US2016199379A1PendingUtilityA1
Antiviral therapy
Est. expiryJan 27, 2030(~3.5 yrs left)· nominal 20-yr term from priority
Inventors:Mark Richard Underwood
A61P 31/12A61P 37/04A61P 31/00A61P 31/18A61P 43/00A61K 9/0014A61K 9/0019A61K 9/0053A61K 31/505A61K 31/52A61K 31/5365A61K 2121/00A61K 31/675A61K 31/536A61K 31/513A61K 45/06A61K 31/4985A61K 2300/00
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Claims
Abstract
The present invention relates to combinations of compounds comprising HIV integrase inhibitors and other therapeutic agents. Such combinations are useful in the inhibition of HIV replication, the prevention and/or treatment of infection by HIV, and in the treatment of AIDS and/or ARC
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treating HIV infection by administering to a subject the compound of formula (I)
or a pharmaceutically acceptable salt thereof, with a therapeutic agent that is the active ingredient tenofavir in the subject.
2 . The method of claim 1 wherein the therapeutic agent is a fumaric acid salt.
3 . The method of claim 2 further comprising administering a nucleoside reverse transcriptase inhibitor.
4 . The method of claim 1 , wherein the subject is administered a composition comprising 20-300 mg of the compound of formula (I) or an equivalent dose of a pharmaceutically acceptable salt thereof, 20-300 mg of a fumaric acid salt of a therapeutic agent that is the active ingredient tenofavir in the subject, and 20-300 mg of a nucleoside reverse transcriptase inhibitor.
5 . A method according to claim 4 wherein the composition is given once a day.
6 . A method according to claim 4 wherein the composition is in unit dosage form.
7 . A pharmaceutical composition comprising a compound of formula (I)
or a pharmaceutically acceptable salt thereof, with a therapeutic agent that is the active ingredient tenofavir in the subject.
8 . The pharmaceutical composition according to claim 7 wherein the the therapeutic agent is a fumaric acid salt.
9 . The pharmaceutical composition according to claim 7 further comprising a nucleoside reverse transcriptase inhibitor.
10 . The pharmaceutical composition according to claim 7 in a unit dosage form.
11 . The pharmaceutical composition according to claim 7 comprising 20-300 mg of the compound of formula (I) or an equivalent dose of a pharmaceutically acceptable salt thereof, 20-300 mg of a fumaric acid salt of a therapeutic agent that is the active ingredient tenofavir in the subject, and 20-300 mg of a nucleoside reverse transcriptase inhibitor.
12 . The pharmaceutical composition according to claim 11 in unit dosage form.
13 . A combination comprising as active ingredients, the compound of formula (I),
or a pharmaceutically acceptable salt thereof, tenofovir, and a nucleoside reverse transcriptase inhibitor.
14 . The combination of claim 13 in unit dosage form.
15 . A combination comprising as active ingredients 20-300 mg of the compound of formula (I),
or a pharmaceutically acceptable salt thereof, 20-300 of tenofovir, and 20-300 mg of a nucleoside reverse transcriptase inhibitor.
16 . The combination of claim 15 in unit dosage form.Join the waitlist — get patent alerts
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