US2018042918A1PendingUtilityA1
Respiratory infection treating agent
Est. expiryMar 13, 2035(~8.6 yrs left)· nominal 20-yr term from priority
A61P 31/04A61P 11/00A61P 11/04A61K 31/4709Y02A50/30
37
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Claims
Abstract
[Problem] The present invention pertains to a safer and more effective respiratory infection treating agent. [Solution] A respiratory infection treating agent containing, as an active ingredient, 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof.
Claims
exact text as granted — not AI-modified1 . A respiratory infection treating agent comprising, as an active ingredient, 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof.
2 . The treating agent according to claim 1 , wherein the respiratory infection treating agent is a respiratory infection treating agent for human.
3 . The treating agent according to claim 1 , wherein the respiratory infection is one or two or more infections selected from the group consisting of pharyngitis, laryngitis, tonsillitis, acute bronchitis, pneumonia, and secondary infections of chronic respiratory diseases.
4 . The treating agent according to claim 1 , wherein pathogenic bacteria causing the respiratory infection are one or two or more types of bacteria selected from the group consisting of bacteria belonging to Staphylococcus sp., bacteria belonging to Streptococcus sp., Moraxella catarrhalis , bacteria belonging to Klebsiella sp., Haemophilus influenzae , and Escherichia coli.
5 . The treating agent according to claim 1 , wherein pathogenic bacteria causing the respiratory infection are one or two or more types of bacteria belonging to any of Streptococcus sp. and Staphylococcus sp.
6 . The treating agent according to claim 1 , wherein pathogenic bacteria causing the respiratory infection have drug resistance.
7 . The treating agent according to claim 1 , wherein a dose of 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof per day is 10 mg or more and 250 mg or less.
8 . A treating agent for an infection which is one or two or more selected from the group consisting of pharyngitis, laryngitis, tonsillitis, acute bronchitis, pneumonia, secondary infections of chronic respiratory diseases, sinusitis, and tympanitis, and in which pathogenic bacteria are Streptococcus pneumoniae , the treating agent comprising, as an active ingredient, 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof.
9 . The treating agent for an infection according to claim 8 , wherein a dose of 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof per day is 10 mg or more and 250 mg or less.
10 . The treating agent according to claim 1 , wherein a dose of 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof per day is 75 mg or two times the amount.
11 . A treating agent for an infection which is one or two or more selected from the group consisting of pharyngitis, laryngitis, tonsillitis, acute bronchitis, pneumonia, secondary infections of chronic respiratory diseases, sinusitis, and tympanitis, the treating agent comprising 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof, wherein a dose of the compound per day is 75 mg or two times the amount.
12 . The treating agent according to claim 1 , wherein a maximum plasma concentration of 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof after administration of the treating agent to human with a respiratory infection is 3 μg/mL or less.
13 . An infection treating agent containing 7-[(3S,4S)-3-{(cyclopropylamino)methyl}-4-fluoropyrrolidine-1-yl]-6-fluoro-1-(2-fluoroethyl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid or a pharmaceutically acceptable salt thereof, wherein a tissue distribution ratio of the compound into an alveolar epithelial lining fluid 1 hour after administration to human is 10 or more.Join the waitlist — get patent alerts
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