US2014017315A1PendingUtilityA1

Methods and compositions for treeating proliferative diseases

Assignee: ABRAXIS BIOSCIENCE LLCPriority: Feb 18, 2005Filed: Feb 25, 2013Published: Jan 16, 2014
Est. expiryFeb 18, 2025(expired)· nominal 20-yr term from priority
A61P 43/00A61P 35/00A61P 35/04A61P 9/08A61P 9/10A61P 15/00A61P 17/06A61P 11/00A61K 31/517A61K 31/7068A61K 45/06A61K 31/337A61K 38/16A61K 31/17A61K 31/519A61K 9/0019A61K 2300/00A61K 31/5377A61K 31/675A61K 31/436A61K 47/6931A61K 47/643A61K 47/42A61K 9/146A61K 31/7072A61K 31/165A61K 9/5169A61K 31/69A61K 31/555A61K 39/39558A61K 31/282A61K 31/704A61N 5/10A61K 2121/00A61K 38/38B82Y 5/00A61K 51/10A61K 31/395A61K 33/243
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Claims

Abstract

The present invention provides combination therapy methods of treating proliferative diseases (such as cancer) comprising a first therapy comprising administering to an individual an effective amount of a taxane in a nanoparticle composition, and a second therapy which may include, for example, radiation, surgery, administration of chemotherapeutic agents, or combinations thereof. Also provided are methods of administering to an individual a drug taxane in a nanoparticle composition based on a metronomic dosing regime.

Claims

exact text as granted — not AI-modified
1 - 16 . (canceled) 
     
     
         17 . A method of treating a proliferative disease in an individual comprising administering to the individual:
 a) an effective amount of a composition comprising nanoparticles comprising a taxane and an albumin, and   b) an effective amount of at least one other chemotherapeutic agent, wherein said chemotherapeutic agent is selected from the group consisting of antimetabolites, platinum-based agents, alkylating agents, tyrosine kinase inhibitors, anthracycline antibiotics, vinca alkloids, proteasome inhibitors, macrolides, and topoisomerase inhibitors.   
     
     
         18 . The method according to  claim 17 , wherein said chemotherapeutic agent is an antimetabolite agent. 
     
     
         19 . The method according to  claim 18 , wherein said chemotherapeutic agent is a platinum-based agent. 
     
     
         20 . The method according to  claim 17 , wherein said chemotherapeutic agent is a tyrosine kinase inhibitor. 
     
     
         21 . The method according to  claim 17 , wherein the proliferative disease is cancer. 
     
     
         22 . The method according to  claim 17 , wherein the taxane is paclitaxel. 
     
     
         23 . The method according to  claim 22 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm. 
     
     
         24 . The method according to  claim 17 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm. 
     
     
         25 . The method according to  claim 17 , wherein the individual is a human. 
     
     
         26 . A method of treating a tumor in an individual comprising:
 a) a first therapy comprising administering to the individual an effective amount of a composition comprising nanoparticles comprising a taxane and an albumin, and   b) a second therapy comprising radiation therapy, surgery, or combinations thereof.   
     
     
         27 . The method according to  claim 26 , wherein the taxane is paclitaxel. 
     
     
         28 . The method according to  claim 27 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm. 
     
     
         29 . The method according to  claim 26 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm. 
     
     
         30 . The method according to  claim 26 , wherein the individual is a human. 
     
     
         31 . A method of administering a composition comprising nanoparticles comprising a taxane and an albumin to an individual,
 wherein the nanoparticle composition is administered over a period of at least one month, wherein the interval between each administration is no more than about a week, and   wherein the dose of taxane in the composition at each administration is about 0.25% to about 25% of its maximum tolerated dose following a traditional dosing regime.   
     
     
         32 . The method according to  claim 31 , wherein said taxane is paclitaxel. 
     
     
         33 . The method according to  claim 32 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm. 
     
     
         34 . The method according to  claim 31 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm. 
     
     
         35 . The method according to  claim 31 , wherein the individual is a human.

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