US2006122273A1PendingUtilityA1
Use for deferiprone
Est. expiryJun 30, 2020(expired)· nominal 20-yr term from priority
A61P 9/00A61P 43/00A61K 31/4412A61K 31/44A61P 7/06
44
PatentIndex Score
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Claims
Abstract
A method of treating iron induced cardiac disease in a patient with iron overload, such as in thalassemia or the like comprising administering to the patient a therapeutically effective amount of deferiprone or a physiologically acceptable salt thereof sufficient to treat induced cardiac disease normally associated with iron overload.
Claims
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8 . A pharmaceutical composition comprising an effective therapeutic amount of deferiprone or a physiologically acceptable salt thereof for the prevention of heart disease in transfusion dependent patients experiencing iron overload and sufficient to treat iron induced cardiac disease normally associated with iron overload.
9 . A pharmaceutical composition comprising an effective therapeutic amount of deferiprone or a physiologically acceptable salt thereof for the stabilization of heart disease in transfusion dependent patients experiencing iron overload and sufficient to treat iron induced cardiac disease normally associated with iron overload.
10 . A pharmaceutical composition comprising an effective therapeutic amount of deferiprone or a physiologically acceptable salt thereof for the reduction of heart disease in transfusion dependent patients experiencing iron overload and sufficient to treat iron induced cardiac disease normally associated with iron overload.
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18 . A pharmaceutical composition comprising a therapeutically effective amount of deferiprone or physiologically acceptable salt thereof for the prevention, treatment, or reversal of heart disease in transfusion dependent patients experiencing an iron overload condition of the heart and to preferentially reduce the iron stores in the heart in comparison to the iron stores in other organs/tissue in the body.
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54 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 further comprising an oral dosage form of deferiprone or a physiologically acceptable salt thereof with other excipients.
55 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 further comprising daily administration of an amount of deferiprone or a physiologically acceptable salt thereof substantially in the range of up to 150 mg/kg of body weight.
56 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 further comprising administration of a daily dosage amount of deferiprone or a physiologically acceptable salt thereof substantially in the range of up to 125 mg/kg of body weight.
57 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 further comprising administration of a daily dosage amount of deferiprone or a physiologically acceptable salt thereof substantially in the range of 25 mg/kg to 75 mg/kg of body weight.
58 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 is administered in a manner selected from the group of intravenously, transdermally, rectally, orally, bucally, or aurally.
59 . The pharmaceutical composition of claim 58 wherein deferiprone is administered orally.
60 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 wherein the composition is in a sustained release formulation.
61 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 wherein deferiprone has a cardio preferred/selective function when compared to desferrioxamine or other alternative chelating agents utilized in patients suffering iron overload.
62 . The pharmaceutical composition of claims 8 , 9 , 10 and 18 wherein desferrioxamine is administered in addition to deferiprone.Join the waitlist — get patent alerts
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