Granted Patent B2

US 12,263,155 · App. 18/616,046 · Granted Apr 1, 2025

Inventors: Tom Spector (Chapel Hill, NC); Jeremy Ford (Norwell, MA); Thomas A. Krenitsky (Chapel Hill, NC)

Assignee: Remedi, Inc.

A61K31/39A61K31/4045A61P25/24

Abstract

Claims (23)

1. A pharmaceutical composition or kit of parts, useful to treat a mental health disorder in a human, comprising therapeutically effective amounts of:

a) a compound having the formula:

(CX157), or a pharmaceutically acceptable salt thereof; and

b) N,N-dimethyltryptamine (DMT), or a pharmaceutically acceptable salt thereof;

wherein the DMT is formulated for oral administration.

2. A method of treating a mental health in a subject, comprising administering to the subject the composition or kit of parts of claim 1 .

3. The method of claim 2 , wherein the CX157 is administered prior to administration of the DMT.

4. The method of claim 2 , wherein the mental health disorder is any of post-traumatic stress disorder (PTSD), an adjustment disorder, an affective disorder, a depressive disorder, major depressive disorder (MDD), treatment-resistant depression (TRD), atypical depression, postpartum depression, catatonic depression, a depressive disorder due to a medical condition, premenstrual dysphoric disorder, seasonal affective disorder, dysthymia, an anxiety disorder, an anxiety related disorder, generalized anxiety disorder (GAD), a phobia disorder, binge eating disorder, body dysmorphic disorder, an alcohol or drug abuse or dependence disorder, a substance use disorder, substance-induced mood disorder, a mood disorder related to another health condition, a disruptive behavior disorder, an eating disorder, an impulse control disorder, obsessive compulsive disorder (OCD), attention deficit hyperactivity disorder (ADHD), prolonged grief disorder, a personality disorder, autism, autism spectrum disorder, social anxiety in autism, an attachment disorder, and a dissociative disorder.

5. The composition or kit of parts of claim 1 , comprising between about 50 mg and about 300 mg, between about 75 mg and about 200 mg, between about 100 mg and about 150 mg, about 125 mg, or about 175 mg of CX157, or a pharmaceutically acceptable salt thereof.

6. The composition or kit of parts of claim 5 , comprising about 175 mg of CX157, or a pharmaceutically acceptable salt thereof.

7. The composition or kit of parts of claim 1 , comprising between about 1 mg and about 300 mg of DMT, or a pharmaceutically acceptable salt thereof.

8. The composition or kit of parts of claim 7 , comprising between about 1 mg and about 10 mg of DMT, or a pharmaceutically acceptable salt thereof.

9. The composition or kit of parts of claim 7 , comprising between about 10 mg and about 60 mg of DMT, or a pharmaceutically acceptable salt thereof.

10. The composition or kit of parts of claim 7 , comprising between about 60 mg and about 250 mg of DMT, or a pharmaceutically acceptable salt thereof.

11. The composition or kit of parts of claim 1 , wherein the CX157 or the DMT is formulated for modified release.

12. The composition or kit of parts of claim 1 , further comprising a pharmaceutically acceptable carrier, diluent, or excipient.

13. The composition of claim 12 , wherein the pharmaceutically acceptable carrier, diluent, or excipient comprises copovidone, microcrystalline cellulose, hypromellose, colloidal silicon dioxide, or magnesium stearate.

14. The method of claim 2 , wherein the amount administered to the subject of CX157, or a pharmaceutically acceptable salt thereof, is between about 50 mg and about 300 mg, between about 75 mg and about 200 mg, between about 100 mg and about 150 mg, about 125 mg, or about 175 mg.

15. The method of claim 14 , wherein the amount administered to the subject of CX157, or a pharmaceutically acceptable salt thereof, is about 175 mg.

16. The method of claim 2 , wherein the amount administered to the subject of DMT, or a pharmaceutically acceptable salt thereof, is between about 0.05 mg/kg and about 3 mg/kg.

17. The method of claim 16 , wherein the amount administered to the subject of DMT, or a pharmaceutically acceptable salt thereof, is between about 0.05 mg/kg and about 0.10 mg/kg.

18. The method of claim 16 , wherein the amount administered to the subject of DMT, or a pharmaceutically acceptable salt thereof, is between about 0.30 mg/kg and about 0.60 mg/kg.

19. The method of claim 16 , wherein the amount administered to the subject of DMT, or a pharmaceutically acceptable salt thereof, is between about 0.60 mg/kg and about 3 mg/kg.

Assignments (1)

Continuity (4)

References Cited (156)