IP Library Granted Patent US 11,253,500
Granted Patent B2
US 11,253,500 · App. 16/611,908 · Granted Feb 22, 2022

Sanfetrinem or a salt or ester thereof for use in treating mycobacterial infection

Inventors: David Barros Aguirre (Madrid, ES); Robert H. Bates (Madrid, ES); Ruben Gonzalez Del Rio (Madrid, ES); Alfonso Mendoza Losana (Madrid, ES); Santiago Ramón García (Saragossa, ES)
Assignee: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
A61K31/407A61K31/424A61K31/43A61K45/06A61P31/06
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Quick Facts
Patent No.
US 11,253,500
App. No.
16/611,908
Granted
Feb 22, 2022
Kind
B2
Abstract

The present invention relates to or a pharmaceutically acceptable salt or ester prodrug thereof for use in the treatment of a mycobacterial infection or disease resulting from a mycobacterial infection, such as tuberculosis.

Claims (27)

1. A method for the treatment of a disease resulting from a mycobacterial infection in a human in need thereof, comprising administering to said human a therapeutically effective amount of a compound which is

or a pharmaceutically acceptable salt thereof.

2. The method according to claim 1 , wherein the disease is tuberculosis.

3. A method for the treatment of a disease resulting from a mycobacterial infection in a human in need thereof, comprising administering to said human a therapeutically effective amount of a compound which is

or a pharmaceutically acceptable salt thereof.

4. The method according to claim 1 , wherein the compound or salt thereof is a sodium salt of compound which is

5. A method of treating tuberculosis in a human in need thereof, comprising administering to said human a composition comprising

(a) the compound which is

or a pharmaceutically acceptable salt or ester prodrug thereof, wherein the ester prodrug is

or a pharmaceutically acceptable salt thereof, and

(b) a pharmaceutically acceptable excipient.

6. A method of treating tuberculosis in a human in need thereof, comprising administering to said human a combination comprising

(a) the compound which is

or a pharmaceutically acceptable salt or ester prodrug thereof, wherein the ester prodrug is

or a pharmaceutically acceptable salt thereof, and

(b) a further anti-tuberculosis agent.

7. The method according to claim 6 , wherein the further anti-tuberculosis agent is selected from isoniazid, rifampin, pyrazinamide, ethambutol, moxifloxacin, rifapentine, clofazimine, ethionamide, prothionamide, isoxyl, thiacetazone, rifabutin, a diarylquinoline such as bedaquiline (TMC207) or TBAJ-587, nitroimidazo-oxazine PA-824, delamanid (OPC-67683), an oxazolidinone, linezolid, tedizolid, radezolid, sutezolid (PNU-100480), posizolid (AZD-5847), TBI-223, EMB analogue SQ109, OPC-167832, GSK3036656 (GSK070), GSK2556286, GSK3211830, a benzothiazinone, BTZ043, PBTZ169, an azaindole, TBA-7371, a dinitrobenzamide, a beta-lactam, meropenem, faropenem, ertapenem, tebipenem, beta-lactam combinations, and AUGMENTIN (amoxicillin-clavulanate).

8. The method according to claim 6 , wherein the further anti-tuberculosis agent is AUGMENTIN (amoxicillin-clavulanate).

9. The method according to claim 6 , further comprising an antiretroviral agent.

10. The method according to claim 9 , wherein the antiretroviral agent is selected from zidovudine, didanosine, lamivudine, zalcitabine, abacavir, stavudine, adefovir, adefovir dipivoxil, fozivudine, todoxil, emtricitabine, alovudine, amdoxovir, elvucitabine, nevirapine, delavirdine, efavirenz, loviride, immunocal, oltipraz, capravirine, lersivirine, GSK2248761, TMC-278, TMC-125, etravirine, saquinavir, ritonavir, indinavir, nelfinavir, amprenavir, fosamprenavir, brecanavir, darunavir, atazanavir, tipranavir, palinavir, lasinavir, enfuvirtide, T-20, T-1249, PRO-542, PRO-140, TNX-355, BMS-806, BMS-663068, BMS-626529, 5-Helix, raltegravir, elvitegravir, GSK1349572, GSK1265744, vicriviroc (Sch-C), Sch-D, TAK779, maraviroc, TAK449, didanosine, tenofovir, lopinavir, and darunavir.

11. A method for the treatment of a disease resulting from a mycobacterial infection in a human in need thereof, comprising administering to said human (a) the compound

or a pharmaceutically acceptable salt or ester prodrug thereof; wherein the ester prodrug is

or a pharmaceutically acceptable salt thereof, and

(b) a β-lactamase inhibitor.

12. The method of claim 11 wherein the disease is tuberculosis.

13. The method of claim 11 wherein the β-lactamase inhibitor is clavulanate or clavulanic acid.

14. The method according to claim 3 , wherein the disease is tuberculosis.

Assignments (4)
CHANGE OF ADDRESS Recorded Oct 8, 2025
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 073032/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2019
From: BARROS AGUIRRE, DAVID; BATES, ROBERT H.; GONZALEZ DEL RIO, RUBEN; MENDOZA LOSANA, ALFONSO
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 050955/0715 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2019
From: RAMÓN GARCÍA, SANTIAGO
To: THE UNIVERSITY OF BRITISH COLOMBIA
Reel/Frame 050955/0902 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2019
From: THE UNIVERSITY OF BRITISH COLOMBIA; GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 050956/0016 →
Priority Claims (1)
EP 17382255 · May 8, 2017 · regional
Continuity (1)
Related Publication 20200289462A1 · Sep 17, 2020