IP Library Granted Patent US 11,759,441
Granted Patent B2
US 11,759,441 · App. 17/375,807 · Granted Sep 19, 2023

Biguanide compositions and methods of treating metabolic disorders

Inventors: Alain D. Baron (San Diego, CA); Mark S. Fineman (San Diego, CA); Nigel R. A. Beeley (Solana Beach, CA)
Assignee: Anji Pharmaceuticals Inc.
A61K31/155A61K9/2086A61K9/2806A61K9/4808A61K31/137A61K31/341A61K31/35A61K31/36A61K31/381A61K31/40A61K31/4196A61K31/4453A61K31/454A61K31/485A61K31/53A61K31/55A61K45/06A61P3/08A61P3/10
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 11,759,441
App. No.
17/375,807
Granted
Sep 19, 2023
Kind
B2
Abstract

Provided herein are methods for treating certain conditions, including diabetes, obesity, and other metabolic diseases, disorders or conditions by administrating a composition comprising a biguanide or related heterocyclic compound, e.g., metformin. Also provided herein are biguanide or related heterocyclic compound compositions, and methods for the preparation thereof for use in the methods of the present invention. Also provided herein are compositions comprising metformin and salts thereof and methods of use.

Claims (13)

1. A method for treating diabetes in a patient in need thereof comprising administering to said patient a pharmaceutical dosage form comprising metformin or a salt thereof, wherein said pharmaceutical dosage form is adapted to have an onset of release of said metformin or a salt thereof downstream of the duodenum and to provide at least 20% less relative bioavailability of metformin as measured by plasma area under curve (AUC) resulting from administration of said pharmaceutical dosage form compared to an immediate release composition having the same amount of said metformin or a salt thereof, and wherein the daily dose of said metformin or a salt thereof is between 1500 mg and 2000 mg of metformin.

2. The method of claim 1 , wherein the circulating plasma concentration of metformin resulting from administration of said pharmaceutical dosage form is below 1.0 μg/mL.

3. The method of claim 1 , wherein the circulating plasma concentration of metformin resulting from administration of said pharmaceutical dosage form is below 0.5 μg/mL.

4. The method of claim 1 , wherein the circulating plasma concentration of metformin resulting from administration of said pharmaceutical dosage form is below 0.25 μg/mL.

5. The method of claim 1 , wherein said pharmaceutical dosage form is adapted to provide at least 30% less relative bioavailability of metformin compared to an immediate release composition having the same amount of said metformin or a salt thereof.

6. The method of claim 1 , wherein said pharmaceutical dosage form is adapted to provide at least 40% less relative bioavailability of metformin compared to an immediate release composition having the same amount of said metformin or a salt thereof.

7. The method of claim 1 , wherein said pharmaceutical dosage form is adapted to provide at least 50% less relative bioavailability of metformin compared to an immediate release composition having the same amount of said metformin or a salt thereof.

8. The method of claim 1 , wherein said pharmaceutical dosage form is adapted to have an onset of release of said metformin or a salt thereof downstream of the jejunum.

9. The method of claim 1 , wherein said pharmaceutical dosage form is adapted to have an onset of release of said metformin or a salt thereof downstream of the ileum.

10. The method of claim 1 , wherein said metformin or a salt thereof is metformin hydrochloride.

11. The method of claim 1 , wherein said pharmaceutical dosage form has an onset of release of said metformin or a salt thereof at about pH 6.0.

12. The method of claim 1 , wherein said pharmaceutical dosage form has an onset of release of said metformin or a salt thereof at about pH 6.5.

13. The method of claim 1 , wherein said pharmaceutical dosage form has an onset of release of said metformin or a salt thereof at about pH 7.0.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 2, 2023
From: ANJI PHARMA (US) LLC
To: ANJI PHARMACEUTICALS INC.
Reel/Frame 062859/0218 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2021
From: BARON, ALAIN D.; FINEMAN, MARK S.; BEELEY, NIGEL R.A.
To: ELCELYX THERAPEUTICS, INC.
Reel/Frame 057660/0301 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2021
From: ELCELYX THERAPEUTICS, INC.
To: ANJI PHARMA (US) LLC
Reel/Frame 057679/0075 →
Continuity (7)
Continuation 16223002 · Dec 17, 2018
Continuation 15339346 · Oct 31, 2016
Continuation 14370449
Continuation In Part PCTUS2012020548 · Jan 6, 2012
Continuation In Part 13345135 · Jan 6, 2012
Provisional Application 61649171 · May 18, 2012
Related Publication 20220151957A1 · May 19, 2022