US2024000815A1PendingUtilityA1
Deuterated derivatives of psilocybin and uses thereof
Est. expiryOct 8, 2040(~14.2 yrs left)· nominal 20-yr term from priority
Inventors:Bradford C. Sippy
A61K 31/675A61K 31/4045
78
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Claims
Abstract
Provided herein are pharmaceutical compositions comprising deuterated derivatives of psilocybin. The provided compositions may be useful for treating and/or preventing various diseases and conditions, such as mood or psychiatric disorders.
Claims
exact text as granted — not AI-modified1 - 20 . (canceled)
21 . A pharmaceutical composition comprising a deuterated compound of structure:
or a pharmaceutically acceptable salt, prodrug, hydrate, or solvate thereof;
wherein the pharmaceutical composition comprises about 0.5 mg to 500 mg of the compound.
22 . The composition of claim 21 , wherein the composition further comprises a pharmaceutically acceptable carrier.
23 . The composition of claim 22 , wherein the composition is suitable for oral administration.
24 . The composition of claim 22 , wherein the composition is suitable for intravenous (IV) administration.
25 . The composition of claim 23 , wherein the composition is a solid dose composition.
26 . The composition of claim 25 , wherein the solid dose composition is a tablet, capsule, granule, powder, sachet, or chewable.
27 . The composition of claim 21 , wherein the composition comprises about 0.5 mg to about 250 mg of the deuterated compound, or a pharmaceutically acceptable salt thereof.
28 . The composition of claim 27 , wherein the composition comprises about 0.5 mg to about mg of the deuterated compound, or a pharmaceutically acceptable salt thereof.
29 . The composition of claim 28 , wherein the composition comprises about 10 mg to about mg of the deuterated compound, or a pharmaceutically acceptable salt thereof.
30 . The composition of claim 22 , wherein the composition comprises about 0.01 mg/ml to about 50 mg/ml of the deuterated compound, or a pharmaceutically acceptable salt thereof.
31 . A method of treating a neurological or psychiatric disorder in a subject in need thereof, the method comprising administering an effective amount of a pharmaceutical composition comprising a deuterated compound of structure:
or a pharmaceutically acceptable salt, prodrug, hydrate, or solvate thereof.
32 . The method of claim 31 , wherein the disorder is a psychiatric disorder.
33 . The method of claim 32 , wherein the psychiatric disorder is a depressive disorder or an eating disorder.
34 . The method of claim 33 , wherein the depressive disorder is major depressive disorder or treatment-resistant depression.
35 . The method of claim 31 , wherein the disorder is a neurological disorder.
36 . The method of claim 35 , wherein the neurological disorder is a pain disorder.
37 . The method of claim 31 , wherein the composition comprises the deuterated compound, or a pharmaceutically acceptable salt thereof.
38 . The method of claim 37 , wherein the composition comprises about 0.5 mg to about 50 mg of the deuterated compound, or a pharmaceutically acceptable salt thereof.
39 . The method of claim 37 , wherein the composition comprises about 10 mg to about 50 mg of the deuterated compound, or a pharmaceutically acceptable salt thereof.
40 . The method of claim 31 , wherein the composition is administered orally.Cited by (0)
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