IP Library › Granted Patent US 11,484,531
Granted Patent B2
US 11,484,531 · App. 16/555,216 · Granted Nov 1, 2022

Methods for treating chronic obstructive pulmonary disease

Inventors: Christopher Noel Barnes (South San Francisco, CA); Glenn D. Crater (South San Francisco, CA); Edmund J. Moran (South San Francisco, CA); Srikanth Pendyala (South San Francisco, CA)
Assignee: THERAVANCE BIOPHARMA R&D IP, LLC
A61K31/444A61K9/0078A61K31/135A61P11/06A61K45/06
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Quick Facts
Patent No.
US 11,484,531
App. No.
16/555,216
Granted
Nov 1, 2022
Kind
B2
Abstract

Methods for treating chronic obstructive pulmonary disease (COPD) in a patient are disclosed. In the methods, a patient having COPD is selected for treatment based on the patient's peak inspiratory flow rate (PIFR) and percent predicted force expiratory volume in one second (FEV 1 ); and a bronchodilator is administered to the selected patient using a nebulizer. Administration of a bronchodilator to patients having low PIFR and a percent predicted FEV 1 less than 50 percent using a nebulizer as the inhalation delivery device provides significantly greater improvements in trough FEV 1 and trough forced vital capacity (FVC) compared to administration of a bronchodilator to such patients using a dry powder inhaler.

Claims (12)

1. A method for treating chronic obstructive pulmonary disease in a patient, the method comprising:

(a) selecting a patient having chronic obstructive pulmonary disease for treatment based on the patient having a peak inspiratory flow rate less than about 60 L/min and a percent predicted force expiratory volume in one second less than about 50 percent; and

(b) administering a pharmaceutical composition comprising about 175 μg of revefenacin, or a pharmaceutically acceptable salt thereof, in 3 mL of an aqueous solution to the selected patient once daily using a nebulizer.

2. The method of claim 1 , wherein the patient has a peak inspiratory flow rate less than about 50 L/min.

3. The method of claim 1 , wherein the patient has a percent predicted force expiratory volume in one second less than about 40 percent.

4. The method of claim 1 , wherein the patient has a peak inspiratory flow rate in the range of about 20 L/min to less than about 60 L/min and a percent predicted force expiratory volume in one second in the range of from about 20 percent to less than about 50 percent.

5. The method of any one of claims 1 to 4 , wherein the pharmaceutical composition has a pH in the range of about 4.5 to about 5.5.

6. The method of any one of claims 1 to 4 , wherein the pharmaceutical composition has a pH of about 4.8 to about 5.2.

7. The method of any one of claims 1 to 4 , wherein the pharmaceutical composition is isotonic.

8. The method of any one of claims 1 to 4 , wherein the pharmaceutical composition further comprises sodium chloride, citric acid and sodium citrate.

9. The method of any one of claims 1 to 4 , wherein the pharmaceutical composition is sterile, isotonic and has a pH of about 4.8 to about 5.2.

10. The method of any one of claims 1 to 4 , wherein the pharmaceutical composition is administered using a jet nebulizer.

Assignments (2)
SECURITY INTEREST Recorded Sep 24, 2026
From: THERAVANCE BIOPHARMA R&D IP, LLC
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION
Reel/Frame 076134/0790 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2019
From: BARNES, CHRISTOPHER NOEL; CRATER, GLENN D.; MORAN, EDMUND J.; PENDYALA, SRIKANTH
To: THERAVANCE BIOPHARMA R&D IP, LLC
Reel/Frame 051235/0684 →
Continuity (2)
Provisional Application 62724805 · Aug 30, 2018
Related Publication 20200069667A1 · Mar 5, 2020
Cited By (1)
US 12,285,417