US2010093762A1PendingUtilityA1
Methods for treating or preventing symptoms of hormonal variations
Est. expiryDec 13, 2026(~0.4 yrs left)· nominal 20-yr term from priority
Inventors:Hung-Ming Wu
A61P 5/24A61P 43/00A61P 9/00A61P 5/00A61P 25/22A61P 25/06A61P 25/02A61P 25/20A61P 3/00A61K 31/519A61K 31/551A61K 31/496A61K 31/5513A61P 1/08A61K 31/554A61K 31/38A61P 15/12A61K 31/505
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Claims
Abstract
A method for treating or preventing symptoms of hormonal variation includes administering an effective amount of a receptor antagonist to a subject having one or more symptoms of hormonal variations, wherein the receptor antagonist binds to at least one selected from the group consisting of a serotonin type 2A (5-HT 2A ) and a dopamine type 2 (D 2 ) receptors.
Claims
exact text as granted — not AI-modified1 . A method for treating or preventing symptoms of hormonal variation, comprising: administering an effective amount of a receptor antagonist to a subject having one or more symptoms of hormonal variations, wherein the receptor antagonist binds to at least one selected from the group consisting of a serotonin type 2A (5-HT 2A ) receptor and a dopamine type 2 (D 2 ) receptor, and wherein the symptoms of hormonal variation are associated with perimenopause or postmenopause.
2 . The method of claim 1 , wherein the symptoms of hormonal variation comprises at least one selected from hot flashes, dizziness, nausea, headaches, palpitations, profuse sweating, and night sweats.
3 . The method of claim 1 , wherein the receptor antagonist is at least one selected from risperidone, 9-hydroxyrisperidone, quetiapine, clozapine, otanzapine, aripiprazole, ziprasidone, and zotepine.
4 . The method of claim 1 , wherein the receptor antagonist is risperidone.
5 . The method of claim 4 , wherein the effective amount of risperidone is from 0.1 to 50 mg per day for an adult patient.
6 . The method of claim 4 , wherein the effective amount of risperidone is from 0.1 to 20 mg per day for an adult patient.
7 . The method of claim 4 , wherein the effective amount of risperidone is from 0.1 to 6 mg per day for an adult patient.
8 . The method of claim 4 , wherein the effective amount of risperidone is from 0.1 to 2 mg per day for an adult patient.
9 . The method of claim 1 , wherein the receptor antagonist is 9-hydroxyrisperidone.
10 . The method of claim 11 , wherein the pharmaceutically acceptable formulation is at least one selected from, oral formulation, injection, inhalation, and transdermal patch.
11 . The method of claim 1 , wherein the effective amount of the receptor antagonist is administered by using a pharmaceutically acceptable formulation.
12 . The method of claim 9 , wherein the effective amount of 9-hydroxyrisperidone is from 0.1 to 50 mg per day for an adult patient.
13 . The method of claim 9 , wherein the effective amount of 9-hydroxyrisperidone is from 0.1 to 20 mg per day for an adult patient.
14 . The method of claim 9 , wherein the effective amount of 9-hydroxyrisperidone is from 0.1 to 6 mg per day for an adult patient.
15 . The method of claim 9 , wherein the effective amount of 9-hydroxyrisperidone is from 0.1 to 2 mg per day for an adult patient.
16 . The method of claim 9 , wherein the effective amount of the receptor antagonist is administered by using a pharmaceutically acceptable formulation.
17 . The method of claim 16 , wherein the pharmaceutically acceptable formulation is at least one selected from oral formulation, injection, inhalation, and transdermal patch.
18 . The method of claim 1 , wherein the receptor antagonists is a mixture of risperidone and 9-hydroxyrisperidone.Join the waitlist — get patent alerts
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