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US 2002/0177602 A1Published application
Antidiabetic formulation and method
AssigneeBristol-Myers Squibb Company
InventorBETH ANNE PIPER
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AssigneeBristol-Myers Squibb Company
InventorBETH ANNE PIPER
Estimating the term…
A low dose antidiabetic pharmaceutical formulation is provided, especially adapted for treating Type II diabetes in drug naive patients, which includes a combination of metformin (employed in a reduced amount (less than 800 mg metformin per day) compared to that employed in generally accepted medical practice) and at least one other antidiabetic agent such as a sulfonyl urea, for example, glyburide, which combination provides at least about substantially equivalent efficacy in treating diabetes in drug naive patients, as do antidiabetic formulations containing metformin employed in dosages prescribed in generally accepted medical practice for first line therapy in treating diabetes, but with substantially reduced side effects, such as hypoglycemia and/or gastrointestinal distress. A method for treating diabetes in drug naive human patients is also provided employing the above formulation to reduce insulin resistance and/or post-prandial glucose excursion and/or hemoglobin 1Ac, and/or increase post-prandial insulin, thereby treating the diabetes.
A low dose pharmaceutical formulation for first line treatment of diabetes in drug naive patients comprising a low dose combination of metformin and at least one other antidiabetic agent, which provides at least substantially equivalent efficacy in treating diabetes in drug naive patients, but with substantially reduced side effects, as compared to combinations of metformin and the other antidiabetic agent, employed in substantially higher daily dosages as prescribed in generally accepted medical practice for first line therapy in treating diabetes.
A low dose pharmaceutical formulation for first line treatment of diabetes in drug naive patients comprising a low dose combination of metformin and glyburide, which provides at least substantially equivalent efficacy in treating diabetes in drug naive patients, but with substantially reduced side effects, as compared to combinations of metformin and glyburide employed in substantially higher daily dosages as prescribed in generally accepted medical practice for first line therapy in treating diabetes.
A method for first line treatment of type 2 diabetes in a drug naive human patient, which comprises administering to a drug naive human patient in need of treatment, as first line therapy, a therapeutically effective low dose of a pharmaceutical formulation comprising a low dose combination of metformin and at least one other antidiabetic agent, which provides at least substantially equivalent efficacy in treating diabetes in drug naive patients, but with substantially reduced side effects, as compared to metformin and said other antidiabetic agent employed in substantially higher daily dosages as prescribed in generally accepted medical practice for first line therapy in treating diabetes.
A method for first line treatment of type 2 diabetes, in a drug naive human patient, which comprises administering to a drug naive human patient in need of treatment, as first line therapy, a therapeutically effective low dose of a combination of metformin and glyburide which provides at least equivalent efficacy in treating diabetes in drug naive patients, but with substantially reduced side effects, as do combinations of metformin and said glyburide employed in substantially higher daily dosages as prescribed in generally accepted medical practice for first line therapy in treating diabetes.
Dependencies are inferred from the claim text.