IP Library Patent Application 16337982
Patent Application
App. No. 16/337,982

CRYSTALLINE FORMS OF A BILE ACID DERIVATIVE

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
16/337,982
Abstract

A crystalline form of a bile acid compound and methods of preparation and use thereof are described.

Claims (31)

1 . A crystalline form of Compound 1-Na, characterized by having X-ray powder diffraction (XRPD) peaks at approximately 8.5, 15.8, and 16.7° 2θ (theta) using Cu Kα radiation.

2 . The crystalline form of claim 1 , characterized by having XRPD peaks at approximately 4.0, 8.5, 15.8, 16.7, 17.8, and 18.2° 2θ (theta) using Cu Kα radiation.

3 . The crystalline form of claim 1 , characterized by having XRPD peaks at approximately 4.0, 6.6, 7.1, 8.5, 11.5, 13.5, 15.8, 16.7, 17.8, and 18.2° 2θ (theta) using Cu Kα radiation.

4 . The crystalline form of claim 1 , characterized by having an XRPD pattern substantially similar to that shown in FIG. 3 , FIG. 7 , FIG. 17 or FIG. 19 .

5 . The crystalline form of claim 1 , further characterized by a Differential Scanning calorimetry (DSC) having an onset temperature between about 165° C. and about 169° C.

6 . The crystalline form of claim 1 , further characterized by a DSC having an onset temperature at approximately 165° C. or 167° C.

7 . The crystalline form of claim 1 , further characterized by a DSC having an onset temperature at about 30° C.

8 . The crystalline form of claim 1 , further characterized by a DSC having an onset temperature at approximately 29° C.

9 . The crystalline form of claim 1 , further characterized by a DSC having a first onset temperature at about 30° C. and a second onset temperature between about 165° C. and about 169° C.

10 . The crystalline form of claim 1 , further characterized by a DSC having a first onset temperature at approximately 29° C. and a second onset temperature at approximately 165° C. or 169° C.

11 . A crystalline form of Compound 1-Na, characterized by having an orthorhombic crystal system with the following unit cell parameters: a=approximately 8.7 Å, b=approximately 27.0 Å, and c=approximately 34.8 Å.

12 . A pharmaceutical composition comprising the crystalline form of any one of claims 1 - 11 , and a pharmaceutically acceptable diluent, excipient or carrier.

13 . A method of treating or preventing an FXR-medated disease or disorder in a subject in need thereof, comprising administering a therapeutically effective amount of the crystalline form of any one of claims 1 - 11 .

14 . A method of modulating FXR in a subject in need thereof, comprising administering a therapeutically effective amount of the crystalline form of any one of claims 1 - 11 .

15 . A method of preparing a crystalline form of Compound 1-Na, comprising:

(a) dissolving amorphous Compound 1-Na in a solvent to form a solution;

(b) cooling the solution;

(c) repeating step (a) and step (b) for one or more times; and

(f) filtering the product from step (c) and drying the product under vacuum.

16 . A method of preparing a crystalline form of Compound 1-Na, comprising:

(a) dissolving amorphous Compound 1-Na in a solvent to form a solution;

(b) optionally cooling the solution comprising Compound 1-Na;

(c) adding a crystalline seed of the crystalline Form A of Compound 1-Na to the solution;

(d) adding acetonitrile to the solution;

(e) cooling the solution; and

(f) isolating the crystalline Form A of Compound 1-Na under vacuum filtration.

17 . A crystalline form of claim 1 , characterized by having X-ray powder diffraction (XRPD) peaks at 8.5±0.2° two theta, 15.8±0.2° two theta, and 16.7±0.2° two theta using Cu Kα radiation.

18 . The crystalline form of claim 1 , characterized by having XRPD peaks at 4.0±0.2° two theta, 8.5±0.2° two theta, 15.8±0.2° two theta, 16.7±0.2° two theta, 17.8±0.2° two theta, and 18.2±0.2° two theta using Cu Kα radiation.

19 . The crystalline form of claim 1 , characterized by having XRPD peaks at 4.0±0.2° two theta, 6.6±0.2° two theta, 7.1±0.2° two theta, 8.5±0.2° two theta, 11.5±0.2° two theta, 13.5±0.2° two theta, 15.8±0.2° two theta, 16.7±0.2° two theta, 17.8±0.2° two theta, and 18.2±0.2° two theta using Cu Kα radiation.

20 . A crystalline form of claim 11 characterized by having an orthorhombic space group P2 1 2 1 2 1 .

21 . A crystalline form of claim 1 characterized by having an orthorhombic space group P2 1 2 1 2 1 .

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Jan 4, 2024
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION
To: INTERCEPT PHARMACEUTICALS, INC.
Reel/Frame 066662/0210 →
CHANGE OF ADDRESS Recorded Aug 22, 2022
From: INTERCEPT PHARMACEUTICALS, INC.
To: INTERCEPT PHARMACEUTICALS, INC.
Reel/Frame 061297/0990 →
SECURITY INTEREST Recorded Aug 18, 2021
From: INTERCEPT PHARMACEUTICALS, INC.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 057650/0772 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 27, 2020
From: STRAZIK, RACHEL P.
To: INTERCEPT PHARMACEUTICALS, INC.
Reel/Frame 054176/0236 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2019
From: EBERLIN, ALEX; ESPINOSA, ROSA M
To: JOHNSON MATTHEY PLC
Reel/Frame 048736/0735 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2019
From: JOHNSON MATTHEY PLC
To: INTERCEPT PHARMACEUTICALS, INC
Reel/Frame 048736/0788 →