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Details for Patent: 9,393,237

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Details for Patent: 9,393,237

Title:Method of treating thermoregulatory dysfunction with paroxetine
Abstract: The present invention relates to a method for treating a patient suffering from a thermoregulatory dysfunction, especially hot flashes and flushes associated with hormonal changes due to naturally occurring menopause (whether male or female) or due to chemically or surgically induced menopause. The method is also applicable to treating the hot flashes, hot flushes, or night sweats associated with disease states that disrupt normal hormonal regulation of body temperature.
Inventor(s): Richards; Patricia Allison Tewes (Bradenton, FL)
Assignee: NOVEN THERAPEUTICS, LLC (Miami, FL)
Filing Date:Dec 19, 2014
Application Number:14/577,227
Claims:1. A method for treating a female patient suffering from thermoregulatory dysfunction associated with menopause, consisting of administering a dosage form of paroxetine to said patient in an amount, based on the paroxetine moiety, of 7.5 mg/day.

2. The method of claim 1, wherein said thermoregulatory dysfunction is a condition selected from the group consisting of hot flashes, hot flushes, night sweats, and combinations thereof.

3. The method of claim 1, wherein said dosage form comprises paroxetine free base.

4. The method of claim 1, wherein said dosage form comprises a pharmaceutically acceptable salt of paroxetine.

5. The method of claim 1, wherein said dosage form comprises a pharmaceutically acceptable salt of paroxetine selected from the group consisting of hydrohalides, sulfates, phosphates, oxalate, tosylate, pamoate, citrate, carbonate, bicarbonate, maleate, malate, and fumarate.

6. The method of claim 1, wherein said dosage form comprises a pharmaceutically acceptable salt of paroxetine selected from the group consisting of hydrochloride, hydrobromide, and hydroiodide, and combinations of two or more thereof.

7. The method of claim 1, wherein said dosage form comprises paroxetine hydrochloride.

8. The method of claim 1, wherein said dosage form comprises a pharmaceutically acceptable salt of paroxetine selected from the group consisting of sulfate and bisulfate, and combinations thereof.

9. The method of claim 1, wherein said dosage form comprises paroxetine mesylate.

10. The method of claim 1, wherein said dosage form comprises a pharmaceutically acceptable salt of paroxetine selected from the group consisting of mono, di, and tri basic phosphates, and combinations of two or more thereof.

11. The method of claim 1, wherein said dosage form comprises paroxetine or a pharmaceutically acceptable salt thereof in anhydrate, hydrate, or solvate form, or a combination of two or more thereof.

12. The method of claim 1, wherein said dosage form comprises paroxetine or a pharmaceutically acceptable salt thereof in a crystalline or amorphous form, or a combination thereof.

13. The method of claim 1, wherein said dosage form comprises paroxetine or a pharmaceutically acceptable salt thereof in a crystalline form.

14. The method of claim 1, wherein said dosage form comprises paroxetine or a pharmaceutically acceptable salt thereof in an amorphous form.
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