IP Library Granted Patent US 10,137,128
Granted Patent B2
US 10,137,128 · App. 14/788,211 · Granted Nov 27, 2018

Methods of improving myocardial performance in fontan patients using udenafil compositions

Inventors: James L. Yeager (Lake Forest, IL); David J. Goldberg (Philadelphia, PA); Stephen M. Paridon (Strafford, PA)
Assignees: Mezzion Pharma Co., Ltd.; The Children's Hospital of Philadelphia
A61K31/522A61K31/00
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 10,137,128
App. No.
14/788,211
Granted
Nov 27, 2018
Kind
B2
Abstract

The present invention relates generally to the field of using udenafil or a pharmaceutically acceptable salt thereof in patients who have undergone the Fontan operation.

Claims (17)

1. A method of treating an adolescent with single ventricle heart disease for improving the adolescent's exercise capacity or for increasing the likelihood of improving the adolescent's exercise capacity, whose exercise capacity is adversely affected due to a decline in the adolescent's heart function after Fontan palliation, wherein the adolescent is in need of treatment to improve the adolescent's exercise capacity, or to increase the likelihood of improving the adolescent's exercise capacity as determined by maximum oxygen uptake at maximum exercise output (VO 2 measurement), said method comprising:

orally administering to the adolescent in accordance with a treatment regimen an oral dosage form comprising an effective dose of udenafil, or a pharmaceutically acceptable salt thereof, to improve the adolescent's VO 2 measurement or to increase the likelihood of improving the adolescent's VO 2 measurement for improving the adolescent's exercise capacity or for increasing the likelihood of improving the adolescent's exercise capacity,

wherein the adolescent is a human,

wherein the adolescent has undergone Fontan surgery,

wherein the human adolescent is between about 12 years old and under about 18 years old,

wherein the effective dose of udenafil, or a pharmaceutically acceptable salt thereof, is about 87.5 mg, and

wherein the treatment regimen comprises orally administering the oral dosage form to the human adolescent twice daily.

2. The method of claim 1 , wherein the oral dosage form is a tablet.

3. The method of claim 1 , wherein the oral dosage form is a solid or semi-solid oral dosage form selected from a group consisting of a tablet, a capsule, a gel, a pill, a powder and a suspension.

4. A method of treating an adolescent with single ventricle heart disease for improving the adolescent's exercise capacity or for increasing the likelihood of improving the adolescent's exercise capacity, whose exercise capacity is adversely affected due to a decline in the adolescent's heart function after Fontan palliation, wherein the adolescent is in need of treatment to improve the adolescent's exercise capacity, or to increase the likelihood of improving the adolescent's exercise capacity as determined by maximum oxygen uptake at maximum exercise output (VO 2 measurement), said method comprising:

orally administering to the adolescent in accordance with a treatment regimen an oral dosage form comprising an effective dose of udenafil, or a pharmaceutically acceptable salt thereof, to improve the adolescent's VO 2 measurement or to increase the likelihood of improving the adolescent's VO 2 measurement for improving the adolescent's exercise capacity or for increasing the likelihood of improving the adolescent's exercise capacity,

wherein the adolescent is a human,

wherein the adolescent has undergone Fontan surgery,

wherein the human adolescent is between about 12 years old and under about 18 years old, and

wherein the total daily dose of udenafil, or a pharmaceutically acceptable salt thereof, is from about 125 mg to about 175 mg.

5. The method of claim 4 , wherein the oral dosage form is a tablet.

6. The method of claim 4 , wherein the oral dosage form is a solid or semi-solid oral dosage form selected from a group consisting of a tablet, a capsule, a gel, a pill, a powder and a suspension.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2024
From: YEAGER, JAMES L.
To: MEZZION PHARMA CO., LTD.
Reel/Frame 068608/0686 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2017
From: YEAGER, JAMES L.
To: MEZZION PHARMA CO., LTD.
Reel/Frame 042708/0978 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 22, 2017
From: GOLDBERG, DAVID; PARIDON, STEPHEN
To: THE CHILDREN'S HOSPITAL OF PHILADELPHIA
Reel/Frame 042455/0603 →
Continuity (3)
Provisional Application 62036506 · Aug 12, 2014
Provisional Application 62186132 · Jun 29, 2015
Related Publication 20160045510A1 · Feb 18, 2016
Cited By (1)
US 12,576,081