IP Library Granted Patent US 10,676,506
Granted Patent B2
US 10,676,506 · App. 16/259,575 · Granted Jun 9, 2020

Crystalline bis- and tris-hydrochloride salt of elamipretide

Inventor: Scott M. Duncan (Bedford, MA)
Assignee: Stealth BioTherapeutics Corp.
C07K5/1019C07K1/14C07B2200/13
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Quick Facts
Patent No.
US 10,676,506
App. No.
16/259,575
Granted
Jun 9, 2020
Kind
B2
Abstract

Disclosed are crystalline forms of the bis- and tris-(hydrochloride) salts of D-Arg-Tyr(2,6-DiMe)-Lys-Phe-NH 2 , which is also known as MTP-131.

Claims (297)

1. A crystalline form of a bis-(hydrochloride) salt of Compound (I),

wherein said crystalline form has peaks in its XRPD pattern at values of two theta as listed in Table 2A:

TABLE 2A

d spacing

Height

Relative intensity

2θ (°)

(A°)

(cps)

(%)

6.40

13.79726

1343

28

6.98

12.65711

406

9

7.88

11.20719

160

3

9.05

9.76484

112

2

9.84

8.97904

1550

33

10.18

8.67918

186

4

11.65

7.58843

340

7

13.06

6.77213

4732

100

16.88

5.24746

715

15

19.09

4.64608

790

17

20.61

4.30611

289

6

24.21

3.67305

113

2

24.84

3.58126

433

9

26.33

3.38163

298

6

27.44

3.24777

327

7

28.59

3.11934

158

3

29.73

3.00251

480

10.

2. A crystalline form of a bis-(hydrochloride) salt of Compound (I),

wherein said crystalline form has peaks in its XRPD pattern as shown in FIG. 2 .

3. A crystalline form of a bis-(hydrochloride) salt of Compound (I),

wherein said crystalline form has peaks in its XRPD pattern at values of two theta (° 2) of: 6.4, 9.8, 13.1, 16.9, 19.1, and 29.7.

4. The crystalline form of claim 3 , wherein said crystalline form has peaks in its XRPD pattern at values of two theta (° 2) of: 6.4, 7.0, 7.9, 9.1, 9.8, 10.2, 11.7, 13.1, 16.9, 19.1, 20.6, 24.2, 24.8, 26.3, 27.4, 28.6, and 29.7.

5. A crystalline form of a tris-(hydrochloride) salt of Compound (I),

wherein said crystalline form has peaks in its XRPD pattern at values of two theta as listed in Table 10A:

TABLE 10A

Pos.

d-spacing

Height

Rel. Int.

[°2θ]

[Å]

[cts]

[%]

5.6826

15.55252

48.89

5.06

6.669

13.25428

16.7

1.73

8.1507

10.84783

650.66

67.29

9.2697

9.54072

154.41

15.97

9.8231

9.00438

277.37

28.68

11.0495

8.00758

264.45

27.35

11.4729

7.713

393.18

40.66

12.3925

7.14266

360.31

37.26

12.8405

6.89444

63.27

6.54

13.6472

6.48865

237.2

24.53

14.3699

6.16392

107.3

11.1

14.8755

5.95554

245.56

25.39

15.5909

5.68384

369.87

38.25

15.8566

5.58918

690.32

71.39

17.1543

5.16919

226.03

23.38

17.5374

5.05713

195.25

20.19

17.953

4.94097

47.6

4.92

18.525

4.78968

58.51

6.05

18.9247

4.68942

87.39

9.04

19.3114

4.59638

76.49

7.91

19.6517

4.51754

125.18

12.95

20.1474

4.40749

317.33

32.82

20.3935

4.35487

89.76

9.28

20.6086

4.3099

83.34

8.62

21.1328

4.20415

68.92

7.13

21.8535

4.06712

319.84

33.08

22.1439

4.01443

737.79

76.3

22.6006

3.93432

204.99

21.2

23.0153

3.86436

966.96

100

23.4697

3.79057

560.81

58

23.9736

3.71203

182.25

18.85

24.2292

3.67344

181.59

18.78

24.8488

3.58324

192.35

19.89

25.46

3.49858

152.72

15.79

25.8659

3.44459

116.17

12.01

26.4139

3.37436

205.95

21.3

26.945

3.30905

134.94

13.96

27.4489

3.24943

407.87

42.18

27.9725

3.18979

284.45

29.42

28.1692

3.16796

237.71

24.58

28.7691

3.10326

99.86

10.33

29.6808

3.00998

36.29

3.75

30.7678

2.90607

48.38

5

31.7169

2.82124

134.12

13.87

33.0072

2.71384

72.56

7.5

33.8578

2.64759

76.16

7.88.

6. A crystalline form of a tris-(hydrochloride) salt of Compound (I),

wherein said crystalline form has peaks in its XRPD pattern as shown in FIG. 9 .

7. A crystalline form of a tris-(hydrochloride) salt of Compound (I),

wherein said crystalline form has peaks in its XRPD pattern at values of two theta (° 2) of: 8.1, 11.5, 15.6, 15.9, 22.1, 23.0, and 27.4.

8. The crystalline form of claim 7 , wherein said crystalline form has peaks in its XRPD pattern at values of two theta (° 2) of: 8.1, 9.8, 11.0, 11.5, 12.4, 14.9, 15.6, 15.9, 20.1, 21.8, 22.1, 23.0, 27.4, and 28.0.

9. A composition, comprising the crystalline form of claim 1 .

10. A process for making a pharmaceutical composition comprising Compound (I),

which comprises dissolving the crystalline form of claim 1 .

11. A process for making a pharmaceutical composition comprising Compound (I),

which comprises dissolving the crystalline form of claim 5 .

12. A process for making a pharmaceutical composition comprising Compound (I),

which comprises dissolving the crystalline form of claim 1 .

13. A composition, comprising the crystalline form of claim 2 .

14. A composition, comprising the crystalline form of claim 3 .

15. A composition, comprising the crystalline form of claim 4 .

16. A composition, comprising the crystalline form of claim 5 .

17. A composition, comprising the crystalline form of claim 6 .

18. A composition, comprising the crystalline form of claim 7 .

19. A composition, comprising the crystalline form of claim 8 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2021
From: STEALTH BIOTHERAPEUTICS CORP.
To: STEALTH BIOTHERAPEUTICS INC.
Reel/Frame 058601/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2019
From: DUNCAN, SCOTT M.
To: STEALTH BIOTHERAPEUTICS CORP.
Reel/Frame 049547/0537 →
Continuity (3)
Provisional Application 62656649 · Apr 12, 2018
Provisional Application 62622259 · Jan 26, 2018
Related Publication 20190233474A1 · Aug 1, 2019
Cited By (1)
US 12,252,553