US2014154205A1PendingUtilityA1
Erythropoietin and fibronectin compositions for therapeutic and cosmetic applications
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-modifiedWhat 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.Join the waitlist — get patent alerts
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