IP Library Granted Patent US 11,471,456
Granted Patent B2
US 11,471,456 · App. 16/789,342 · Granted Oct 18, 2022

Formulations comprising heterocyclic protein kinase inhibitors

Inventors: Steven L. Warner (Sandy, UT); Adam Siddiqui-Jain (South Jordan, UT); Paul Flynn (Citrus Heights, CA)
Assignee: Sumitomo Pharma Oncology, Inc.
A61K31/5025A61K9/4816A61K31/25A61K31/519A61P35/00C07D487/04C07B2200/13
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Quick Facts
Patent No.
US 11,471,456
App. No.
16/789,342
Granted
Oct 18, 2022
Kind
B2
Abstract

Provided is a composition comprising a polyglycolized glyceride and a compound having the following structure (I): or a pharmaceutically acceptable salt thereof. Also provided are crystalline forms of the compound of structure (I), or a pharmaceutically acceptable salt thereof. Methods of making the same, and methods for using the same in the treatment of cancer, autoimmune, inflammatory and other Pim kinase-associated diseases, disorders or conditions are also disclosed.

Claims (30)

1. A crystalline form of the hydrochloric acid salt of a compound having the following structure (I):

characterized by an X-ray powder diffraction pattern comprising peaks, in terms of 2-theta, at 21.5±0.2°, 19.9±0.2°, and 17.8±0.2°.

2. The crystalline form of claim 1 , further characterized by an X-ray powder diffraction pattern comprising a peak, in terms of 2-theta, at 19.3±0.2°.

3. The crystalline form of claim 2 , further characterized by an X-ray powder diffraction pattern comprising a peak, in terms of 2-theta, at 24.4±0.2°.

4. The crystalline form of claim 3 , further characterized by an X-ray powder diffraction pattern comprising a peak, in terms of 2-theta, at 16.3±0.2°.

5. The crystalline form of claim 1 , characterized by an X-ray powder diffraction pattern comprising at least three peaks at 2-theta angles selected from the group consisting of 24.4±0.2°, 21.5±0.2°, 19.9±0.2°, 19.3±0.2°, 17.8±0.2° and 16.3±0.2°.

6. The crystalline form of claim 5 , further characterized by an X-ray powder diffraction pattern substantially lacking a peak, in terms of 2-theta, at 15.7±0.2°.

7. The crystalline form of claim 6 , further characterized by an X-ray powder diffraction pattern substantially lacking a peak, in terms of 2-theta, at 17.0±0.2°.

8. The crystalline form of claim 7 , further characterized by an X-ray powder diffraction pattern substantially lacking a peak, in terms of 2-theta, at 19.0±0.2°.

9. The crystalline form of claim 1 , which is Form I having an X-ray powder diffraction pattern substantially in accordance with that shown in FIG. 1 .

10. The crystalline form of claim 1 , which is Form I having a differential scanning calorimetry thermogram substantially in accordance with that shown in FIG. 2 .

11. The crystalline form of claim 1 , which is Form I having a thermogravimetric analysis diagram substantially in accordance with that shown in FIG. 3 .

12. The crystalline form of claim 1 , which is Form I having a melting temperature of 226±3° C.

13. The crystalline form of claim 1 , wherein the crystalline form is substantially pure.

14. A composition comprising the crystalline form of 1 , and a pharmaceutically acceptable carrier.

15. A composition comprising:

a polyglycolized glyceride; and

a compound having the following structure (I):

or a pharmaceutically acceptable salt thereof.

16. The composition of claim 15 , wherein the polyglycolized glyceride has a melting point ranging from about 30° C. to about 50° C.

17. The composition of claim 15 , wherein the polyglycolized glyceride has a hydrophile/lipophile balance (HLB) value ranging from about 8 to about 18.

18. The composition of claim 15 , wherein the polyglycolized glyceride comprises lauroyl polyoxy-32 glycerides.

19. The composition of claim 15 , wherein the composition comprises the compound of structure (I), or a pharmaceutically acceptable salt thereof, in a concentration ranging from about 10 weight percent (wt %) to about 40 wt %, as determined using the molecular weight of the compound of structure (I) as a hydrochloride salt.

20. The composition of claim 15 , wherein the composition comprises the polyglycolized glyceride in a concentration ranging from about 50 wt % to about 90 wt %.

21. The composition of claim 15 , wherein the composition comprises the compound of structure (I), or a pharmaceutically acceptable salt thereof, and the polyglycolized glyceride at a weight ratio ranging from about 1:1 to about 1:10, as determined using the molecular weight of the compound of structure (I) as a free base.

22. A unit dose form comprising the composition of claim 15 in a therapeutically effective amount.

23. A unit dose form comprising a composition, the composition comprising:

a polyglycolized glyceride in an amount of about 560 mg to about 600 mg; and

a compound having the following structure (I):

or a pharmaceutically acceptable salt thereof, in an amount of about 115 mg to about 125 mg, as determined using the molecular weight of the compound of structure (I) as a free base.

Assignments (5)
MERGER Recorded Sep 18, 2024
From: SUMITOMO PHARMA ONCOLOGY, INC.
To: SUMITOMO PHARMA AMERICA, INC.
Reel/Frame 068618/0375 →
CHANGE OF NAME Recorded Apr 25, 2022
From: SUMITOMO DAINIPPON PHARMA ONCOLOGY, INC.
To: SUMITOMO PHARMA ONCOLOGY, INC.
Reel/Frame 059787/0758 →
MERGER Recorded Jul 10, 2020
From: TOLERO PHARMACEUTICALS, INC.
To: BOSTON BIOMEDICAL, INC.
Reel/Frame 053172/0940 →
CHANGE OF NAME Recorded Jul 10, 2020
From: BOSTON BIOMEDICAL, INC.
To: SUMITOMO DAINIPPON PHARMA ONCOLOGY, INC.
Reel/Frame 053184/0718 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2020
From: WARNER, STEVEN L.; SIDDIQUI-JAIN, ADAM; FLYNN, PAUL
To: TOLERO PHARMACEUTICALS, INC.
Reel/Frame 052035/0192 →