US2021275453A1PendingUtilityA1
Tumor therapeutic agent and kit containing gemcitabine liposome composition
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-modifiedWhat 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.Join the waitlist — get patent alerts
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