IP Library Patent Application 18276709
Patent Application
App. No. 18/276,709

PHARMACEUTICALLY ACCEPTABLE SALTS OF PSILOCIN AND USES THEREOF

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Patent No.
US None
App. No.
18/276,709
Abstract

The present invention composition features pharmaceutically acceptable salts of psilocin and compositions thereof. The pharmaceutically acceptable salts of psilocin may be used to treat a disease or condition, such as a neurological injury, an inflammatory condition, chronic pain, or a psychological condition, in a subject in need thereof.

Claims (33)

1 . A pharmaceutically acceptable salt of psilocin, wherein said pharmaceutically acceptable salt is a 1:1 benzoate salt.

2 . A pharmaceutically acceptable salt of psilocin, wherein said pharmaceutically acceptable salt is a 1:1 tartrate salt.

3 . A pharmaceutically acceptable salt of psilocin, wherein said pharmaceutically acceptable salt is a 2:1 succinate salt.

4 . A pharmaceutically acceptable salt of psilocin, wherein said pharmaceutically acceptable salt is a 2:1 salt of 1,5-naphthalenedisulfonic acid, a 1:1 salt of 1,5-naphthalenedisulfonic acid, or a mixture thereof.

5 . A pharmaceutical composition comprising a psilocin salt of any one of claims 1 - 4 and a pharmaceutically acceptable excipient.

6 . A pharmaceutical composition comprising (i) an aqueous solution having a pH of between about 3 and about 9 and (ii) between about 0.1 mg/mL and about 50 mg/mL of a psilocin salt of any one of claims 1 - 4 , wherein the pharmaceutical composition is suitable for infusion.

7 . The pharmaceutical composition of claim 6 , wherein the aqueous solution has between about 1 mg/mL and about 15 mg/mL.

8 . A crystal form of a 2:1 succinate salt of psilocin having at least four, five, six, or seven peaks at diffraction angle 2θ (°) as provided in FIG. 4 (SUC Pattern 4) as measured by X-ray powder diffractometry.

9 . A crystal form of a 1,5-naphthalenedisulfonic acid salt of psilocin having at least four, five, six, or seven peaks at diffraction angle 2θ (°) as provided in FIG. 7 or FIG. 14 (NAP Pattern 1) as measured by X-ray powder diffractometry.

10 . A crystal form of a 1:1 tartrate salt of psilocin having at least four, five, six, or seven peaks at diffraction angle 2θ (°) as provided in FIG. 9 or FIG. 12 (TAR Pattern 3) as measured by X-ray powder diffractometry.

11 . A crystal form of a 1:1 tartrate salt of psilocin having at least four, five, six, or seven peaks at diffraction angle 2θ (°) as provided in FIG. 10 (TAR Pattern 4) as measured by X-ray powder diffractometry.

12 . A crystal form of a 1:1 tartrate salt of psilocin having at least four, five, six, or seven peaks at diffraction angle 2θ (°) selected from 6.7±0.5, 12.6±0.5, 13.4±0.5, 14.7±0.5, 15.8±0.5, 16.2±0.5, 17.2±0.5, 18.8±0.5, 19.9±0.5, 20.8±0.5, 21.8±0.5, 22.5±0.5, 23.4±0.5, 23.7±0.5, 24.7±0.5, 25.5±0.5, 26.5±0.5, 27.0±0.5, 28.5±0.5, and 29.4±0.5 (TAR Pattern 1) as measured by X-ray powder diffractometry.

13 . A crystal form of a 2:1 succinate salt of psilocin having at least four, five, six, or seven peaks at diffraction angle 2θ (°) selected from 9.7±0.5, 11.2±0.5, 12.3±0.5, 13.8±0.5, 15.9±0.5, 16.4±0.5, 19.4±0.5, 20.0±0.5, 21.3±0.5, 22.6±0.5, 23.3±0.5, 23.5±0.5, 23.8±0.5, 24.5±0.5, 24.7±0.5, 25.0±0.5, 28.0±0.5, 28.3±0.5, 29.00±0.5, and 29.4±0.5 (SUC Pattern 3) as measured by X-ray powder diffractometry.

14 . A crystal form of a 1:1 benzoate salt of psilocin having at least four, five, six, or seven peaks at diffraction angle 2θ (°) 9.4±0.5, 10.9±0.5, 12.3±0.5, 13.3±0.5, 14.5±0.5, 15.3±0.5, 16.3±0.5, 16.4±0.5, 18.2±0.5, 18.9±0.5, 19.3±0.5, 19.7±0.5, 20.0±0.5, 20.8±0.5, 21.3±0.5, 21.9±0.5, 22.6±0.5, 22.9±0.5, 23.8±0.5, 24.1±0.5, 24.9±0.5, 25.6±0.5, 26.0±0.5, 26.3±0.5, 26.5±0.5, 26.9±0.5, 27.5±0.5, and 28.5±0.5 (BEN Pattern 1) as measured by X-ray powder diffractometry.

15 . A pharmaceutical composition comprising a crystal form of any one of claims 8 - 14 and a pharmaceutically acceptable excipient.

16 . The pharmaceutical composition of any of one of claims 1 - 6 or 15 , wherein the pharmaceutical composition is stored in an amber bottle.

17 . A method of treating a disease or condition a subject in need thereof, the method comprising administering to the subject a pharmaceutical composition of any one of claim 5 - 7 or 15 in an amount sufficient to treat the disease or condition.

18 . The method of claim 17 , wherein the disease or condition is a neurological injury, a neurodegenerative disease, an inflammatory condition, chronic pain, or a psychological condition.

19 . The method of claim 17 , wherein the disease or condition is an inflammatory condition.

20 . The method of claim 19 , wherein the inflammatory condition is lung inflammation, neuroinflammation, rheumatoid arthritis, atherosclerosis, psoriasis, type II diabetes, inflammatory bowel disease, Crohn's disease, multiple sclerosis, and/or septicemia.

21 . The method of claim 19 , wherein the inflammatory condition is chronic obstructive pulmonary disease (COPD), or Alzheimer's disease.

22 . The method of claim 17 , wherein the disease or condition is a neurological injury.

23 . The method of claim 22 , wherein the neurological injury is a stroke, a traumatic brain injury, or a spinal cord injury.

24 . The method of claim 17 , wherein the disease or condition is chronic pain.

25 . The method of claim 24 , wherein the chronic pain results from post-operative pain, tension headaches, chronic lower back pain, fibromyalgia, nephropathy, multiple sclerosis, shingles, complex regional pain syndrome, cephalic pain, or sciatica.

26 . The method of claim 25 , wherein the chronic pain condition results from trigeminal autonomic cephalalgia.

27 . The method of claim 26 , wherein the trigeminal autonomic cephalalgia is selected from the group consisting of episodic and chronic cluster headache (CH), episodic and chronic paroxysmal hemicrania (PH), and short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT).

28 . The method of claim 27 , wherein the trigeminal autonomic cephalalgia is episodic or chronic CH.

29 . The method of claim 17 wherein the condition is a psychological condition.

30 . The method of claim 29 , wherein the psychological condition is depression, anxiety, addiction, post-traumatic stress disorder, an eating disorder, or compulsive behavior.

31 . The method of claim 30 , wherein the psychological condition is depression.

32 . The method of claim 29 , wherein the psychological condition is anxiety.

33 . The method of claim 17 , wherein the disease or condition is a neurodegenerative disease selected from Alzheimer's disease, Huntington's disease, and Parkinson's disease.