IP Library Granted Patent US 12,370,166
Granted Patent B2
US 12,370,166 · App. 17/816,950 · Granted Jul 29, 2025

Pentadecanoylcarnitine for treatment of conditions related to the quality of aging and longevity

Inventor: Stephanie Venn-Watson (San Diego, CA)
Assignee: Epitracker, Inc.
A61K31/23A61K31/20A61P9/00A61P11/06A61P13/12A61P17/06A61P25/16A61P25/24A61P37/06A61P37/08
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Quick Facts
Patent No.
US 12,370,166
App. No.
17/816,950
Granted
Jul 29, 2025
Kind
B2
Abstract

Administration of pentadecanoylcarnitine or pentadecanoic acid is provided for prevention, management or treatment of aggression, allergies, allergic rhinitis, Alzheimer's disease, anxiety and anxiety disorders, amyotrophic lateral sclerosis, arthritis, asthma, atherosclerosis, attention-deficit hyperactivity disorder, bipolar disorder, brain damage, cancer, cardiovascular disease, cholestatic pruritis, depression, chronic obstructive pulmonary disease (COPD), cocaine abuse, cough, dermatitis, depression, drug-seeking behavior, gastrointestinal disorders, facial erythema associated with rosacea, glaucoma, hepatic diseases, hyperactive bladder, hypersensitivity disorders, hypertension, impulsivity, inflammation, mental disorders and conditions, metabolic disorders, migraines, nasal and sinus congestion, nausea, neuropathic pain with and symptoms of multiple sclerosis, neurological and neuropsychiatric disorders, obesity, obsessive-compulsive disorders, opioid-induced respiratory depression, osteoarthritis, pain, Parkinson disease, pathological gambling, peptic ulcers, schizophrenia, sleep disorders, spinal cord injury, tardive dyskinesia, tics and behavioral problems with Tourette's syndrome; as well as for supporting appetite, cardiovascular health, hematologic health, memory, metabolic health, mood, prolonged REM sleep, renal health, sexuality, sociability and metabolic, hematological, renal, and weight loss.

Claims (32)

1. A method of treatment, management, or amelioration of a condition selected from the group consisting of aggression, anxiety, anxiety disorders, attention-deficit hyperactivity disorder, bipolar disorder, brain damage, cholestatic pruritis, depression, cocaine abuse, drug-seeking behavior, facial erythema associated with rosacea, glaucoma, hyperactive bladder, hypertension, impulsivity, mental disorders, mental conditions, migraines, nasal congestion, sinus congestion, obsessive-compulsive disorders, opioid-induced respiratory depression, osteoarthritis, pathological gambling, schizophrenia, spinal cord injury, tardive dyskinesia, tics with Tourette's syndrome, and behavioral problems with Tourette's syndrome, the method comprising:

administering to a subject in need thereof, an effective amount of pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof.

2. The method of claim 1 , wherein a body concentration of pentadecanoylcarnitine of from 1 μM to 20 μM is achieved in the subject.

3. The method of claim 1 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered.

4. The method of claim 1 , wherein from 0.1 mg to 50 mg, per 1 kg of body weight, of the pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof is administered.

5. The method of claim 1 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof is administered once per day.

6. The method of claim 1 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof is in a unit dosage form comprising from 0.01 mg to 10000 mg, of the pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof.

7. The method of claim 1 , wherein the condition is selected from the group consisting of aggression, anxiety, anxiety disorders, attention-deficit hyperactivity disorder, cholestatic pruritis, depression, cocaine abuse, drug-seeking behavior, glaucoma, hyperactive bladder, hypertension, impulsivity, mental disorders, mental conditions, migraines, obsessive-compulsive disorders, opioid-induced respiratory depression, pathological gambling, schizophrenia, tardive dyskinesia, tics with Tourette's syndrome, and behavioral problems with Tourette's syndrome.

8. The method of claim 1 , wherein the condition is selected from anxiety disorders, attention-deficit hyperactivity disorder, depression, brain damage, glaucoma, tardive dyskinesia, cholestatic pruritis, tics with Tourette's syndrome, and behavioral problems with Tourette's syndrome.

9. The method of claim 1 , wherein the condition is selected from aggression, anxiety, bipolar disorder, depression, drug-seeking behavior, hypertension, migraines, opioid-induced respiratory depression, and schizophrenia.

10. The method of claim 1 , wherein the condition is selected from anxiety, depression, aggression, and impulsivity.

11. The method of claim 1 , wherein the condition is selected from facial erythema associated with rosacea, nasal congestion, and sinus congestion.

12. The method of claim 1 , wherein the condition is selected from cocaine abuse, pathological gambling, obsessive-compulsive disorder, and schizophrenia.

13. The method of claim 1 , wherein the condition is obsessive-compulsive disorder.

14. The method of claim 1 , wherein the condition is hyperactive bladder or depression.

15. The method of claim 1 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered as a dietary supplement.

16. The method of claim 1 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered in a unit dosage form.

17. The method of claim 1 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered in a tablet, a capsule, an encapsulated pill, a gelcap pill, a dispensable form of an oral or injectable liquid suspension or solution, a spray, an aerosol, powder, or granules.

18. The method of claim 1 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is isolated from natural sources, semi-synthetic, synthetic, or any mixture thereof.

19. A method of supporting appetite, memory, mood, renal health, sexuality, sociability, or weight loss, the method comprising:

administering to a subject in need thereof, an effective amount of pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof.

20. The method of claim 19 , wherein a body concentration of pentadecanoylcarnitine of from 1 μM to 20 μM is achieved in the subject.

21. The method of claim 19 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered.

22. The method of claim 19 , wherein from 0.1 mg to 50 mg, per 1 kg of body weight, of the pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof is administered.

23. The method of claim 19 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt or solvate thereof is administered once per day.

24. The method of claim 19 , wherein pentadecanoylcarnitine or or pharmaceutically acceptable salts, solvates, or stereoisomers thereof is in a unit dosage form comprising from 0.01 mg to 10000 mg, of the pentadecanoylcarnitine or pharmaceutically acceptable salts, solvates, stereoisomers, or esters thereof.

25. The method of claim 19 , wherein the method supports appetite, mood, renal health, sexuality, or sociability.

26. The method of claim 19 , wherein the method supports appetite, sexuality, or sociability.

27. The method of claim 19 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered as a dietary supplement.

28. The method of claim 19 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered in a unit dosage form.

29. The method of claim 19 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is administered in a tablet, a capsule, an encapsulated pill, a gelcap pill, a dispensable form of an oral or injectable liquid suspension or solution, a spray, an aerosol, powder, or granules.

30. The method of claim 19 , wherein pentadecanoylcarnitine or a pharmaceutically acceptable salt thereof is isolated from natural sources, semi-synthetic, synthetic, or any mixture thereof.

Continuity (3)
Provisional Application 63340710 · May 11, 2022
Provisional Application 63275353 · Nov 3, 2021
Related Publication 20230132955A1 · May 4, 2023
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