IP Library Patent Application 17579541
Patent Application
App. No. 17/579,541

FORMULATIONS OF 19-NOR C3,3-DISUBSTITUTED C21-N-PYRAZOLYL STEROID AND METHODS OF USE THEREOF

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Patent No.
US None
App. No.
17/579,541
Abstract

This invention relates to a 19-nor C3,3-disubstituted C21-pyrazolyl steroid of formula (I) and pharmaceutical compositions thereof. Also disclosed herein are methods of making the pharmaceutical compositions of the 19-nor C3,3-disubstituted C21-pyrazolyl steroid of formula (I) and methods of using the 19-nor C3,3-disubstituted C21-pyrazolyl steroid of formula (I) or crystalline solid forms, pharmaceutically acceptable salts, and pharmaceutically acceptable compositions thereof.

Claims (52)

1 - 142 . (canceled)

143 . A pharmaceutical composition comprising:

(i) about 10% (w/w) to about 15% (w/w) of a crystalline form of the compound of formula (I)

(ii) about 60% (w/w) to about 70% (w/w) of a brittle filler;

(iii) about 10% (w/w) to about 20% (w/w) of a ductile filler;

(iv) about 4% (w/w) to about 8% (w/w) of a disintegrant;

(v) about 0.5% (w/w) to about 2% (w/w) of a glidant; and

(vi) about 1% (w/w) to about 2% (w/w) of a lubricant.

144 . The pharmaceutical composition of claim 143 , wherein the brittle filler comprises mannitol, lactose, sucrose, fructose, glucose, maltose, dibasic calcium phosphate, hydroxyapatite, sodium carbonate, sodium bicarbonate, calcium carbonate, bentonite, kaolin, or a combination thereof.

145 . The pharmaceutical composition of claim 143 , wherein the brittle filler comprises mannitol.

146 . The pharmaceutical composition of claim 143 , wherein the ductile filler comprises a microcrystalline cellulose, a starch, a polysaccharide, a hydroxypropylcellulose, a hypromellose, a carboxymethylcellulose, a methylcellulose, a hydroxypropylmethylcellulose, a polyvinylpyrrolidone, a polyvinyl acrylate, a hydroxypropylcellulose, a hypromellose, a carboxymethylcellulose, a methylcellulose, a hydroxypropylmethylcellulose, or a combination thereof.

147 . The pharmaceutical composition of claim 143 , wherein the ductile filler comprises a microcrystalline cellulose.

148 . The pharmaceutical composition of claim 147 , wherein the microcrystalline cellulose comprises a silicified microcrystalline cellulose.

149 . The pharmaceutical composition of claim 143 , wherein the disintegrant comprises sodium starch glycolate, a crospovidone, croscarmellose sodium, or a combination thereof.

150 . The pharmaceutical composition of claim 143 , wherein the disintegrant comprises croscarmellose sodium.

151 . The pharmaceutical composition of claim 143 , wherein the glidant comprises colloidal silicon dioxide, talc, kaolin, bentonite, or a combination thereof.

152 . The pharmaceutical composition of claim 143 , wherein the glidant comprises colloidal silicon dioxide.

153 . The pharmaceutical composition of claim 143 , wherein the comprises sodium stearyl fumarate, magnesium stearate, stearic acid, glyceryl behenate, or a combination thereof.

154 . The pharmaceutical composition of claim 143 , wherein the comprises sodium stearyl fumarate.

155 . The pharmaceutical composition of claim 143 , wherein the crystalline form of the compound of formula (I) comprises crystalline Form A, wherein crystalline Form A exhibits an X-ray powder diffraction pattern comprising characteristic peaks at the following diffraction angles (2θ): 9.5°±0.2°, 10.8°±0.2°, 13.2°±0.2°, 14.9°±0.2°, 16.0°±0.2°, 18.3°±0.2°, 18.9°±0.2°, 21.1°±0.2°, 21.6°±0.2°, and 23.5°±0.2°.

156 . The pharmaceutical composition of claim 143 , wherein the crystalline form of the compound of formula (I) comprises crystalline Form C, wherein crystalline Form C exhibits an X-ray powder diffraction pattern comprising characteristic peaks at the following diffraction angles (2θ): 9.9°±0.2°, 11.8°±0.2°, 13.4°±0.2°, 14.4°±0.2°, 14.8°±0.2°, 17.0°±0.2°, 20.7°±0.2°, 21.5°±0.2°, and 22.6°±0.2°.

