Methods of treating metastatic breast cancer with 4-iodo-3-nitrobenzamide and irinotecan
AssigneeBiPar Sciences, Inc.
InventorCharles Bradley
Life of this patent
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Abstract
Provided herein are methods, compositions and kits for the treatment of locally advanced or metastatic breast cancer or breast cancer brain metastases. The method comprises administration of 4-iodo-3-nitrobenzamide, a metabolite or salt thereof in combination with irinotecan. The method of treating locally advanced or metastatic breast cancer comprises at least one 21 day treatment cycle.
Claims38
A method of treating a patient with breast cancer brain metastasis comprising administering to the patient an effective amount of (a) 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof and (b) irinotecan or a pharmaceutically acceptable salt thereof, wherein the breast cancer is ER-negative, PR-negative, and HER2-nonoverexpressing.
A method of treating locally advanced or metastatic breast cancer in a patient, comprising administering to the patient having locally advanced or metastatic breast cancer an effective amount of (a) 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, and (b) irinotecan or a pharmaceutically acceptable salt thereof, wherein the method comprises at least one cycle, wherein the cycle is a period of 21 days, wherein 4-iodo-3-nitrobenzamide or the pharmaceutically acceptable salt thereof is administered at about 8 mg/kg twice weekly for two weeks of the cycle, and wherein irinotecan or a pharmaceutically acceptable salt thereof is administered at about 80 mg/m2 to about 125 mg/m2 once weekly for two weeks of the cycle.
A kit for treating a patient with breast cancer brain metastasis comprising (a) 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, and (b) irinotecan or a pharmaceutically acceptable salt thereof, wherein the breast cancer is ER-negative, PR-negative, and HER2-nonoverexpressing.
A kit comprising (a) 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, and (b) a package insert or label containing instructions for using an effective amount of 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, in combination with irinotecan or a pharmaceutically acceptable salt thereof to treat a patient with breast cancer brain metastasis, wherein the breast cancer is ER-negative, PR-negative, and HER2-nonoverexpressing.
A kit for treating locally advanced or metastatic breast cancer in a patient comprising (a) 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, (b) irinotecan or a pharmaceutically acceptable salt thereof, and (c) a package insert or label containing instructions for using 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, and irinotecan or a pharmaceutically acceptable salt thereof to treat locally advanced or metastatic breast cancer in the patient, wherein the treatment comprises at least one cycle, wherein the cycle is a period of 21 days, wherein 4-iodo-3-nitrobenzamide or the pharmaceutically acceptable salt thereof is administered at about 8 mg/kg twice weekly for two weeks of the cycle, and wherein irinotecan or a pharmaceutically acceptable salt thereof is administered at about 80 mg/m2 to about 125 mg/m2 once weekly for two weeks of the cycle.
A kit comprising (a) 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, and (b) a package insert or label containing instructions for using 4-iodo-3-nitrobenzamide or a metabolite thereof or a pharmaceutically acceptable salt thereof, in combination with irinotecan or a pharmaceutically acceptable salt thereof to treat locally advanced or metastatic breast cancer in a patient, wherein the treatment comprises at least one cycle, wherein the cycle is a period of 21 days, wherein 4-iodo-3-nitrobenzamide or the pharmaceutically acceptable salt thereof is administered at about 8 mg/kg twice weekly for two weeks of the cycle, and wherein irinotecan or a pharmaceutically acceptable salt thereof is administered at about 80 mg/m2 to about 125 mg/m2 once weekly for two weeks of the cycle.
Dependencies are inferred from the claim text.