IP Library › Granted Patent US 12,168,666
Granted Patent B2
US 12,168,666 · App. 17/236,687 · Granted Dec 17, 2024

Morphic forms of trilaciclib and methods of manufacture thereof

Inventors: Stephen Schneider (Raleigh, NC); Alexander Smith (Apex, NC); Hannah S. White (Chapel Hill, NC); Jay Copeland Strum (Hillsborough, NC); Jaroslaw Mazurek (Amsterdam, NL)
Assignee: G1 Therapeutics, Inc.
C07D487/20A61K9/0019A61K9/08A61K9/19A61K47/02A61K47/12A61K47/26C07B2200/13
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Quick Facts
Patent No.
US 12,168,666
App. No.
17/236,687
Granted
Dec 17, 2024
Kind
B2
Abstract

An advantageous isolated morphic form of trilaciclib which is 2′-((5-(4-methylpiperazin-1-yl)pyridin-2-yl)amino)-7′,8′-dihydro-6′H-spiro[cyclohexane-1,9′-pyrazino[1′,2′:1,5]pyrrolo[2,3-d]pyrimidin]-6′-one, for example in the form of a di-hydrochloride salt or a dihydrochloride, dihydrate.

Claims (28)

1. A crystalline compound of structure:

which is a dihydrochloride.

2. The crystalline compound of claim 1 characterized by an X-ray powder diffraction (XRPD) pattern comprising at least three 2theta values selected from 9.6±0.2°, 21.3±0.2°, 19.8±0.2°, 12.2±0.2°, 24.0±0.2°, 26.1±0.2°, 19.3±0.2°, 17.6±0.2°, and 28.6±0.2°.

3. The crystalline compound of claim 2 , wherein the XRPD pattern comprises at least four 2theta values selected from 9.6±0.2°, 21.3±0.2°, 19.8±0.2°, 12.2±0.2°, 24.0±0.2°, 26.1±0.2°, 19.3±0.2°, 17.6±0.2°, and 28.6±0.2°.

4. The crystalline compound of claim 2 , wherein the XRPD pattern comprises at least five 2theta values selected from 9.6±0.2°, 21.3±0.2°, 19.8±0.2°, 12.2±0.2°, 24.0±0.2°, 26.1±0.2°, 19.3±0.2°, 17.6±0.2°, and 28.6±0.2°.

5. The crystalline compound of claim 2 , wherein the XRPD pattern comprises at least six 2theta values selected from 9.6±0.2°, 21.3±0.2°, 19.8±0.2°, 12.2±0.2°, 24.0±0.2°, 26.1±0.2°, 19.3±0.2°, 17.6±0.2°, and 28.6±0.2°.

6. The crystalline compound of claim 2 , wherein the XRPD pattern comprises at least the 2theta value of 9.6±0.2°.

7. The crystalline compound of claim 2 , wherein the XRPD pattern comprises at least the 2theta values of 9.6±0.2°, 19.8±0.2°, and 21.3±0.2°.

8. A composition comprising the crystalline compound of claim 1 , mannitol and citric acid.

9. A pharmaceutical composition comprising the crystalline compound of claim 1 and a pharmaceutically acceptable excipient.

10. The pharmaceutical composition of claim 9 , wherein the pharmaceutically acceptable excipient comprises mannitol.

11. The pharmaceutical composition of claim 9 , wherein the pharmaceutically acceptable excipient comprises citric acid.

12. The pharmaceutical composition of claim 9 , wherein the pharmaceutically acceptable excipient comprises mannitol and citric acid.

13. The pharmaceutical composition of claim 9 comprising about 200-600 milligrams of the crystalline compound.

14. The pharmaceutical composition of claim 9 comprising about 300 milligrams of the crystalline compound.

15. The pharmaceutical composition of claim 9 comprising about 349 milligrams of the crystalline compound.

16. The pharmaceutical composition of claim 10 comprising about 250-350 mg of mannitol.

17. The pharmaceutical composition of claim 10 comprising about 300 mg of mannitol.

18. The pharmaceutical composition of claim 11 comprising about 50-100 mg of citric acid.

19. The pharmaceutical composition of claim 11 comprising about 76 mg of citric acid.

20. The pharmaceutical composition of claim 12 comprising about 250-350 mg of mannitol.

21. The pharmaceutical composition of claim 12 comprising about 300 mg of mannitol.

22. The pharmaceutical composition of claim 12 comprising about 50-100 mg of citric acid.

23. The pharmaceutical composition of claim 12 comprising about 76 mg of citric acid.

24. The pharmaceutical composition of claim 12 comprising about 300 mg of mannitol and about 76 mg of citric acid.

25. The pharmaceutical composition of claim 24 comprising about 300 milligrams of the crystalline compound.

26. The pharmaceutical composition of claim 12 comprising a dose of about 150 mg/m 2 to about 350 mg/m 2 of the crystalline compound.

27. The pharmaceutical composition of claim 12 comprising a dose of about 240 mg/m 2 of the crystalline compound.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 23, 2025
From: PHARMACOSMOS THERAPEUTICS, INC.
To: PHARMACOSMOS A/S
Reel/Frame 071018/0421 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 23, 2025
From: PHARMACOSMOS A/S
To: PHARMACOSMOS HOLDING A/S
Reel/Frame 071018/0502 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2024
From: G1 THERAPEUTICS, INC.
To: PHARMACOSMOS A/S
Reel/Frame 069502/0317 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2024
From: PHARMACOSMOS A/S
To: PHARMACOSMOS HOLDING A/S
Reel/Frame 069502/0326 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2024
From: ARDENA HOLDING NV
To: G1 THERAPEUTICS, INC.
Reel/Frame 067325/0873 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2024
From: MAZUREK, JAROSLAW
To: ARDENA HOLDING NV
Reel/Frame 067329/0367 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2024
From: SCHNEIDER, STEPHEN; SMITH, ALEXANDER; WHITE, HANNAH S.; STRUM, JAY COPELAND
To: G1 THERAPEUTICS, INC.
Reel/Frame 067325/0814 →
Continuity (3)
Continuation 17097854 · Nov 13, 2020
Provisional Application 63039372 · Jun 15, 2020
Related Publication 20210387993A1 · Dec 16, 2021
Cited By (4)
US 12,479,855 US 12,497,404 US 12,527,798 US 12,534,472