US2013195922A1PendingUtilityA1
Methods and compositions for treating proliferative diseases
Est. expiryFeb 18, 2025(expired)· nominal 20-yr term from priority
A61P 9/08A61P 35/04A61P 35/00A61P 9/10A61P 43/00A61P 17/06A61P 15/00A61P 11/00A61K 38/16A61K 31/555A61K 31/519A61K 47/643A61K 9/146A61K 31/165A61K 31/7068A61K 2300/00A61K 38/38A61K 2121/00A61K 47/42A61K 31/704A61K 31/5377A61K 31/436A61K 31/675A61K 31/337A61K 9/0019A61N 5/10A61K 31/69A61K 45/06A61K 9/5169A61K 39/39558A61K 31/7072A61K 31/517B82Y 5/00A61K 31/17A61K 47/6931A61K 31/282A61K 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-modifiedWhat is claimed is:
1 . A method of treating a proliferative disease in an individual, comprising administering to the individual an effective amount of a composition comprising nanoparticles comprising a thiocolchicine or a derivative thereof and a carrier protein.
2 . The method according to claim 1 wherein the proliferative disease is cancer.
3 . The method according to claim 2 , wherein the cancer is breast cancer.
4 . The method according to claim 2 , wherein the cancer is ovarian cancer.
5 . The method according to claim 1 , wherein the thiocolchicine or a derivative thereof is a dimeric thiocolchicine.
6 . The method according to claim 1 , wherein the dimeric thiocolchicine is IDN 5404, IDN5808, or IDN5801.
7 . The method according to claim 6 , wherein the dimeric thiocolchicine is IDN5404.
8 . The method according to claim 1 , wherein the thiocolchicine or a derivative thereof is administered intravenously.
9 . The method according to claim 1 , wherein the carrier protein is albumin.
10 . The method according to claim 9 , wherein the albumin is human serum albumin.
11 . The method according to claim 1 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm.
12 . The method according to claim 1 , wherein the individual is human.
13 . A method of treating cancer in an individual, comprising administering to the individual an effective amount of a composition comprising nanoparticles comprising rapamycin and a carrier protein.
14 . The method according to claim 13 , wherein the cancer is colon cancer.
15 . The method according to claim 13 , wherein the rapamycin is administered intravenously.
16 . A method of treating a proliferative disease in an individual, comprising administering to the individual an effective amount of a composition comprising nanoparticles comprising 17-AAG and a carrier protein.Cited by (0)
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