Pharmaceutical composition containing FLT3 inhibitor and chemotherapeutic agent for treating acute myelogenous leukemia
An acute myeloid system and composition technology, applied in the direction of drug combinations, medical preparations containing active ingredients, pharmaceutical formulas, etc., can solve problems such as poor prognosis and limited long-term curative effect
Pending Publication Date: 2022-06-21
HANMI PHARMA
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Problems solved by technology
In addition, with conventional acute myeloid leukemia (AML) standard chemotherapy, targeting AML stem / progenitor cells is impossible, so the disease often recurs in patients, and thus there is a problem of limited long-term efficacy (Non-Patent Document 2)
Treatment of FLT3- AML patients with ITD mutations also exhibit poorer prognosis (Non-Patent Document 4)
Method used
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[0151] MV-4-11 cell line xenograft mouse model
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Abstract
Provided are pharmaceutical compositions for the treatment of acute myelogenous leukemia (AML); and a method for treating acute myelogenous leukemia by using the pharmaceutical composition. The pharmaceutical composition comprises a therapeutically effective combination of: an Fms-like tyrosine kinase-3 (FLT3) inhibitor, or a pharmaceutically acceptable salt or solvate thereof; and a chemotherapeutic agent or a pharmaceutically acceptable salt or solvate thereof.
Description
technical field [0001] The present invention relates to pharmaceutical compositions for the treatment of acute myeloid leukemia comprising effective therapeutic compositions of Fms-like tyrosine kinase-3 (FLT3) inhibitors and chemotherapeutic agents; and methods of treatment using such compositions. Background technique [0002] Fms-like tyrosine kinase-3 (FLT3) is one of the most commonly mutated genes in acute myeloid leukemia (AML). Mutant FLT3 (mutant FLT3) refers to a mutation expressed in leukemia cells present in a subset of acute myeloid leukemia (AML) patients. Activating mutations in FLT3, such as intragenic tandem duplication (ITD) in the proximal domain, appear in about 25-30% of newly diagnosed AML cases (Patent Document 1). FLT3 mutation is known to occur in about one-third of acute myeloid leukemia (AML) patients (Non-Patent Document 1). [0003] Although several FLT3 inhibitors are clinically available, drug-resistant leukocytes have been observed in AML pa...
Claims
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Patent Type & Authority Applications(China)
IPC IPC(8): A61K31/506A61K31/496A61K45/06A61P35/02
CPCA61K31/506A61P35/02A61K45/06A61K31/00A61K31/496A61K2300/00
Inventor 裵仁焕宋芝英崔载律安永吉
Owner HANMI PHARMA
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