IP Library Granted Patent US 9,901,560
Granted Patent B2
US 9,901,560 · App. 15/379,063 · Granted Feb 27, 2018

Methods and compositions for treatment of acute lung injury

Inventor: Michael D. Gunn (Chapel Hill, NC)
Assignee: Duke University
A61K31/198A61K9/0019A61K9/0053
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,901,560
App. No.
15/379,063
Granted
Feb 27, 2018
Kind
B2
Abstract

A method of treating acute lung injury (ALI) in a patient suspected of having ALI is disclosed. The method includes administering to the patient a therapeutically effective amount of an inducible nitric oxide synthase (iNOS) inhibitor.

Claims (39)

1. A method of treating acute lung injury (ALI) in a patient suspected of having ALI, the method comprising:

administering to the patient a therapeutically effective amount of an inducible nitric oxide synthase (iNOS) inhibitor, wherein the iNOS inhibitor is (S)-2-amino-(1-iminoethylamino)-5-thioheptanoic acid (GW274150).

2. The method of claim 1 , wherein the ALI is induced by inhalation or aspiration of a chemical irritant.

3. The method of claim 2 , wherein the chemical irritant is selected from a group consisting of chlorine gas, smoke, phosgene, and combinations thereof.

4. The method of claim 1 , wherein the administering comprises orally administering, intravenous administering, intramuscular administering or aerosol administering.

5. The method of claim 4 , wherein the administering comprises orally administering the iNOS inhibitor in an amount between 0.1 mg/Kg to 6.0 mg/Kg.

6. The method of claim 4 , wherein the administering comprises intravenous administering the iNOS inhibitor in an amount between 0.1 mg/Kg to 6.0 mg/Kg.

7. The method of claim 4 , wherein the administering comprises intramuscular administering the iNOS inhibitor in an amount between 0.1 mg/Kg to 6.0 mg/Kg.

8. The method of claim 1 , the method further comprising one or more of the following steps:

monitoring an alveolar-arterial oxygen gradient in the patient before or after the administering;

monitoring a ratio of arterial oxygen partial pressure to fractional inspired oxygen (PaO 2 /FiO 2 ratio) in the patient before or after the administering;

monitoring an oxygenation index in the patient before or after the administering;

monitoring an airway resistance in the patient before or after the administering;

monitoring a peak inspiratory pressure in the patient before or after the administering;

monitoring a lung dynamic compliance in the patient before or after the administering;

monitoring an oxygen saturation drop in the patient before or after the administering;

monitoring a mean airway pressure in the patient before or after the administering; or

monitoring a lung vascular leakage in the patient before or after the administering.

9. A method of treating acute lung injury (ALI) in a patient suspected of having ALI, the method comprising:

a) measuring one or more properties in the patient, the one or more properties selected from the group consisting of:

a ratio of arterial oxygen partial pressure to fractional inspired oxygen (PaO 2 /FiO 2 ratio) in the patient;

an oxygenation index in the patient;

an airway resistance in the patient;

a peak inspiratory pressure in the patient;

a lung dynamic compliance in the patient;

an oxygen saturation drop in the patient;

a mean airway pressure in the patient before;

a lung vascular leakage in the patient; and

combinations thereof;

b) subsequent to step a), administering to the patient a therapeutically effective amount of an inducible nitric oxide synthase (iNOS) inhibitor, wherein the iNOS inhibitor is (S)-2-amino-(1-iminoethylamino)-5-thioheptanoic acid (GW274150); and

c) subsequent to step b), monitoring the one or more properties in the patient.

10. The method of claim 9 , wherein the ALI is induced by inhalation or aspiration of a chemical irritant.

11. The method of claim 10 , wherein the chemical irritant is selected from a group consisting of chlorine gas, smoke, phosgene, and combinations thereof.

12. The method of claim 9 , wherein the administering comprises orally administering, intravenous administering, intramuscular administering or aerosol administering.

13. The method of claim 12 , wherein the administering comprises orally administering the iNOS inhibitor in an amount between 0.1 mg/Kg to 6.0 mg/Kg.

14. The method of claim 9 , wherein the administering comprises intravenous administering.

15. The method of claim 14 , wherein the administering comprises intravenous administering the iNOS inhibitor in an amount between 0.1 mg/Kg to 6.0 mg/Kg.

16. The method of claim 9 , wherein the administering comprises intramuscular administering.

17. The method of claim 16 , wherein the administering comprises intramuscular administering the iNOS inhibitor in an amount between 0.1 mg/Kg to 6.0 mg/Kg.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 19, 2018
From: DUKE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045983/0723 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2017
From: GUNN, MICHAEL D.
To: DUKE UNIVERSITY
Reel/Frame 041465/0929 →
Continuity (2)
Provisional Application 62267635 · Dec 15, 2015
Related Publication 20170165216A1 · Jun 15, 2017