IPR decision (Aug 07, 2018):
AIA Review
|
Filing Date
|
Institution Date
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Petitioner
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Patent No.
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Final Written
Decision
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IPR2017-01446
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05/16/2017
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11/28/2017
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Taro Pharma
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7,049,328
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Terminated-Settled
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Litigation status: In May 2016, Apopharma sued Taro in Eastern District Court of Texas for
infringement of US’328 patent. Bench trial is scheduled on 10/22/18.
US 7,049,328 (Apotex Inc; Exp: 06/28/2021) – listed in
OB
1. A method of treating iron induced cardiac disease in a
blood transfusion dependent patient experiencing an iron overload condition of the
heart, said method comprising administering to the patient a therapeutically
effective amount of deferiprone or a physiologically acceptable salt thereof
sufficient to stabilize/reduce iron accumulation in the heart resulting from
being transfusion dependent.
2. A method of treating iron loading in the heart of a blood
transfusion dependent patient experiencing an iron overload condition of the
heart, said method comprising administering to the transfusion dependent
patient a therapeutically effective amount of deferiprone or a physiologically
acceptable salt thereof sufficient to reduce further iron overload in the heart
normally associated with iron induced cardiac disease.
3. A method of treating iron loading in the heart of a blood
transfusion dependent patient risking iron overload of the heart, comprising
the administration of a therapeutically effective amount of deferiprone or a
physiologically acceptable salt thereof to the patient.
4. A method of stabilizing iron induced heart disease in blood
transfusion dependent patients having iron overload, comprising the
administration of a therapeutically effective amount of deferiprone or a
physiologically acceptable salt thereof sufficient to treat the iron burden in
the heart normally associated with iron induced cardiac disease.
5. A method of reducing the iron burden in the heart
associated with iron induced heart disease in blood transfusion dependent
patients having iron overload, comprising the administration of a
therapeutically effective amount of deferiprone or a physiologically acceptable
salt thereof sufficient to reduce the iron burden of the heart normally
associated with iron induced cardiac disease.
6. A method of treating iron induced heart disease in a
blood transfusion dependent patient having an iron overload condition of the
heart comprising administering to the patient a therapeutically effective
amount of deferiprone, or a physiologically acceptable salt thereof in order to
reduce the iron stores in the heart in preference to general iron stores in the
body, such as found in the liver.
7. A method of treating iron loading in the heart of blood
transfusion dependent patient having an iron overload condition of the heart
comprising administering to the patient a therapeutically effective amount of
deferiprone or a physiologically acceptable salt thereof to chelate the iron
stores in the heart in preference to general iron stores in the body, such as
found in the liver.
8. A method of treating iron loading in the heart of blood
transfusion dependent patient having an iron overload condition of the heart
comprising administering to the patient a therapeutically effective amount of
deferiprone or a physiologically acceptable salt thereof to reduce the iron
stores in the heart in preference to general iron stores organs/tissue in the
body, such as found in the liver.
9. A method of treatment of iron induced heart disease in a
blood transfusion dependent patient having an iron overload condition of the
heart comprising administering to the patient a therapeutically effective
amount of deferiprone or a physiologically acceptable salt thereof for the
direct reduction/removal of intracellular iron stores in the heart.
10. A method to reduce the occurrence of iron-induced
cardiac disease in a blood transfusion dependent patient with an iron overload
condition, comprising administering to said patient a therapeutically effective
amount of deferiprone or a physiologically acceptable salt thereof, wherein
deferiprone's efficacy is cardio preferential when compared with its ability to
lower total iron stores in the body.
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