Treatment of cancer with 2-deoxyglucose
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1. A method of treating cancer in a human cancer patient, which method comprises administering to said patient a therapeutically effective dose of 2-deoxy-D-glucose (2-DG), said therapeutically effective dose obtained by orally administering 2-DG daily to said patient in a range of about 25 mg of 2-DG per kg of patient weight to about 150 mg of 2-DG per kg of patient weight for at least five consecutive days.
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Abstract
The compound 2-deoxyglucose can be used to treat cancer and to improve patient outcome when administered at a therapeutically effective dose, and, optionally, co-administered with other anti-cancer drugs, or in combination with surgical resection or radiation therapy.
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17 Claims
- 1. A method of treating cancer in a human cancer patient, which method comprises administering to said patient a therapeutically effective dose of 2-deoxy-D-glucose (2-DG), said therapeutically effective dose obtained by orally administering 2-DG daily to said patient in a range of about 25 mg of 2-DG per kg of patient weight to about 150 mg of 2-DG per kg of patient weight for at least five consecutive days.
- 7. A method of treating a human cancer patient, which method comprises administering to said patient a therapeutically effective dose of 2-DG in combination with another anti-cancer agent, wherein the therapeutically effective dose of 2-DG is obtained by orally administering 2-DG daily in a range of about 25 mg of 2-DG per kg of patient weight to about 150 mg of 2-DG per kg of patient weight for at least five consecutive days.
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14. A method of treating cancer in a human patient having a solid tumor, which method comprises administering to said patient a therapeutically effective dose of 2-deoxy-D-glucose (2-DG), said therapeutically effective dose obtained by orally administering 2-DG daily in a range of about 25 mg of 2-DG per kg of patient weight to about 150 mg of 2-DG per kg of patient weight for at least five consecutive days.
- 15. A method of treating cancer in a human cancer patient, which method comprises co-administering to said patient (i) a therapeutically effective dose of 2-deoxy-D-glucose (2-DG), said therapeutically effective dose obtained by orally administering 2-DG daily in a range of about 25 mg of 2-DG per kg of patient weight to about 150 mg of 2-DG per kg of patient weight for at least five consecutive days, and (ii) an anti-cancer agent selected from the group consisting of docetaxel, paclitaxel, cisplatin, and carboplatin.
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