IP Library Granted Patent US 11,197,848
Granted Patent B2
US 11,197,848 · App. 16/425,028 · Granted Dec 14, 2021

Topical amlodipine salts for the treatment of anorectal diseases

Inventors: László Ritter (Budapest, HU); László Hornok (Nagykovácsi, HU); Péter Mátyus (Budapest, HU); Romána Zelkó (Budapest, HU); Andrea Ujhelyi (Nyiregyhaza, HU); Richárd Balázs Kárpáti (Tatabánya, HU); Tamás Solymosi (Békéscsaba, HU); Hristos Glavinas (Szeged, HU)
A61K31/4422A61K9/0014
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Quick Facts
Patent No.
US 11,197,848
App. No.
16/425,028
Granted
Dec 14, 2021
Kind
B2
Abstract

Provided is a topical pharmaceutical gel composition of an amlodipine salt and methods for its use in the treatment of anorectal disease.

Claims (12)

1. A stable topical pharmaceutical gel composition of amlodipine besylate comprising:

about 0.01-1% w/w of amlodipine besylate, as measured as the free base, wherein said amlodipine besylate is present in a dissolved state in said gel, and wherein the degradation impurities of said amlodipine besylate is less than about 2.5% for a storage period of at least 24 months at a temperature of about 2-8° C.;

about 5-75% w/w of at least one glycol solvent;

about 0.1-10% w/w of hydroxyethyl cellulose;

about 30-50% w/w of glycerin;

about 5-15% w/w of ethanol; and

about 15-35% w/w of water.

2. The stable topical pharmaceutical gel composition according to claim 1 , wherein said at least one glycol solvent is chosen from propylene glycol, polyethylene glycol, ethylene glycol, butylene glycol, hexylene glycol, and mixtures thereof.

3. The stable topical pharmaceutical gel composition according to claim 2 , wherein said glycol solvent is propylene glycol.

4. The stable topical pharmaceutical gel composition according to claim 1 , wherein said amlodipine besylate is present at a concentration of 0.01-1% w/w as measured as the free base, wherein said at least one glycol solvent is propylene glycol and is present at a concentration of 5-75% w/w, wherein said hydroxyethyl cellulose is present at a concentration of 0.1-10% w/w, wherein said glycerin is present at a concentration of 30-50% w/w, wherein said ethanol is present at a concentration of 5-15% w/w, wherein said water is present at a concentration of 15-35% w/w, wherein said stable topical pharmaceutical gel composition further comprises methyl parahydroxybenzoate, and wherein said methyl parahydroxybenzoate is present at a concentration of 0.01-5% w/w.

5. The stable topical pharmaceutical gel composition according to claim 1 , wherein said amlodipine besylate is present at a concentration of about 0.1-1% w/w, as measured as the free base.

6. The stable topical pharmaceutical gel composition according to claim 4 , wherein the degradation impurities of said amlodipine besylate is less than 2.5% for a storage period of at least 24 months at a temperature of about 2-8° C.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 8, 2025
From: TAVANTA THERAPEUTICS HUNGARY INCORPORATED
To: TAVANTA THERAPEUTICS, INC.
Reel/Frame 071355/0580 →
CHANGE OF NAME Recorded Nov 18, 2020
From: NANGENEX NANOTECHNOLOGY INCORPORATED
To: TAVANTA THERAPEUTICS HUNGARY INCORPORATED
Reel/Frame 054412/0305 →
MERGER Recorded Mar 3, 2020
From: DRUGGABILITY TECHNOLOGIES IP HOLDCO LIMITED
To: NANGENEX NANOTECHNOLOGY INCORPORATED
Reel/Frame 052000/0924 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2019
From: RITTER, LÁSZLÓ; HORNOK, LÁSZLÓ; MÁTYUS, PÉTER; ZELKÓ, ROMÁNA; UJHELYI, ANDREA; KÁRPÁTI, RICHÁRD BALÁZS; SOLYMOSI, TAMÁS; GLAVINAS, HRISTOS
To: DRUGGABILITY TECHNOLOGIES IP HOLDCO LTD.
Reel/Frame 049417/0411 →
Continuity (3)
Provisional Application 62822400 · Mar 22, 2019
Provisional Application 62679137 · Jun 1, 2018
Related Publication 20190365732A1 · Dec 5, 2019