US2014154205A1PendingUtilityA1

Erythropoietin and fibronectin compositions for therapeutic and cosmetic applications

Assignee: REMEDOR BIOMED LTDPriority: Aug 16, 2007Filed: Feb 10, 2014Published: Jun 5, 2014
Est. expiryAug 16, 2027(~1 yrs left)· nominal 20-yr term from priority
Inventors:Saher Hamed
A61P 43/00A61P 7/04A61P 9/10A61P 39/04A61P 3/02A61P 31/00A61K 31/70A61K 38/19A61K 38/39A61K 9/06A61K 38/1816A61K 38/22A61K 31/198A61K 9/0014A61K 38/43A61K 47/32A61P 17/02A61K 31/21A61K 38/36
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Claims

Abstract

A method of promoting wound healing or connective tissue reconstruction and a method of treating ischemia in a subject in need thereof are disclosed. The methods comprising topically administering to the subject about 10-30 mg per cm 2 wound tissue of Erythropoietin and about 100-300 mg per cm 2 wound tissue of Fibronectin, thereby promoting wound healing or connective tissue reconstruction or treating ischemia in the subject. Unit dosage forms, pharmaceutical compositions, cosmetic compositions and formulations comprising Erythropoietin and/or Fibronectin are also disclosed.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of promoting wound healing or connective tissue reconstruction in a subject in need thereof, the method comprising topically administering to the subject about 10-30 μg per cm 2  tissue of Erythropoietin and about 100-300 μg per cm 2  tissue of Fibronectin, thereby promoting wound healing or connective tissue reconstruction in the subject. 
     
     
         2 . A method of treating ischemia in a subject in need thereof, the method comprising topically administering to the subject about 10-30 μg per cm 2  tissue of Erythropoietin and about 100-300 μg per cm 2  tissue of Fibronectin, thereby treating ischemia in the subject. 
     
     
         3 . The method of  claim 1 , wherein the connective tissue comprises collagen. 
     
     
         4 . The method of  claim 1 , wherein a dose of said Erythropoietin is about 20 μg per cm 2  tissue. 
     
     
         5 . The method of  claim 1 , wherein a dose of said Fibronectin is about 200 μg per cm 2  tissue. 
     
     
         6 . The method of  claim 1 , further comprising administering a factor selected from the group consisting of an extracellular matrix component, a growth factor, a hormone, an angiogenic factor, a coagulation factor, a cytokine, a chemokine, an enzyme, a neurotransmitter, a vitamin, a carbohydrate, an ion, an iron chelator, a fatty acid, an antibiotic, and an amino acid. 
     
     
         7 . The method of  claim 1 , wherein said administering of said Erythropoietin and said Fibronectin is effected concomitantly. 
     
     
         8 . The method of  claim 1 , wherein said Erythropoietin and said Fibronectin are in a co-formulation. 
     
     
         9 . The method of  claim 1 , wherein said Erythropoietin and said Fibronectin are in separate formulations. 
     
     
         10 . The method of  claim 2 , wherein a dose of said Erythropoietin is about 20 μg per cm 2  tissue. 
     
     
         11 . The method of  claim 2 , wherein a dose of said Fibronectin is about 200 μg per cm 2  tissue. 
     
     
         12 . The method of  claim 2 , further comprising administering a factor selected from the group consisting of an extracellular matrix component, a growth factor, a hormone, an angiogenic factor, a coagulation factor, a cytokine, a chemokine, an enzyme, a neurotransmitter, a vitamin, a carbohydrate, an ion, an iron chelator, a fatty acid, an antibiotic, and an amino acid. 
     
     
         13 . The method of  claim 2 , wherein said administering of said Erythropoietin and said Fibronectin is effected concomitantly. 
     
     
         14 . The method of  claim 2 , wherein said Erythropoietin and said Fibronectin are in a co-formulation. 
     
     
         15 . The method of  claim 2 , wherein said Erythropoietin and said Fibronectin are in separate formulations. 
     
     
         16 . The method of  claim 1 , wherein the active ingredients administered to said subject consist of Erythropoietin and Fibronectin. 
     
     
         17 . The method of  claim 1 , wherein said administering is effected at least once a day. 
     
     
         18 . A pharmaceutical composition comprising as an active ingredient about 10-30 μg per ml Erythropoietin and about 100-300 μg per ml Fibronectin and a pharmaceutically acceptable carrier or diluent for topical administration.

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