IP Library Granted Patent US 11,160,811
Granted Patent B2
US 11,160,811 · App. 16/059,439 · Granted Nov 2, 2021

Solid dosage formulations of an orexin receptor antagonist

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Quick Facts
Patent No.
US 11,160,811
App. No.
16/059,439
Granted
Nov 2, 2021
Kind
B2
Abstract

The present invention is directed to a pharmaceutical composition comprising the compound suvorexant, or a pharmaceutically acceptable salt thereof, a concentration-enhancing polymer, and optionally a pharmaceutically acceptable surfactant.

Claims (23)

1. A pharmaceutical composition comprising:

suvorexant in an amorphous form;

hydroxypropyl methyl cellulose acetate succinate;

lactose monohydrate;

croscarmellose sodium;

colloidal silicon dioxide; and

magnesium stearate;

wherein the pharmaceutical composition is prepared by a process comprising spray drying of a mixture comprising suvorexant and hydroxypropyl methyl cellulose acetate succinate, and which comprises 5 mg, 10 mg, 15 mg or 20 mg of suvorexant, and wherein the suvorexant is present in a form that contains at least 90 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

2. The pharmaceutical composition of claim 1 , wherein the suvorexant is present in a form that contains at least 95 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

3. The pharmaceutical composition of claim 1 , wherein the suvorexant is present in a form that contains at least 98 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

4. The pharmaceutical composition of claim 1 , wherein the suvorexant is present in a form that contains at least 99 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

5. A pharmaceutical composition comprising:

suvorexant in an amorphous form;

a concentration-enhancing polymer selected from the group consisting of hydroxypropyl cellulose (HPC), hydroxypropyl methyl cellulose acetate succinate (HPMCAS), hydroxypropyl methylcellulose (HPMC), hydroxypropyl methyl cellulose phthalate (HPMCP), cellulose acetate phthalate (CAP), cellulose acetate trimellitate (CAT), and polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer;

wherein the pharmaceutical composition is prepared by a process comprising spray drying of a mixture comprising suvorexant and the concentration enhancing polymer and which comprises between about 5 mg and about 20 mg of suvorexant, and

wherein the suvorexant is present in a form that contains at least 90 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

6. The pharmaceutical composition of claim 5 , wherein the suvorexant is present in a form that contains at least 95 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

7. The pharmaceutical composition of claim 5 , wherein the suvorexant is present in a form that contains at least 98 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

8. The pharmaceutical composition of claim 5 , wherein the suvorexant is present in a form that contains at least 99 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

9. The pharmaceutical composition of claim 5 , which additionally comprises one or more excipients selected from the group consisting of: croscarmellose sodium, sodium starch glycolate, crospovidone, starch, silicon dioxide, talc, magnesium stearate, stearic acid, sodium stearyl fumarate, microcrystalline cellulose, lactose and mannitol.

10. The pharmaceutical composition of claim 9 , wherein the suvorexant is present in a form that contains at least 95 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

11. The pharmaceutical composition of claim 9 , wherein the suvorexant is present in a form that contains at least 98 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

12. The pharmaceutical composition of claim 9 , wherein the suvorexant is present in a form that contains at least 99 weight % of the amorphous form of suvorexant relative to other morphological forms of suvorexant.

Assignments (2)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2021
From: PAUL A. HARMON; VARIANKAVAL, NARAYAN
To: MERCK SHARP & DOHME
Reel/Frame 057050/0448 →