Therapeutic compositions comprising deuterated or partially deuterated N,N-dimethyltryptamine compounds
The present invention relates to compositions comprising N,N-dimethyltryptamine, deuterated N,N-dimethyltryptamine and/or partially deuterated N,N-dimethyltryptamine. In particular, the present invention relates to compositions comprising a combination of N,N-dimethyltryptamine and 2% or more by weight of one or more deuterated N,N-dimethyltryptamine compound selected from α,α-dideutero-N,N-dimethyltryptamine and α,α,β,β-tetradeutero-N,N-dimethyltryptamine. Additional and alternative compositions of the present invention comprise a combination of N,N-dimethyltryptamine and 2% or more by weight of one or more partially deuterated N,N-dimethyltryptamine compound selected from α,β,β-trideutero-N,N-dimethyltryptamine, α,β-dideutero-N,N-dimethyltryptamine, and α-deutero-N,N-dimethyltryptamine. Methods of synthesising compositions of the present invention, and methods of use of presently described compositions in treating psychiatric or psychocognitive disorders, such as major depressive disorder, are also provided.
1. A composition comprising:
a) α-protio, α-deutero-N,N-dimethyltryptamine, or a pharmaceutically acceptable salt thereof;
b) α,α-dideutero-N,N-dimethyltryptamine, or a pharmaceutically acceptable salt thereof; and
c) N,N-dimethyltryptamine, or a pharmaceutically acceptable salt thereof,
wherein the composition comprises 50% or more by weight of α,α-dideutero-N,N-dimethyltryptamine, or a pharmaceutically acceptable salt thereof or α-protio, α-deutero-N,N-dimethyltryptamine, or a pharmaceutically acceptable salt thereof.
2. The composition of claim 1 comprising 60% or more by weight of a, α-dideutero-N,N-dimethyltryptamine or a pharmaceutically acceptable salt thereof or α-protio, α-deutero-N,N-dimethyltryptamine or a pharmaceutically acceptable salt thereof.
3. The composition of claim 1 comprising 50% or more by weight of α,α-dideutero-N,N-dimethyltryptamine or a pharmaceutically acceptable salt thereof.
4. The composition of claim 1 having a purity of greater than or equal to 99% by HPLC.
5. The composition of claim 4 having a purity of greater than or equal to 99.9% by HPLC.
6. The composition of claim 1 , wherein α,α-dideutero-N,N-dimethyltryptamine, α-protio, α-deutero-N,N-dimethyltryptamine and N,N-dimethyltryptamine are in the form of a pharmaceutically acceptable salt.
7. The composition of claim 1 , wherein the pharmaceutically acceptable salt is a fumarate salt.
8. The composition of claim 2 , wherein the pharmaceutically acceptable salt is a fumarate salt.
9. The composition of claim 3 , wherein the pharmaceutically acceptable salt is a fumarate salt.
10. The composition of claim 4 , wherein the pharmaceutically acceptable salt is a fumarate salt.
11. The composition of claim 5 , wherein the pharmaceutically acceptable salt is a fumarate salt.
12. The composition of claim 6 , wherein the pharmaceutically acceptable salt is a fumarate salt.
13. A pharmaceutical composition comprising a composition as defined in claim 1 in combination with a pharmaceutically acceptable excipient.
14. A pharmaceutical composition comprising a composition as defined in claim 2 in combination with a pharmaceutically acceptable excipient.
15. A pharmaceutical composition comprising a composition as defined in claim 3 in combination with a pharmaceutically acceptable excipient.
16. A pharmaceutical composition comprising a composition as defined in claim 4 in combination with a pharmaceutically acceptable excipient.
17. A pharmaceutical composition comprising a composition as defined in claim 5 in combination with a pharmaceutically acceptable excipient.
18. A pharmaceutical composition comprising a composition as defined in claim 6 in combination with a pharmaceutically acceptable excipient.
19. A pharmaceutical composition comprising a composition as defined in claim 7 in combination with a pharmaceutically acceptable excipient.
20. A pharmaceutical composition comprising a composition as defined in claim 8 in combination with a pharmaceutically acceptable excipient.