Otamixaban formulations with improved stability

Patent metadata

Field	Value
Publication number	US-9993464-B2
Application number	US-201615265191-A
Country	US
Kind code	B2
Filing date	Sep 14, 2016
Priority date	Mar 29, 2011
Publication date	Jun 12, 2018
Grant date	Jun 12, 2018

Abstract

The invention relates to a pharmaceutical composition comprising methyl (2R.3R)-2-{3-[amino(imino)methyl]benzyl}-3-{[4-(1-oxidopyridin-4-yl)benzoyl]amino}butanoate or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable acidic reacting compound or to an aqueous solution or dispersion of the composition as well as a process for the preparation of the same, methods of using such compositions to treat subjects suffering from conditions which can be ameliorated by the administration of an inhibitor of Factor Xa.

First claim

The invention claimed is:

1. A method of minimizing impurities in an aqueous pharmaceutical composition for injection comprising methyl (2R,3R)-2-{3-[amino(imino)methyl]benzyl}-3-{[4-(1-oxidopyridin-4-yl)benzoyl]amino}butanoate, the method comprising the steps of:
a) dissolving methyl (2R,3R)-2-{3-[amino(imino)methyl]benzyl}-3-{[4-(1-oxidopyridin-4-yl)benzoyl]amino}butanoate in water to form a first aqueous solution;
b) dissolving an acidic reacting compound, a salt thereof, or a mixture of the foregoing, in water to form a second aqueous solution;
c) adding the first aqueous solution from step a) to the second aqueous solution from step b) to form a third aqueous solution; and
d) adjusting the pH of the third aqueous solution from step c) to a pH from about 3 to about 5.0 to form the aqueous pharmaceutical composition,

wherein the aqueous pharmaceutical composition comprises from 0.1 mg/mL to 60 mg/mL of methyl (2R,3R)-2-{3-[amino(imino)methyl]benzyl}-3-{[4-(1-oxidopyridin-4-yl)benzoyl]amino}butanoate, and from 1 mMol/L to 1000 mMol/L of the acidic reacting compound, a salt thereof, or a mixture of the foregoing; and
wherein the aqueous pharmaceutical composition contains (i) a maximum impurity level of (2R,3R)-2-(3-Carbamimidoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl)benzoylamino]-butyric acid that does not exceed about 8.0% after storage for 1-6 months at 40° C. and 75% relative humidity, and (ii) a maximum impurity level of (2R,3R)-2-(3-Carbamoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl) benzoylamino]-butyric acid methyl ester that does not exceed about 5.0% after storage for 1-6 months at 40° C. and 75% relative humidity.

2. The method of claim 1 , wherein the acidic reacting compound is selected from the group consisting of citric acid, acetic acid, glycolic acid, lactic acid, pyruvic acid, malonic acid, succinic acid, glutaric acid, fumaric acid, malic acid, tartaric acid, ascorbic acid, maleic acid, hydroxymaleic acid, benzoic acid, hydroxybenzoic acid, phenylacetic acid, cinnamic acid, salicyclic acid, 2-phenoxybenzoic acid, p-toluenesulfonic acid, methanesulfonic acid, 2-hydroxyethanesulfonic acid, hyaluronic acid, and acetyl salicylic acid, or is an amino acid, or is a mineral acid selected from the group consisting of hydrochloric acid and phosphoric acid, or is a salt of said organic acid, amino acid, or mineral acid, or is a mixture of any of the foregoing.

3. The method of claim 2 , wherein the acidic reacting compound is selected from the group consisting of citric acid and sodium citrate, or is a mixture thereof.

4. The method of claim 1 , wherein the aqueous pharmaceutical composition comprises from 1.0 mg/mL to 50 mg/mL of methyl (2R,3R)-2-{3-[amino(imino) methyl]benzyl}-3-{[4-(1-oxidopyridin-4-yl)benzoyl]amino}butanoate, and from 20 mMol/L to 25 mMol/L of the acidic reacting compound, a salt thereof, or a mixture of the foregoing.

5. The method of claim 4 , wherein the aqueous pharmaceutical composition comprises from 1.0 mg/mL to 5 mg/mL methyl of (2R,3R)-2-{3-[amino(imino)methyl]benzyl}-3-{[4-(1-oxidopyridin-4-yl)benzoyl]amino}butanoate, and from 20 mMol/L to 25 mMol/L of the acidic reacting compound, a salt thereof, or a mixture of the foregoing.

6. The method of claim 1 , wherein the pH of the third aqueous solution from step c) is adjusted to a pH from about 3 to about 4.7.

7. The method of claim 6 , wherein the pH of the third aqueous solution from step c) is adjusted to a pH from about 3.7 to about 4.3.

8. The method of claim 6 , wherein the pH of the third aqueous solution from step c) is adjusted to a pH from 4.0 to about 4.2.

9. The method of claim 1 , wherein the maximum impurity level of (2R,3R)-2-(3-Carbamimidoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl)benzoylamino]-butyric acid is from 0.3% to 4.0%.

10. The method of claim 1 , wherein the maximum impurity level of (2R,3R)-2-(3-Carbamimidoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl)benzoylamino]-butyric acid is from 0.4% to 1.8%.

11. The method of claim 1 , wherein the maximum impurity level of (2R,3R)-2-(3-Carbamoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl)benzoylamino]-butyric acid methyl ester is from 0.7% to 4.5%.

12. The method of claim 1 , wherein the maximum impurity level of (2R,3R)-2-(3-Carbamoyl-benzyl)-3-[4-(1-oxy-pyridin-4-yl)benzoylamino]-butyric acid methyl ester is from 0.9% to 3.5%.

13. The method of claim 1 , wherein the aqueous pharmaceutical composition is sterile.

Assignees

• Sanofi Sa

Inventors

• Kamm Walter
• Bussemer Till
• Andert Doris
• Kuehn Bernd
• Todt Ernst-Josef

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P7/02

  Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors · CPC title

• A61P9/10

  for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• A61P19/10

  for osteoporosis · CPC title