US2007293566A1PendingUtilityA1
Combinations of vanadium with antidiabetics for glucose metabolism disorders
Est. expirySep 17, 2018(expired)· nominal 20-yr term from priority
A61P 3/08A61P 3/10A61K 31/175A61K 31/155A61K 31/555A61K 31/426A61K 45/06A61K 33/24
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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 a sulfonylurea; and said composition synergistically reduces 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 bioavailable source of vanadium is vanadyl sulfate.
99 . The composition of claim 98 , wherein the amount of vanadyl sulfate is in the range of about 20 mg up to about 100 mg, per dose.
100 . The composition of claim 97 , wherein said bioavailable source of vanadium comprises more than about 10 mg elemental vanadium.
101 . The composition of claim 97 , wherein said amount of said bioavailable source of vanadium comprises no less than 5 mg of elemental vanadium.
102 . The composition according to claim 97 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, tolbutamide, glycazide, glipizide, glyburide, and glimeperide.
103 . The composition according to claim 97 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, and tolbutamide.
104 . The composition according to claim 97 , wherein said sulfonylurea is selected from the group consisting of glycazide, glipizide, glyburide, and glimeperide.
105 . The composition according to claim 97 , wherein said sulfonylurea is glyburide.
106 . The composition according to claim 97 , wherein said sulfonylurea is glipizide.
107 . The composition according to claim 97 , wherein said sulfonylurea is glimeperide.
108 . The composition according to claim 98 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, tolbutamide, glycazide, glipizide, glyburide, and glimeperide.
109 . The composition according to claim 98 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, and tolbutamide.
110 . The composition according to claim 98 , wherein said sulfonylurea is selected from the group consisting of glycazide, glipizide, glyburide, and glimeperide.
111 . The composition according to claim 98 , wherein said sulfonylurea is glyburide.
112 . The composition according to claim 98 , wherein said sulfonylurea is glipizide.
113 . The composition according to claim 98 , wherein said sulfonylurea is glimeperide.
114 . A method for improving glucose metabolism, comprising the step of co-administering to a patient for at least about thirty days synergistic effective amounts of an anti-diabetic agent other than insulin and a bioavailable source of vanadium, wherein said anti-diabetic agent is a sulfonylurea; and said anti-diabetic agent and bioavailable source of chromium 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.
115 . The method of claim 114 , wherein said bioavailable source of vanadium comprises at least about 10 mg elemental vanadium when said composition is administered on a daily basis.
116 . The method of claim 114 , 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.
117 . The method of claim 114 , wherein said bioavailable source of vanadium is vanadyl sulfate.
118 . The method of claim 114 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, tolbutamide, glycazide, glipizide, glyburide, and glimeperide.
119 . The method of claim 114 , wherein said sulfonylurea is selected from the group consisting of glycazide, glipizide, glyburide, and glimeperide.
120 . The method of claim 114 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, and tolbutamide.
121 . The method of claim 114 , wherein said sulfonylurea is glyburide.
122 . The method of claim 114 , wherein said sulfonylurea is glipizide.
123 . The method of claim 114 , wherein said sulfonylurea is glimeperide.
124 . The method of claim 117 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, tolbutamide, glycazide, glipizide, glyburide, and glimeperide.
125 . The method of claim 117 , wherein said sulfonylurea is selected from the group consisting of glycazide, glipizide, glyburide, and glimeperide.
126 . The method of claim 117 , wherein said sulfonylurea is selected from the group consisting of acetohexamide, chlorpropamide, tolazamide, and tolbutamide.
127 . The method of claim 117 , wherein said sulfonylurea is glyburide.
128 . The method of claim 117 , wherein said sulfonylurea is glipizide.
129 . The method of claim 117 , wherein said sulfonylurea is glimeperide.
130 . The method of claim 114 , wherein said sulfonylurea and bioavailable source of vanadium are comprised by a pharmaceutical composition further comprising a physiologically acceptable carrier.
131 . The method of claim 114 , further comprising the step of monitoring said subject's HbA1c levels.
132 . The method of claim 114 , wherein said reduction in said Hb1Ac level is at least about 50%.Join the waitlist — get patent alerts
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