US2004229881A1PendingUtilityA1
Methods of use of antimicrobial compounds against pathogenic mycoplasma bacteria
Est. expiryJun 29, 2019(expired)· nominal 20-yr term from priority
A61K 31/47
51
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Claims
Abstract
This invention relates, in part, to newly identified methods of using quinolone antibiotics, particularly a gemifloxacin compound against certain pathogenic bacteria, including Mycoplasma bacteria, such as Mycoplasma pneumoniae.
Claims
exact text as granted — not AI-modified1 . (Canceled)
2 . (Canceled)
3 . A method of treating or preventing a bacterial infection by pathogenic Mycoplasma bacteria comprising the step of administering an antibacterially effective amount of a composition comprising a gemifloxacin compound, or an antibacterially effective derivative thereof, to a mammal suspected of having or being at risk of having an infection with pathogenic Mycoplasma bacteria.
4 - 7 . (Canceled)
8 . The method of claim 3 wherein said mammal is a human.
9 - 11 . (Canceled)
12 . The method of claim 3 wherein said pathogenic Mycoplasma bacteria is a member of the genus Mycoplasma.
13 . The method of claim 12 wherein said bacteria is selected from the group consisting of Mycoplasma hominis and Mycoplasma fermentans.
14 . The method of claim 12 wherein said bacteria is selected from the group consisting of Mycoplasma pneumoniae, Mycoplasma genitalium , and Mycoplasma penetrans.
15 . The method of claim 3 wherein said bacteria is a member of the genus Ureaplasma.
16 . The method of claim 15 wherein said bacteria is Ureaplasma urealyticum.
17 . The method according to claim 3 wherein the gemifloxacin compound is gemifloxacin or a pharmaceutically acceptable salt thereof.
18 . The method according to claim 17 wherein the gemifloxacin compound is gemifloxacin mesylate or a hydrate thereof.
19 . The method according to claim 18 wherein the gemifloxacin compound is gemifloxacin mesylate sesquihydrate.
20 . The method according to claim 12 wherein the gemifloxacin compound is gemifloxacin or a pharmaceutically acceptable salt thereof.
21 . The method according to claim 20 wherein the gemifloxacin compound is gemifloxacin mesylate or a hydrate thereof.
22 . The method according to claim 21 wherein the gemifloxacin compound is gemifloxacin mesylate sesquihydrate.
23 . The method according to claim 13 wherein the gemifloxacin compound is gemifloxacin or a pharmaceutically acceptable salt thereof.
24 . The method according to claim 23 wherein the gemifloxacin compound is gemifloxacin mesylate or a hydrate thereof.
25 . The method according to claim 24 wherein the gemifloxacin compound is gemifloxacin mesylate sesquihydrate.
26 . The method according to claim 14 wherein the gemifloxacin compound is gemifloxacin or a pharmaceutically acceptable salt thereof.
27 . The method according to claim 26 wherein the gemifloxacin compound is gemifloxacin mesylate or a hydrate thereof.
28 . The method according to claim 27 wherein the gemifloxacin compound is gemifloxacin mesylate sesquihydrate.
29 . The method according to claim 15 wherein the gemifloxacin compound is gemifloxacin or a pharmaceutically acceptable salt thereof.
30 . The method according to claim 29 wherein the gemifloxacin compound is gemifloxacin mesylate or a hydrate thereof.
31 . The method according to claim 30 wherein the gemifloxacin compound is gemifloxacin mesylate sesquihydrate.
32 . The method according to claim 16 wherein the gemifloxacin compound is gemifloxacin or a pharmaceutically acceptable salt thereof.
33 . The method according to claim 32 wherein the gemifloxacin compound is gemifloxacin mesylate or a hydrate thereof.
34 . The method according to claim 33 wherein the gemifloxacin compound is gemifloxacin mesylate sesquihydrate.Join the waitlist — get patent alerts
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