IP Library Granted Patent US 11,278,544
Granted Patent B2
US 11,278,544 · App. 16/363,206 · Granted Mar 22, 2022

Compositions for affecting weight loss

Inventors: Eckard Weber (San Diego, CA); Michael Alexander Cowley (Portland, OR)
Assignee: Nalpropion Pharmaceuticals LLC
A61K31/485A61K31/135A61K31/137A61K31/138A61K45/06A61K31/35A61P3/04Y10S514/909Y10S514/964
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 11,278,544
App. No.
16/363,206
Granted
Mar 22, 2022
Kind
B2
Abstract

Disclosed are compositions for affecting weight loss comprising a first compound and a second compound, where the first compound is an opioid antagonist and the second compound causes increased agonism of a melanocortin 3 receptor (MC3-R) or a melanocortin 4 receptor (MC4-R) compared to normal physiological conditions. Also disclosed are methods of affecting weight loss, increasing energy expenditure, increasing satiety in an individual, or suppressing the appetite of an individual, comprising identifying an individual in need thereof and treating that individual to antagonize opioid receptor activity and to enhance α-MSH activity.

Claims (7)

1. A method of treating overweight or obesity, the method comprising administering to a patient in need thereof a therapeutically effective amount comprising 30 mg to 500 mg of bupropion, or a pharmaceutically acceptable salt thereof, and a therapeutically effective amount comprising 5 mg to 50 mg of naltrexone, or a pharmaceutically acceptable salt thereof, wherein the bupropion or pharmaceutically acceptable salt thereof is in a sustained-release formulation.

2. The method of claim 1 , wherein the naltrexone or pharmaceutically acceptable salt thereof is in a sustained-release formulation.

3. The method of claim 1 , wherein the therapeutically effective amount comprises 30 mg to 300 mg of bupropion or a pharmaceutically acceptable salt thereof.

4. The method of claim 1 , wherein the naltrexone or pharmaceutically acceptable salt thereof and bupropion or pharmaceutically acceptable salt thereof are administered simultaneously.

5. The method of claim 1 , wherein the naltrexone or pharmaceutically acceptable salt thereof and bupropion or pharmaceutically acceptable salt thereof are provided in a single oral dosage form.

6. The method of claim 1 , wherein the naltrexone or pharmaceutically acceptable salt thereof is administered prior to the bupropion or pharmaceutically acceptable salt thereof.

7. The method of claim 1 , wherein the naltrexone or pharmaceutically acceptable salt thereof is administered subsequent to the bupropion or pharmaceutically acceptable salt thereof.

Assignments (4)
SECURITY INTEREST Recorded Dec 19, 2019
From: CURRAX PHARMACEUTICALS LLC; NALPROPION PHARMACEUTICALS LLC
To: WILMINGTON SAVINGS FUND SOCIETY, FSB
Reel/Frame 051377/0958 →
CHANGE OF NAME Recorded Oct 17, 2019
From: NALPROPION PHARMACEUTICALS, INC.
To: NALPROPION PHARMACEUTICALS LLC
Reel/Frame 050750/0497 →
RELEASE OF SECURITY INTEREST Recorded Sep 27, 2019
From: WILMINGTON SAVINGS FUND SOCIETY, FSB
To: NALPROPION PHARMACEUTICALS, INC.
Reel/Frame 050520/0149 →
SECURITY INTEREST Recorded May 6, 2019
From: NALPROPION PHARMACEUTICALS, INC.
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS COLLATERAL AGENT
Reel/Frame 049092/0156 →