hr/ml to about 51.1 ng*hr/ml for each 1 mg of compound A. 8. The method of claim 1, wherein said therapeutically effective amount is a single 5 mg daily dose, wherein said single 5 mg daily dose achieves a mean AUC(0-t) within the range of about 80% to about 125% of 128 ng*hr/ml. 9. The method of claim 1, wherein said therapeutically effective amount is a single 10 mg daily dose, wherein said single 10 mg daily dose achieves a mean AUC(0-t) within the range of about 80% to about 125% of 284 ng*hr/ml. 10. The method of claim 1, wherein said therapeutically effective amount is a single daily dose to achieve a mean AUC(0-inf) of from about 19.8 ng*hr/ml to about 53.1 ng*hr/ml for each 1 mg of compound A. 11. The method of claim 1, wherein said therapeutically effective amount is a single 5 mg daily dose, and wherein said single 5 mg daily dose achieves a mean AUC(0-inf) within the range of about 80% to about 125% of 149 ng*hr/ml. 12. The method of claim 1, wherein said therapeutically effective amount is a single 10 mg daily dose, wherein said single 10 mg daily dose achieves a mean AUC(0-inf) within the range of about 80% to about 125% of 311 ng*hr/ml. 13. The method of claim 1, wherein said single daily dose provides a mean plasma compound A concentration of about 20 ng/ml or less at from 8 to 10 hours after single dose administration to human subjects. 14. An oral dosage form comprising a therapeutically effective amount of compound A, lactose and low-substituted hydroxypropyl cellulose, wherein said therapeutically effective amount is a single daily dose ranging from about 2.5 mg to about 10 mg; wherein said dosage form provides a dissolution rate of 85% or more in dissolution medium (0.1 mol/L hydrochloric acid containing 0.5% polysorbate 80, 900 mL, 37.+-.0.5.degree. C.) within 30 minutes from the onset of dissolution study using the Apparatus 2 (Paddle Apparatus, paddle speed; 75 rpm) according to the procedure for immediate-release dosage form in 6.10 Dissolution test of JP16 or <711> Dissolution of USP37; and wherein said compound A is (1R,2S)-2-(((2,4-dimethylpyrimidin-5-yl)oxy)methyl)-2-(3-fluorophenyl)-N-- (5-fluoropyridin-2-yl)cyclopropanecarboxamide represented by the following formula: ##STR00003## 15. The dosage form of claim 14, wherein said dosage form provides a dissolution rate of 85% or more in dissolution medium (0.1 mol/L hydrochloric acid, 900 mL, 37.+-.0.5.degree. C.) within 15 minutes from the onset of dissolution study using the Apparatus 2 (Paddle Apparatus, paddle speed; 50 rpm) according to the procedure for immediate-release dosage form in 6.10 Dissolution test of JP16 or <711> Dissolution of USP37.