US2014057923A1PendingUtilityA1
Treating Sexual Desire Disorders with Flibanserin
Assignee: SPROUT PHARMACEUTICALS INCPriority: Oct 20, 2001Filed: Jun 18, 2013Published: Feb 27, 2014
Est. expiryOct 20, 2021(expired)· nominal 20-yr term from priority
A61P 43/00A61P 25/24A61P 25/18A61P 25/22A61P 15/10A61P 15/00A61K 31/496
64
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The invention relates to the use of flibanserin, or a pharmaceutically acceptable acid addition salt thereof, for the treatment of disorders of sexual desire.
Claims
exact text as granted — not AI-modified1 . A method of treating decreased sexual desire in a patient, comprising administering a therapeutically effective amount of flibanserin or a pharmaceutically acceptable acid addition salt thereof to the patient to treat decreased sexual desire.
2 . The method according to claim 1 , wherein the patient is female.
3 . The method according to claim 1 , wherein the patient is male.
4 . The method according to claim 1 , wherein the amount administered is between about 0.1 mg and 400 mg per day of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
5 . The method according to claim 1 , wherein the amount administered is between about 1 mg and 300 mg per day of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
6 . The method according to claim 1 , wherein the amount administered is in a dosage unit containing between about 0.01 mg and 100 mg of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
7 . The method according to claim 1 , wherein the amount administered is in a dosage unit containing between about 0.1 mg and 50 mg of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
8 . A method of treating absent sexual desire in a patient, comprising administering a therapeutically effective amount of flibanserin or a pharmaceutically acceptable acid addition salt thereof to the patient to treat decreased sexual desire.
9 . The method according to claim 8 , wherein the patient is female.
10 . The method according to claim 8 , wherein the patient is male.
11 . The method according to claim 8 , wherein the amount administered is between about 2 mg and 200 mg per day of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
12 . The method according to claim 8 , wherein the amount administered is between about 0.1 mg and 100 mg per day of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
13 . The method according to claim 8 , wherein the amount administered is in a dosage unit containing about 150 mg of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
14 . A method of treating inhibited sexual desire in a patient, comprising administering a therapeutically effective amount of flibanserin or a pharmaceutically acceptable acid addition salt thereof to the patient to treat decreased sexual desire.
15 . The method according to claim 14 , wherein the patient is female.
16 . The method according to claim 14 , wherein the patient is male.
17 . The method according to claim 14 , wherein the amount administered is between about 0.1 mg and 400 mg per day of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
18 . The method according to claim 14 , wherein the amount administered is in a dosage unit containing about 100 mg of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
19 . The method according to claim 14 , wherein the amount administered is in a dosage unit containing about 80 mg of flibanserin or a pharmaceutically acceptable acid addition salt thereof.
20 . The method according to claim 14 , wherein the amount administered is in a dosage unit containing about 50 mg of flibanserin or a pharmaceutically acceptable acid addition salt thereof.Join the waitlist — get patent alerts
Track US2014057923A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.