IP Library Patent Application 14333966
Patent Application
App. No. 14/333,966

CEPHALOSPORIN COMPOUND

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Quick Facts
Patent No.
US None
App. No.
14/333,966
Abstract

The cephalosporin compound of formula (I) is disclosed, which exhibits antibiotic activity against Gram-negative (e.g., Pseudomonas aeruginosa ) and Gram-positive (e.g., methicillin-resistant Staphylococcus aureus ) bacteria. Methods of manufacturing the compound of formula (I), and uses of the compound in the preparation of pharmaceutical compositions and antibacterial applications are also disclosed.

Claims (18)

1 - 3 . (canceled)

4 . A method for treating an infectious disease comprising administering to a subject in need thereof a therapeutically effective amount of a composition comprising the compound of Formula (I):

or a pharmaceutically acceptable salt thereof.

5 - 9 . (canceled)

10 . The method of claim 4 , wherein the infectious diseases is caused by a Gram-negative bacteria.

11 . The method of claim 10 , wherein the Gram-negative bacteria is Pseudomonas aeruginosa.

12 . The method of claim 4 , wherein the subject has hospital acquired pneumonia (HAP).

13 . The method of claim 4 , wherein the subject has ventilator acquired pneumonia (VAP).

14 . A method of treating an infection caused by Pseudomonas aeruginosa, comprising parenterally administering to a patient in need thereof a pharmaceutical composition comprising a carrier and a therapeutically effective amount of a compound of Formula (I):

a physiologically hydrolyzable ester thereof, a solvate thereof, or a pharmacologically acceptable salt thereof.

15 . The method of claim 14 , wherein the therapeutically effective amount is effective against a Pseudomonas aeruginosa bacteria with a minimum inhibitory concentration (MIC) of not more than about 4 micrograms/mL.

16 . The method of claim 15 , wherein the minimum inhibitory concentration (MIC) is not more than about 2 micrograms/mL.

17 . The method of claim 15 , wherein the minimum inhibitory concentration (MIC) is not more than about 1 microgram/mL.

18 . The method of claim 15 , wherein the subject has hospital acquired pneumonia (HAP).

19 . The method of claim 15 , wherein the subject has ventilator acquired pneumonia (VAP).

20 . A method of making the compound of Formula (I) comprising the step of reacting intermediate compound 6:

with an intermediate compound 12:

to produce the compound of Formula (I):

Assignments (3)
NUNC PRO TUNC ASSIGNMENT Recorded Aug 6, 2015
From: CUBIST PHARMACEUTICALS LLC
To: MERCK SHARP & DOHME CORP.
Reel/Frame 036268/0626 →
CHANGE OF NAME Recorded Aug 5, 2015
From: CUBIST PHARMACEUTICALS, INC.
To: CUBIST PHARMACEUTICALS LLC
Reel/Frame 036283/0189 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2014
From: HE, YONG; GU, YU GUI; YE, NING
To: CUBIST PHARMACEUTICALS, INC.
Reel/Frame 033360/0766 →