157 . The pharmaceutical composition of claim 143 , wherein the crystalline form of the compound of formula (I) comprises crystalline Form C, wherein crystalline Form C exhibits an X-ray powder diffraction pattern comprising characteristic peaks at the following diffraction angles (2θ): 9.9°±0.2°, 14.8°±0.2°, 17.0°±0.2°, 20.7°±0.2°, and 21.5°±0.2°.

158 . A pharmaceutical composition comprising:

(i) about 20 mg of a crystalline form of the compound of formula (I)

(ii) about 105.9 mg of mannitol;

(iii) about 26.2 mg of silicified microcrystalline cellulose;

(iv) about 10 mg of croscarmellose sodium;

(v) about 1.7 mg of colloidal silicon dioxide; and

(vi) about 2.9 mg of sodium stearyl fumarate.

159 . A pharmaceutical composition comprising:

(i) about 25 mg of a crystalline form of the compound of formula (I)

(ii) about 132 mg of mannitol;

(iii) about 32.7 mg of the silicified microcrystalline cellulose;

(iv) about 12.5 mg of croscarmellose sodium;

(v) about 2.1 mg of colloidal silicon dioxide; and

(vi) about 3.6 mg of sodium stearyl fumarate.

160 . A pharmaceutical composition comprising:

(i) about 30 mg of a crystalline form of the compound of formula (I)

(ii) about 159 mg of mannitol;

(iii) about 39.3 mg of the silicified microcrystalline cellulose;

(iv) about 15 mg of croscarmellose sodium;

(v) about 2.5 mg of colloidal silicon dioxide; and

(vi) about 4.4 mg of sodium stearyl fumarate.

161 . A dosage form intended for oral administration comprising a pharmaceutical composition of claim 143 .

162 . The dosage form of claim 161 , wherein the dosage form is selected from the group consisting of a powder, a sachet, a stickpack, a capsule, a minitab, and a tablet.

163 . The dosage form of claim 161 , wherein the dosage form is a capsule.

164 . The dosage form of claim 163 , wherein the size of the capsule is selected from the group consisting of 000, 00, 0, 1, 2, 3, 4, and 5.

165 . The dosage form of claim 164 , wherein the size of the capsule is 1.

166 . A method of treating a CNS-related disorder, the method comprising administering to a subject in need thereof a pharmaceutical composition of claim 143 .

167 . The method of claim 166 , wherein the CNS-related disorder comprises a sleep disorder, a mood disorder, a schizophrenia spectrum disorder, a convulsive disorder, a disorder of memory and/or cognition, a movement disorder, a personality disorder, autism spectrum disorder, pain, traumatic brain injury, a vascular disease, a substance abuse disorder and/or withdrawal syndrome, tinnitus, or status epilepticus.

168 . A method of treating major depressive disorder, the method comprising administering to a subject in need thereof a pharmaceutical composition of claim 143 .

169 . A method of treating postpartum depression, the method comprising administering to a subject in need thereof a pharmaceutical composition of claim 143 .

Assignments (5)
CHANGE OF NAME Recorded May 13, 2026
From: SAGE THERAPEUTICS, INC.
To: SAGE THERAPEUTICS, LLC
Reel/Frame 075610/0448 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2024
From: WATSON, PAUL STEVEN; BERNER, BRET; NARAYAN, PADMA; CHEN, XIAOXIA
To: SAGE THERAPEUTICS, INC.
Reel/Frame 068067/0519 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 16, 2024
From: WATSON, PAUL STEVEN; BERNER, BRET; NARAYAN, PADMA; CHEN, XIAOXIA
To: SAGE THERAPEUTICS, INC.
Reel/Frame 066477/0814 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 16, 2024
From: STUTZMAN, TODD ANTHONY; MENG, JIANING; WILKERSON, CAROLYN S.; JAIN, RAJ RAMNIK
To: CATALENT PHARMA SOLUTIONS, LLC
Reel/Frame 066478/0287 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 16, 2024
From: CATALENT PHARMA SOLUTIONS, LLC
To: SAGE THERAPEUTICS, INC.
Reel/Frame 066478/0740 →