US2021275453A1PendingUtilityA1

Tumor therapeutic agent and kit containing gemcitabine liposome composition

Assignee: FUJIFILM CORPPriority: Nov 2, 2015Filed: Feb 25, 2021Published: Sep 9, 2021
Est. expiryNov 2, 2035(~9.3 yrs left)· nominal 20-yr term from priority
A61K 9/127A61K 47/28A61K 47/24A61K 31/337A61K 31/7068A61P 35/00A61K 47/643A61K 45/06
66
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Claims

Abstract

An object of the present invention is to provide a tumor therapeutic agent and a kit which have superior antitumor effects as compared with gemcitabine, a taxane antitumor agent, and a combination therapy thereof which have been put on the market. According to the present invention, there is provided a tumor therapeutic agent obtained by combining a taxane antitumor agent with a liposome composition in which gemcitabine or a salt thereof is contained in a liposome.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of suppressing the growth of a human pancreatic cancer cell, comprising:
 administering a liposome composition in which gemcitabine or a salt thereof is contained in a liposome, and   administering nab-paclitaxel.   
     
     
         2 . The method according to  claim 1 , wherein a lipid forming the liposome contains hydrogenated soybean phosphatidylcholine, 1,2-distearoyl-3-phosphatidylethanolamine-polyethylene glycol, and cholesterol. 
     
     
         3 . The method according to  claim 1 , wherein the liposome is a single lamella. 
     
     
         4 . The method according to  claim 1 , wherein a release rate of gemcitabine or a salt thereof from the liposome composition in plasma is 10 mass %/24 hr to 70 mass %/24 hr. 
     
     
         5 . The method according to  claim 1 , wherein a content ratio of cholesterols to a total amount of the lipid forming the liposome is 10 mol % to 35 mol %, and an osmotic pressure of an inner aqueous phase of the liposome is 2 to 8 times an osmotic pressure of an outer aqueous phase of the liposome. 
     
     
         6 . The method according to  claim 1 , wherein an average particle diameter of the liposome is 2 nm to 200 nm.

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