IP Library Granted Patent US 10,544,162
Granted Patent B2
US 10,544,162 · App. 15/998,872 · Granted Jan 28, 2020

Polymorphic form of TG02

Inventors: Robert K. Mansfield (San Marcos, CA); Tracy Parrott (San Diego, CA)
Assignee: ADASTRA PHARMACEUTICALS, INC.
C07D498/08A61K31/529A61K45/06C07B2200/13
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Quick Facts
Patent No.
US 10,544,162
App. No.
15/998,872
Granted
Jan 28, 2020
Kind
B2
Abstract

The present disclosure provides crystalline polymorphic forms of TG02 free base and TG02 acid addition salts, pharmaceutical compositions comprising crystalline polymorphic forms of TG02 free base and TG02 acid addition salts, and methods of treating cancer and other diseases in a patient with crystalline polymorphic forms of TG02 free base and TG02 acid addition salts.

Claims (29)

1. A crystalline polymorphic form of the citrate salt of (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene characterized as having a powder x-ray diffraction pattern with peaks at 15.2, 15.5, 21.7, 22.1, 23.0, 26.2, and 29.9 degrees 2Θ.

2. The crystalline polymorphic form of claim 1 having an average particle size distribution of about 10 μm or less.

3. The crystalline polymorphic form of claim 2 having an average particle size distribution of about 1 μm or less.

4. A pharmaceutical composition comprising the crystalline polymorphic form of claim 1 and one or more pharmaceutically acceptable excipients.

5. The pharmaceutical composition of claim 4 comprising, by weight:

(a) about 7% to about 70% of the crystalline polymorphic form;

(b) about 20% to about 83% of a filler;

(c) about 1% to about 10% of a disintegrant;

(d) about 1% to about 10% of a binder; and

(e) about 0.1% to about 1% of a lubricant.

6. A kit comprising the crystalline polymorphic form of claim 1 and instructions for administering the crystalline polymorphic form to a patient having cancer.

7. The kit of claim 6 further comprising an immune checkpoint inhibitor or alkylating agent.

8. A method of making the pharmaceutical composition of claim 4 , the method comprising admixing the crystalline polymorphic form and one or more pharmaceutically acceptable excipients.

9. A method of making the crystalline polymorphic form of claim 1 , the method comprising:

(a) combining a solution of citric acid in ethanol with a solution of (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene free base in DMSO/ethanol;

(b) heating the solution of (a) at about 70° C. for at least about 15 minutes to give a solution comprising (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene citrate;

(c) cooling the solution of (b) comprising (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene citrate to about 5° C. to give a crystalline solid; and

(d) isolating the crystalline solid of (c) to give the crystalline polymorphic form.

10. The pharmaceutical composition of claim 5 comprising, by weight, about 60% to about 65% of the crystalline polymorphic form.

11. The pharmaceutical composition of claim 10 comprising, by weight, about 25% to about 30% of a filler.

12. The pharmaceutical composition of claim 11 , wherein the filler is selected from the group consisting of microcrystalline cellulose, silicified microcrystalline cellulose, lactose monohydrate, and mannitol.

13. The pharmaceutical composition of claim 12 comprising, by weight: (a) about 63.5% of the crystalline polymorphic form; (b) about 26% of silicified microcrystalline cellulose; (c) about 5% of crospovidone; (d) about 5% of hydroxypropyl methylcellulose; and (e) about 0.5% of magnesium stearate.

14. The pharmaceutical composition of claim 5 comprising, by weight, about 35% to about 40% of the crystalline polymorphic form.

15. The pharmaceutical composition of claim 14 comprising, by weight, about 50% to about 55% of a filler.

16. The pharmaceutical composition of claim 15 , wherein the filler is selected from the group consisting of microcrystalline cellulose, silicified microcrystalline cellulose, lactose monohydrate, and mannitol.

17. The pharmaceutical composition of claim 16 comprising, by weight: (a) about 36.3% of the crystalline polymorphic form; (b) about 53.2% of silicified microcrystalline cellulose; (c) about 5% of crospovidone; (d) about 5% of hydroxypropyl methylcellulose; and (e) about 0.5% of magnesium stearate.

18. The pharmaceutical composition of claim 5 comprising, by weight, about 7% to about 10% of the crystalline polymorphic form.

19. The pharmaceutical composition of claim 18 comprising, by weight: (a) about 7.5% of the crystalline polymorphic form; (b) about 82% of silicified microcrystalline cellulose; (c) about 5% of crospovidone; (d) about 5% of hydroxypropyl methylcellulose; and (e) about 0.5% of magnesium stearate.

20. The pharmaceutical composition of claim 5 for oral administration in a capsule.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2021
From: ADASTRA PHARMACEUTICALS, INC.
To: COTHERA BIOSCIENCE, INC.
Reel/Frame 057502/0723 →
CHANGE OF NAME Recorded Oct 8, 2019
From: TRAGARA PHARMACEUTICALS, INC.
To: ADASTRA PHARMACEUTICALS, INC.
Reel/Frame 050660/0143 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2019
From: MANSFIELD, ROBERT K.; PARROTT, TRACY
To: TRAGARA PHARMACEUTICALS, INC.
Reel/Frame 048322/0493 →
Continuity (2)
Provisional Application 62547157 · Aug 18, 2017
Related Publication 20190055263A1 · Feb 21, 2019