US2011060041A1PendingUtilityA1

Method of reversing, preventing, delaying or stabilizing soft tissue calcification

Assignee: HSU CHEN HSINGPriority: Jan 30, 2006Filed: Jun 22, 2010Published: Mar 10, 2011
Est. expiryJan 30, 2026(expired)· nominal 20-yr term from priority
A61P 43/00A61P 39/00A61P 7/08A61P 5/18A61P 9/00A61P 3/00A61P 27/02A61P 3/14A61P 3/12A61P 19/08A61P 19/02A61P 17/00A61P 13/12A61P 19/00A61P 11/00A61K 31/295A61K 9/143A61K 31/555A61K 33/26C07C 51/412
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Claims

Abstract

The present invention provides methods of treating soft tissue calcification in a subject, comprising a step of administering to said subject an effective amount of ferric organic compound, such as ferric citrate. The claimed methods may prevent, reverse, delay or stabilize soft tissue calcification in a subject having chronic kidney disease. Affected soft tissue calcification includes soft tissue calcification in the joint, skin, eye, in cardiovascular system such as heart valve, myocardium, coronary arteries and arteriole, or in internal organs such as kidney and lung.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating soft tissue calcification in a subject, comprising administering to said subject an effective amount of a ferric organic compound. 
     
     
         2 . The method of  claim 1 , wherein the subject is a human or an animal. 
     
     
         3 . The method of  claim 1 , wherein the subject is having chronic kidney disease or end stage renal disease. 
     
     
         4 . The method of  claim 1 , wherein the subject is undergoing renal dialysis or renal transplantation. 
     
     
         5 . The method of  claim 1 , wherein soft tissue calcification in the subject is reversed, delayed, stabilized, or prevented. 
     
     
         6 . The method of  claim 1 , wherein the soft tissue is tissue in joint, skin, eye, heart valve, myocardium, coronary arteries or arterioles, kidney, or lung. 
     
     
         7 . The method of  claim 1 , wherein the ferric organic compound is in a form suitable for oral administration. 
     
     
         8 . The method of  claim 7 , wherein the form suitable for oral administration is a tablet, a powder, a suspension, an emulsion, a capsule, a lozenge, a granule, a troche, a pill, a liquid, a spirit, or a syrup. 
     
     
         9 . The method of  claim 1 , wherein the ferric organic compound is ferric citrate.

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