US2007196512A1PendingUtilityA1
Combinations of vanadium with antidiabetics for glucose metabolism disorders
Est. expirySep 17, 2018(expired)· nominal 20-yr term from priority
A61K 31/155A61K 31/555A61K 45/06A61P 3/08A61K 31/175A61P 3/10A61K 31/426A61K 33/24
68
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Claims
Abstract
Compositions and methods of using the same for the treatment of diabetes and other disorders of glucose metabolism are provided. Compositions may include an anti-diabetic agent and one or more of a bioavailable source of chromium and vanadium.
Claims
exact text as granted — not AI-modified1 - 96 . (canceled)
97 . A composition comprising synergistic effective amounts of an anti-diabetic agent other than insulin and a bioavailable source of vanadium, wherein said anti-diabetic agent is metformin, and wherein components of said composition synergistically reduce the HbA1c levels of a patient by at least about 10% after treatment for a period of at least about thirty days with said composition as compared to treatment with said anti-diabetic agent alone.
98 . The composition of claim 97 , wherein said reduction in said Hb1Ac level is at least about 50%.
99 . The composition of claim 97 , wherein said bioavailable source of vanadium is vanadyl sulfate.
100 . The composition of claim 99 , wherein the amount of vanadyl sulfate is in the range of about 20 mg up to about 100 mg per dose.
101 . The composition of claim 97 , wherein said bioavailable source of vanadium comprises more than about 10 mg elemental vanadium.
102 . The composition of claim 97 , wherein said amount of said bioavailable source of vanadium comprises no less than 5 mg of elemental vanadium.
103 . A method for improving glucose metabolism, comprising treating a patient for at least about a thirty day period by administering a pharmaceutical composition comprising synergistic effective amounts of an anti-diabetic agent other than insulin and a bioavailable source of vanadium, wherein said anti-diabetic agent is metformin, and wherein said components of said composition synergistically reduce the HbA1c level of said patient by at least about 10% after such treatment as compared to treatment with said anti-diabetic agent alone.
104 . The method of claim 103 , wherein said bioavailable source of vanadium comprises at least about 10 mg elemental vanadium when said composition is administered on a daily basis.
105 . The method of claim 103 , wherein said bioavailable source of vanadium is vanadyl sulfate.
106 . The method of claim 103 , wherein said amount of said bioavailable source of vanadium comprises no less than 5 mg of elemental vanadium when said composition is administered on a daily basis.
107 . The method of claim 103 , wherein said pharmaceutical composition further comprises a physiologically acceptable carrier.
108 . The method of claim 103 , wherein said method further comprises monitoring said subject's HbA1c levels.
109 . The method of claim 103 , wherein said reduction in said Hb1Ac level is at least about 50%.Join the waitlist — get patent alerts
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