Low Dosage Forms Of Risedronate Or Its Salts

a risedronate and low dosage technology, applied in the field of oral dosage forms of risedronate, can solve the problems of inability to apply edta as an agent in human pharmacotherapy, reduced cancellous bone strength, topical irritation, etc., and achieves the effects of reducing the absorption of risedronate, and increasing patient complian

Inactive Publication Date: 2008-11-20
WARNER CHILCOTT CO LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0019]The dosage forms of the present invention provide an immediate release of risedronate and the chelating agent to the small intestine of the mammal subject and pharmaceutically effective absorption of risedronate active ingredient when administered with or without food or beverages.
[0020]The present invention substantially alleviates the interaction between risedronate and food, which interaction results in decreased absorption of risedronate. The resulting novel oral dosage form may thus be taken with or wi

Problems solved by technology

Essential quantities of cancellous bone are lost, and marrow and bone spaces become larger, resulting in reduced cancellous bone strength.
It is hypothesized that this irritation results from the bisphosphonate tablet adhering to epithelial and mucosal tissues, resulting in the topical irritation thereof.
While the use of absorption enhancers, such as ethylenediaminetetraacetic acid (EDTA), that increase intestinal permeability at high doses, has been proposed as a means of increasing absorption of oral bisphosphonates, the applicability of EDTA as an agent in human pharmacoth

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example i

Enteric-Coated Tablets Containing Risedronate and EDTA

[0093]Enteric-coated tablets containing risedronate and EDTA are made by preparing a coating composition and compressed tablets containing risedronate and EDTA, and then applying said coating composition to said tablets.

[0094]An enteric coating composition is prepared in the form of a lacquer containing the following excipients, per tablet:

A. Enteric Coating SuspensionIngredients:Eudragit L 30 D-55 ® (wet basis)73.65mg(manufactured by Röhm Pharma GmbH and Co. KG,Darmstadt, Germany)Triethylcitrate2.21mgTalc16.57mgYellow Iron Oxide0.03mgSimethicone0.07mgPolysorbate 800.22mgPurified Water113.2mg

[0095]The enteric coating is prepared using the following method:

[0096]A pigment suspension is prepared by adding polysorbate 80, ground ferric oxide, and talc to approximately three-quarters of the purified water while mixing. The suspension is mixed for at least 60 minutes. The simethicone and the remaining water are added to the pigment su...

example ii

Enteric-Coated Tablets Containing Risedronate and EDTA

[0100]Enteric-coated tablets containing risedronate and EDTA are made by preparing a coating composition and compressed tablets containing risedronate and EDTA, and then applying said coating composition to said tablets.

[0101]An enteric coating composition is prepared in the form of a lacquer containing the following excipients, per tablet:

A. Enteric Coating SuspensionIngredients:Eudragit L 30 D-55 ® (wet basis)77.34mg(manufactured by Röhm Pharma GmbH and Co. KG,Darmstadt, Germany)Triethylcitrate2.32mgTalc17.4mgYellow Iron Oxide0.03mgSimethicone0.07mgPolysorbate 800.23mgPurified Water118.88mg

[0102]The enteric coating is prepared using the following method:

[0103]A pigment suspension is prepared by adding polysorbate 80, ground ferric oxide, and talc to approximately three-quarters of the purified water while mixing. The suspension is mixed for at least 60 minutes. The simethicone and the remaining water are added to the pigment su...

example iii

Enteric-Coated Tablets Containing Risedronate and EDTA

[0107]Enteric-coated tablets containing risedronate and EDTA are made by preparing a coating composition and compressed tablets containing risedronate and EDTA, and then applying said coating composition to said tablets.

[0108]An enteric coating composition is prepared in the form of a lacquer containing the following excipients, per tablet:

A. Enteric Coating SuspensionIngredients:Eudragit L 30 D-55 ® (wet basis)77.34mg(manufactured by Röhm Pharma GmbH and Co. KG,Darmstadt, Germany)Triethylcitrate2.32mgTalc17.4mgYellow Iron Oxide0.03mgSimethicone0.07mgPolysorbate 800.23mgPurified Water118.88mg

[0109]The enteric coating is prepared using the following method:

[0110]A pigment suspension is prepared by adding polysorbate 80, ground ferric oxide, and talc to approximately three-quarters of the purified water while mixing. The suspension is mixed for at least 60 minutes. The simethicone and the remaining water are added to the pigment su...

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Abstract

Oral dosage forms comprising risedronate or a salt thereof, a chelating agent, and means for effecting delayed release of the risedronate (or salt) immediate release of the oral dosage form to the small intestine of the mammal subject and pharmaceutically effective absorption of the bisphosphonate with or without food or beverages. The present invention substantially alleviates the interaction between the risedronate (or salt) and food or beverages, which interaction results in the active ingredient not being available for absorption. The resulting oral dosage form may thus be taken with or without food. Further, disclosed is delivery of risedronate and the chelating agent to the small intestine, substantially alleviating the upper GI irritation associated with bisphosphonate therapies. These benefits simplify previously complex treatment regimens and can lead to increased patient compliance with bisphosphonate therapies.

Description

CROSS REFERENCE TO RELATED APPLICATION[0001]This application is a continuation-in-part of U.S. application Ser. No. 11 / 286,875, filed Nov. 23, 2005, which is a continuation-in-part of U.S. application Ser. No. 11 / 106,816, filed Apr. 15, 2005, which claims the benefit of U.S. Provisional Application Ser. No. 60 / 573,881, May 24, 2004.FIELD OF THE INVENTION[0002]The present invention relates to oral dosage forms of risedronate comprising risedronate, a chelating agent for enabling administration of risedronate with food, and means for effecting delayed release of risedronate and the chelating agent in the small intestine. The oral dosage forms of the invention provide delivery of the pharmaceutical composition to the small intestine of the mammal subject and provide pharmaceutically effective absorption of risedronate when administered with or without food or beverages. The present invention further relates to a method of treating or preventing diseases characterized by abnormal calciu...

Claims

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Application Information

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IPC IPC(8): A61K31/675A61P19/10
CPCA61K9/2013A61K9/2054A61K9/2059A61K9/282A61K9/2846A61K9/2866A61K9/2886A61K9/4891A61K31/198A61K31/663A61K31/675A61K45/06A61K2300/00A61K9/0053A61P19/08A61P19/10
Inventor DANSEREAU, RICHARD JOHNBURGIO, JR., DAVID ERNEST
Owner WARNER CHILCOTT CO LLC
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