IP Library Granted Patent US 9,376,419
Granted Patent B2
US 9,376,419 · App. 14/436,049 · Granted Jun 28, 2016

Solid forms of nilotinib hydrochloride

Inventors: Probal Kanti Datta (Hamilton, CA); Carlos Zetina-Rocha (Burnaby, CA); Cameron L. McPhail (Brantford, CA); Yajun Zhao (Brantford, CA); Gamini Weeratunga (Ancaster, CA)
Assignee: Apotex Inc.
C07D401/14C07B2200/13
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 9,376,419
App. No.
14/436,049
Granted
Jun 28, 2016
Kind
B2
Abstract

Disclosed are solid forms of Nilotinib hydrochloride and methods of preparation of various crystalline solvates of Nilotinib HCl including benzyl alcohol, acetic acid, propylene glycol, and isopropanol. Nilotinib HCl is a tyrosine kinase inhibitor used for the treatment of drug resistant chronic myelogenous leukemia (CML).

Claims (18)

1. A crystalline solid form of Nilotinib hydrochloride having an X-ray powder diffraction pattern comprising peaks, in terms of degrees 2 -theta, at approximately 6.0, 6.5, 18.1, 19.5, 20.8 and 25.3.

2. The crystalline solid form of Nilotinib hydrochloride of claim 1 having an X-ray powder diffraction pattern as shown in FIG. 1 .

3. The crystalline solid form of Nilotinib hydrochloride of claim 1 wherein the crystalline solid form of Nilotinib hydrochloride is a benzyl alcohol solvate wherein the molar ratio of Nilotinib hydrochloride to benzyl alcohol is approximately 1:1.

4. A crystalline solid form of Nilotinib hydrochloride having an X-ray powder diffraction pattern comprising peaks, in terms of degrees 2 -theta, at approximately 7.5, 9.1, 11.0, 19.6, 20.8, 21.8, and 24.1.

5. The crystalline solid form of Nilotinib hydrochloride of claim 4 having an X-ray powder diffraction pattern as shown in FIG. 2 .

6. The crystalline solid form of Nilotinib hydrochloride of claim 4 having a differential scanning calorimetry thermogram comprising an endothermic peak with an onset temperature of approximately 134° C.

7. The crystalline solid form of Nilotinib hydrochloride of claim 4 having a differential scanning calorimetry thermogram as shown in FIG. 3 .

8. The crystalline solid form of Nilotinib hydrochloride of claim 4 wherein the crystalline solid form of Nilotinib hydrochloride is a propylene glycol solvate wherein the molar ratio of propylene glycol to Nilotinib hydrochloride is approximately 1:1.

9. A crystalline solid form of Nilotinib hydrochloride having an X-ray powder diffraction pattern comprising peaks, in terms of degrees 2 -theta, at approximately 6.2, 12.5, 18.8, 22.0, 24.0, and 26.0.

10. The crystalline solid form of Nilotinib hydrochloride of claim 9 having an X-ray powder diffraction pattern as shown in FIG. 4 .

11. The crystalline solid form of Nilotinib hydrochloride of claim 9 wherein crystalline solid form of Nilotinib hydrochloride comprises acetic acid salt wherein the molar ratio of acetic acid to Nilotinib hydrochloride is approximately 2:1.

12. A crystalline solid form of Nilotinib hydrochloride having an X-ray powder diffraction pattern comprising peaks, in terms of degrees 2 -theta, at approximately 6.8, 9.2, 13.1, 13.9, 17.9 and 25.3.

13. The crystalline solid form of Nilotinib hydrochloride of claim 12 having an X-ray powder diffraction pattern as shown in FIG. 5 .

14. The crystalline solid form of Nilotinib hydrochloride of claim 12 having a differential scanning calorimetry thermogram comprising an endothermic peak with an onset temperature of approximately 210° C.

15. The crystalline solid form of Nilotinib hydrochloride of claim 12 having a differential scanning calorimetry thermogram as shown in FIG. 6 .

16. A crystalline solid form of Nilotinib hydrochloride having an X-ray powder diffraction pattern comprising peaks, in terms of degrees 2 -theta, at approximately 7.2, 9.6, 16.0, 17.6, 21.8, and 26.0.

17. The crystalline solid form of Nilotinib hydrochloride of claim 16 having an X-ray powder diffraction pattern as shown in FIG. 7 .

18. The crystalline solid form of Nilotinib hydrochloride of claim 16 wherein the crystalline solid form of Nilotinib hydrochloride comprises acetic acid salt wherein the molar ratio of acetic acid to Nilotinib hydrochloride is approximately 1:1.

Assignments (3)
SECURITY INTEREST Recorded Apr 15, 2023
From: APOTEX INC.
To: THE BANK OF NOVA SCOTIA
Reel/Frame 063364/0710 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2015
From: DATTA, PROBAL KANTI; ZETINA-ROCHA, CARLOS; MCPHAIL, CAMERON L.; ZHAO, YAJUN; WEERATUNGA, GAMINI
To: APOTEX TECHNOLOGIES INC.
Reel/Frame 036439/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2015
From: APOTEX TECHNOLOGIES INC.
To: APOTEX INC.
Reel/Frame 036439/0604 →
Continuity (2)
Provisional Application 61714120 · Oct 15, 2012
Related Publication 20150274699A1 · Oct 1, 2015