Compositions and methods for treating central nervous system (cns) disorders and mood disorders
US-2018319843-A1 · Nov 8, 2018 · US
US10653743B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10653743-B2 |
| Application number | US-201615768267-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 17, 2016 |
| Priority date | Oct 15, 2015 |
| Publication date | May 19, 2020 |
| Grant date | May 19, 2020 |
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Compositions and methods for treating a depressive disorder or an anxiety disorder in a subject in need of such treatment are described. A therapeutically effective amount of a composition comprising compound PG-20N in a pharmaceutically acceptable carrier is described. According to another embodiment, the subject disclosure features method of treating a depressive disorder or an anxiety disorder in a subject in need of such treatment. The method may comprise administering to the subject a therapeutically effective amount of a composition comprising PG-20N.
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What is claimed is: 1. A method of treating a depressive disorder or an anxiety disorder in a subject in need of such treatment, said method comprising administering to the subject a therapeutically effective amount of a composition comprising: in a pharmaceutically acceptable carrier. 2. The method of claim 1 , wherein the subject is a mammal. 3. The method of claim 2 , wherein the mammal is a human. 4. The method of claim 1 , wherein the composition is administered in a dosage of about 0.001 mg/kg to 100 mg/kg of body weight. 5. The method of claim 1 , wherein the composition is administered at least once daily, at least once every other day, or at least once weekly. 6. The method of claim 1 , wherein the composition is administered intravenously, transdermally, or orally. 7. A method of treating a depressive disorder in a subject in need of such treatment, said method comprising administering to the subject a therapeutically effective amount of a composition comprising: in a pharmaceutically acceptable carrier, wherein administration of the composition treats the depressive disorder in the subject such that clinical improvement is observed in about 1 to 14 days. 8. The method of claim 7 , wherein the subject is a mammal. 9. The method of claim 8 , wherein the mammal is a human. 10. The method of claim 7 , wherein the composition is administered in a dosage of about 0.001 mg/kg to 100 mg/kg of body weight. 11. The method of claim 7 , wherein the composition is administered at least once daily, at least once every other day, or at least once weekly. 12. The method of claim 7 , wherein the composition is administered intravenously, transdermally, or orally.
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