IP Library Granted Patent US 11,891,372
Granted Patent B2
US 11,891,372 · App. 17/494,923 · Granted Feb 6, 2024

Crystalline forms of 1-((2R,4R)-2-(1H-benzo[d]imidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea maleate

Inventor: Christopher Scott Seadeek (West Lafayette, IN)
Assignee: Pfizer Inc.
C07D401/04A61K31/4439C07B2200/13
View Patent ↗
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 11,891,372
App. No.
17/494,923
Granted
Feb 6, 2024
Kind
B2
Abstract

This invention relates to a crystalline form of 1-((2R,4R)-2-(1H-benzo[d]imidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea maleate, and to pharmaceutical compositions thereof, to intermediates and methods for the production and isolation of such crystalline forms and compositions, and to methods of using such crystalline forms and compositions in the treatment of abnormal cell growth in mammals, especially humans.

Claims (44)

1. A method of treating a hematologic malignancy in a mammal having said hematologic malignancy, comprising administering to the mammal a pharmaceutical composition comprising a therapeutically effective amount of a crystalline form of 1-(2R,4R)-2-(1H-benzo[d]imidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea maleate, having the structure:

and having a powder X-ray diffraction pattern comprising peaks at 2θ values of: 11.6, 12.1 and 19.6°2θ±0.2°2θ, and a pharmaceutically acceptable excipient.

2. A method of treating a hematologic malignancy in a mammal having said hematologic malignancy, comprising administering to the mammal a pharmaceutical composition comprising a therapeutically effective amount of a crystalline form of 1-(2R,4R)-2-(1H-benzo[d]imidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea maleate, having the structure:

and having: (a) a powder X-ray diffraction pattern comprising peaks at 2θ values of: 11.6 and 12.1°2θ±0.2°2θ; and (b) a Raman spectrum comprising wavenumber (cm −1 ) values of: 1612 and 2219 cm −1 ±2 cm −1 , and a pharmaceutically acceptable excipient.

3. A method of treating a hematologic malignancy in a mammal having said hematologic malignancy, comprising administering to the mammal a pharmaceutical composition comprising a therapeutically effective amount of a crystalline form of 1-(2R,4R)-2-(1H-benzo[d]imidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea maleate, having the structure:

and having: (a) a powder X-ray diffraction pattern comprising peaks at 28 values of: 11.6 and 12.1°2θ±0.2°2θ; (b) a Raman spectrum comprising wavenumber (cm −1 ) values of: 1612 and 2219 cm −1 ±2 cm −1 ; and (c) a 13 C solid state NMR spectrum comprising a resonance (ppm) value of: 148.3 ppm±0.2 ppm, and a pharmaceutically acceptable excipient.

4. A method of treating a hematologic malignancy in a mammal having said hematologic malignancy, comprising administering to the mammal a pharmaceutical composition comprising a therapeutically effective amount of a crystalline form of 1-((2R,4R)-2-(1H-benzo[d]imidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea maleate, having the structure:

and having: (a) a powder X-ray diffraction pattern comprising peaks at 28 values of: 11.6 and 12.1°2θ±0.2°2θ; and (b) a 13 C solid state NMR spectrum comprising a resonance (ppm) value of: 148.3 ppm±0.2 ppm, and a pharmaceutically acceptable excipient.

5. The method of claim 1 , wherein the pharmaceutical composition is suitable for oral administration.

6. The method of claim 2 , wherein the pharmaceutical composition is suitable for oral administration.

7. The method of claim 3 , wherein the pharmaceutical composition is suitable for oral administration.

8. The method of claim 4 , wherein the pharmaceutical composition is suitable for oral administration.

9. The method of claim 5 , wherein the pharmaceutical composition is a tablet.

10. The method of claim 6 , wherein the pharmaceutical composition is a tablet.

11. The method of claim 7 , wherein the pharmaceutical composition is a tablet.

12. The method of claim 8 , wherein the pharmaceutical composition is a tablet.

13. The method of claim 5 , wherein the mammal is a human.

14. The method of claim 6 , wherein the mammal is a human.

15. The method of claim 7 , wherein the mammal is a human.

16. The method of claim 8 , wherein the mammal is a human.

17. The method of claim 5 , wherein the hematologic malignancy is selected from the group consisting of acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelomonocytic leukemia, myelofibrosis and myelodysplastic syndrome.

18. The method of claim 6 , wherein the hematologic malignancy is selected from the group consisting of acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelomonocytic leukemia, myelofibrosis and myelodysplastic syndrome.

19. The method of claim 7 , wherein the hematologic malignancy is selected from the group consisting of acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelomonocytic leukemia, myelofibrosis and myelodysplastic syndrome.

20. The method of claim 8 , wherein the hematologic malignancy is selected from the group consisting of acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelomonocytic leukemia, myelofibrosis and myelodysplastic syndrome.

21. The method of claim 5 , wherein the hematologic malignancy is acute myeloid leukemia.

22. The method of claim 6 , wherein the hematologic malignancy is acute myeloid leukemia.

23. The method of claim 7 , wherein the hematologic malignancy is acute myeloid leukemia.

24. The method of claim 8 , wherein the hematologic malignancy is acute myeloid leukemia.

25. The method of claim 5 , wherein the hematologic malignancy is acute lymphoblastic leukemia.

26. The method of claim 6 , wherein the hematologic malignancy is acute lymphoblastic leukemia.

27. The method of claim 7 , wherein the hematologic malignancy is acute lymphoblastic leukemia.

28. The method of claim 8 , wherein the hematologic malignancy is acute lymphoblastic leukemia.

29. The method of claim 5 , wherein the hematologic malignancy is chronic myelomonocytic leukemia.

30. The method of claim 6 , wherein the hematologic malignancy is chronic myelomonocytic leukemia.

31. The method of claim 7 , wherein the hematologic malignancy is chronic myelomonocytic leukemia.

32. The method of claim 8 , wherein the hematologic malignancy is chronic myelomonocytic leukemia.

33. The method of claim 5 , wherein the hematologic malignancy is myelofibrosis.

34. The method of claim 6 , wherein the hematologic malignancy is myelofibrosis.

35. The method of claim 7 , wherein the hematologic malignancy is myelofibrosis.

36. The method of claim 8 , wherein the hematologic malignancy is myelofibrosis.

37. The method of claim 5 , wherein the hematologic malignancy is myelodysplastic syndrome.

38. The method of claim 6 , wherein the hematologic malignancy is myelodysplastic syndrome.

39. The method of claim 7 , wherein the hematologic malignancy is myelodysplastic syndrome.

40. The method of claim 8 , wherein the hematologic malignancy is myelodysplastic syndrome.

Assignments (2)
ASSIGNEE ADDRESS CORRECTION Recorded Mar 20, 2023
From: PFIZER INC.
To: PFIZER INC.
Reel/Frame 063119/0087 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2021
From: HANSEN, ERIC CHRISTIAN; SEADEEK, CHRISTOPHER SCOTT
To: PFIZER INC.
Reel/Frame 058308/0027 →