IP Library Patent Application 14912077
Patent Application
App. No. 14/912,077

CANCER TREATMENT

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Quick Facts
Patent No.
US None
App. No.
14/912,077
Filed
Feb 12, 2016
Art Unit
1673
USPC
514/574
Abstract

The invention relates generally to the treatment of cancer. One embodiment of the invention provides a method of treating cancer in an individual, the method comprising: administering to the individual an effective amount of trichostatin A (TSA).

Claims (30)

1 . A method of treating cancer in an individual, the method comprising:

administering to the individual an effective amount of trichostatin A (TSA).

2 . The method of claim 1 , wherein the effective amount is an amount sufficient to decrease an aurora kinase A (AURKA) level in the individual.

3 . The method of claim 1 , wherein the effective amount is an amount sufficient to inhibit histone deacetylase (HDAC) activity and decrease an aurora kinase A (AURKA) level in the individual.

4 . The method of claim 1 , wherein the effective amount is between about 0.1 mg/kg/day and about 10 mg/kg/day.

5 . The method of claim 4 , wherein the effective amount is between about 0.5 mg/kg/day and about 5 mg/kg/day.

6 . The method of claim 5 , wherein TSA is the only AURKA inhibitor administered to the individual.

7 . The method of claim 1 , wherein the cancer includes at least one cancer selected from a group consisting of: breast cancer, gastric cancer, colon cancer, rectal cancer, bladder cancer, pancreatic cancer, ovarian cancer, prostate cancer, lung cancer, hematological cancer, skin cancer, and malignancies.

8 . The method of claim 1 , wherein administering includes orally administering.

9 . The method of claim 1 , wherein administering includes intravenously administering.

10 . A method of treating a cancer in an individual, the method comprising:

determining, from a tumor sample obtained from the individual's body, a level of aurora kinase A (AURKA) expression; and

in the case that the level of AURKA expression is indicative of overexpression, administering to the individual an effective amount of trichostatin A (TSA).

11 . The method of claim 10 , wherein the effective amount is an amount sufficient to decrease an aurora kinase A (AURKA) level in the individual.

12 . The method of claim 10 , wherein the effective amount is an amount sufficient to inhibit histone deacetylase (HDAC) activity and decrease an aurora kinase A (AURKA) level in the individual.

13 . The method of claim 10 , wherein the effective amount is between about 0.1 mg/kg/day and about 10 mg/kg/day.

14 . The method of claim 13 , wherein the effective amount is between about 0.5 mg/kg/day and about 5 mg/kg/day.

15 . The method of claim 10 , wherein TSA is the only AURKA inhibitor administered to the individual.

16 . The method of claim 10 , wherein the cancer includes at least one cancer selected from a group consisting of: breast cancer, gastric cancer, colon cancer, rectal cancer, bladder cancer, pancreatic cancer, ovarian cancer, prostate cancer, lung cancer, hematological cancer, skin cancer, and malignancies.

17 . The method of claim 10 , wherein administering includes orally administering.

18 . The method of claim 10 , wherein administering includes intravenously administering.

19 . A pharmaceutical composition comprising:

trichostatin A (TSA) as a sole or primary aurora kinase A (AURKA) inhibitor; and

a pharmaceutically-acceptable excipient or carrier.

20 . The pharmaceutical composition of claim 19 formulated for oral administration.

21 . The pharmaceutical composition of claim 19 formulated for intravenous administration.

22 . The pharmaceutical composition of claim 19 , comprising TSA in an amount between about 1 mg and about 500 mg.

23 . The pharmaceutical composition of claim 22 , wherein the amount of TSA is equivalent to a dose between about 0.1 mg/kg/day and about 10 mg/kg/day.

24 . The pharmaceutical composition of claim 23 , wherein the amount of TSA is equivalent to a dose between about 0.5 mg/kg/day and about 5 mg/kg/day.

25 . The pharmaceutical composition of claim 22 , wherein the amount of TSA is effective to inhibit histone deacetylase (HDAC) activity.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2016
From: POLYMEROPOULOS, MIHAEL H.; LICAMELE, LOUIS WILLIAM; LAVEDAN, CHRISTIAN
To: VANDA PHARMACEUTICALS, INC.
Reel/Frame 038167/0475 →