IP Library Granted Patent US 11,925,626
Granted Patent B2
US 11,925,626 · App. 17/950,902 · Granted Mar 12, 2024

Pharmaceutical formulations containing relacorilant, a heteroaryl-ketone fused azadecalin compound

Inventors: Ian Scott (Dublin, CA); Travis Lemons (Palo Alto, CA); Yip-Fong Chia (Sunnyvale, CA)
Assignee: Corcept Therapeutics Incorporated
A61K31/437A61K9/0053A61K9/4808A61K9/4866A61K47/10A61K47/14A61K47/26
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Quick Facts
Patent No.
US 11,925,626
App. No.
17/950,902
Granted
Mar 12, 2024
Kind
B2
Abstract

Disclosed herein are novel formulations containing relacorilant ((R)-(1-(4-fluorophenyl)-6-(1-methyl-1H-pyrazol-4-yl)sulfonyl)-4,4a,5,6,7,8-hexahydro-1H-pyrazolo[3,4-g]isoquinolin-4a-yl)(4-(trifluoromethyl)pyridin-2-yl)methanone) that are suitable for administration, including oral administration, to patients suffering from disorders amenable to treatment by glucocorticoid receptor modulators (GRMs). Single unit dosage forms comprise softgel capsules containing these formulations. Such softgel capsules may contain, e.g., relacorilant formulations containing 25 milligrams (mg), 50 mg, 100 mg, 200 mg, 300 mg, 400 mg, 500 mg, or other amounts of relacorilant. These novel formulations and single unit dosage forms may be used to treat diseases and disorders including Cushing's syndrome, Cushing's Disease, and other disorders.

Claims (26)

1. A formulation for oral administration of relacorilant, (R)-(1-(4-fluorophenyl)-6-((1-methyl-1H-pyrazol-4-yl)sulfonyl)-4,4a,5,6,7,8-hexahydro-1H-pyrazolo[3,4-g]isoquinolin-4a-yl)(4-(trifluoromethyl)pyridin-2-yl)methanone, which has the following structure:

the formulation comprising:

about 18 to 22% relacorilant;

about 56% to 64% surfactant, wherein said surfactant is lauroyl polyoxyl glyceride, and

about 18% to 22% solubilizer, wherein said solubilizer is propylene glycol monocaprylate,

wherein said percentages are weight percent.

2. The formulation of claim 1 , further including the antioxidant selected from butylated hydroxytoluene (BHT).

3. The formulation of claim 2 , wherein the formulation comprises about 0.02% antioxidant by weight of the formulation.

4. The formulation of claim 2 , consisting of 20% relacorilant, 59.98% surfactant, 20% solubilizer, and 0.02% antioxidant.

5. The formulation of claim 4 , consisting of 25 mg relacorilant, 74.975 mg surfactant, 25 mg solubilizer, and 0.025 mg antioxidant.

6. The formulation of claim 4 , consisting of 50 mg relacorilant, 149.95 mg surfactant, 50 mg solubilizer, and 0.05 mg antioxidant.

7. The formulation of claim 4 , consisting of 100 mg relacorilant, 299.9 mg surfactant, 100 mg solubilizer, and 0.1 mg antioxidant.

8. The formulation of claim 4 , consisting of 150 mg relacorilant, 349.85 mg surfactant, 150 mg solubilizer, and 0.15 mg antioxidant.

9. The formulation of claim 4 , consisting of 200 mg relacorilant, 599.8 mg surfactant, 200 mg solubilizer, and 0.2 mg antioxidant.

10. The formulation of claim 4 , consisting of 300 mg relacorilant, 899.7 mg surfactant, 300 mg solubilizer, and 0.3 mg antioxidant.

11. The formulation of claim 4 , consisting of 400 mg relacorilant, 1199.6 mg surfactant, 400 mg solibilizer, and 0.4 mg antioxidant.

12. The formulation of claim 4 , consisting of 500 mg relacorilant, 1499.5 mg surfactant, 500 mg solubilizer, and 0.5 mg antioxidant.

13. consisting essentially of a softgel capsule containing a relacorilant formulation consisting of 20% relacorilant, 59 .98% surfactant, wherein said surfactant is lauroyl polyoxyl glyceride, and 20% solubilizer, wherein said solubilizer is propylene glycol monocaprylate, and 0.02% antioxidant, wherein said antioxidant is butylated hydroxytoluene (BHT), wherein said percentages are weight percentages.

14. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 25 mg relacorilant, 74.975 mg surfactant, 25 mg solubilizer, and 0.025 mg antioxidant.

15. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 50 mg relacorilant, 149.95 mg surfactant, 50 mg solubilizer, and 0.05 mg antioxidant.

16. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 100 mg relacorilant, 299.9 mg surfactant, 100 mg solubilizer, and 0.1 mg antioxidant.

17. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 150 mg relacorilant, 349.85 mg surfactant, 150 mg solubilizer, and 0.15 mg antioxidant.

18. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 200 mg relacorilant, 599.8 mg surfactant, 200 mg solubilizer, and 0.2 mg antioxidant.

19. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 300 mg relacorilant, 899.7 mg surfactant, 300 mg solubilizer, and 0.3 mg antioxidant.

20. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 400 mg relacorilant, 1199.6 mg surfactant, 400 mg solubilizer, and 0.4 mg antioxidant.

21. The unit dose for oral administration of relacorilant of claim 13 , said softgel capsule containing a relacorilant formulation consisting of 500 mg relacorilant, 1499.5 mg surfactant, 500 mg solubilizer, and 0.5 mg antioxidant.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2022
From: SCOTT, IAN; LEMONS, TRAVIS; CHIA, YIP-FONG
To: CORCEPT THERAPEUTICS INCORPORATED
Reel/Frame 062181/0727 →
Continuity (3)
Continuation 16719644 · Dec 18, 2019
Provisional Application 62781983 · Dec 19, 2018
Related Publication 20230032377A1 · Feb 2, 2023
Cited By (4)
US 12,226,412 US 12,514,849 US 12,589,094 US 12,616,685