IP Library Granted Patent US 9,018,251
Granted Patent B2
US 9,018,251 · App. 13/109,619 · Granted Apr 28, 2015

Method for treating brain cancer or reducing temozolomide-resistance of brain cancer cells

Inventors: Horng-Jyh Harn (Taichung, TW); Shinn-Zong Lin (Taichung, TW); Tzyy-Wen Chiou (Taichung, TW); Po-Cheng Lin (Taichung, TW)
Assignee: China Medical University
A61K31/343A61K31/4188
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Quick Facts
Patent No.
US 9,018,251
App. No.
13/109,619
Granted
Apr 28, 2015
Kind
B2
Abstract

Provided is a method for treating brain cancer or reducing temozolomide-resistance of brain cancer cells in a subject, comprising administrating to the subject an effective amount of an active ingredient selected from the group consisting of (Z)-butylidenephthalide of formula (I), a pharmaceutically acceptable salt of (Z)-butylidenephthalide, a pharmaceutically acceptable ester of (Z)-butylidenephthalide, and combinations thereof:

Claims (9)

1. A method for treating a glioma in a subject, comprising:

administering to the subject (1) an effective amount of the (Z)-butylidenephthalide isomer of formula (I) substantially free from the (E)-butylidenephthalide isomer of formula (I), wherein the (Z)-butylidenephthalide isomer of formula (I) is in the form of the (Z)-butylidenephthalide isomer, a pharmaceutically acceptable salt of the (Z)-butylidenephthalide isomer, a pharmaceutically acceptable ester of the (Z)-butylidenephthalide isomer, or a combination thereof:

and (2) an effective amount of temozolomide, wherein (1) and (2) together provide a combination index less than 1.

2. The method as claimed in claim 1 , wherein the (Z)-butylidenephthalide isomer of formula (I) is in the form of the (Z)-butylidenephthalide isomer.

3. The method as claimed in claim 1 , wherein the glioma is human malignant glioma.

4. The method as claimed in claim 1 , wherein the (Z)-butylidenephthalide isomer of formula (I) is administrated in form of a wafer at a daily dosage of about 30 mg/kg-body weight to about 500 mg/kg-body weight, and temozolomide is administered as a wafer at a daily dosage of about 10 mg/kg-body weight to about 100 mg/kg-body weight.

5. The method as claimed in claim 4 , wherein the (Z)-butylidenephthalide isomer of formula (I) is administered at a daily dosage of about 40 mg/kg-body weight to about 120 mg/kg-body weight, and temozolomide is administrated at a daily dosage of about 40 mg/kg-body weight to about 80 mg/kg-body weight.

6. The method as claimed in claim 1 , wherein the (Z)-butylidenephthalide isomer of formula (I) and temozolomide are administered together, separately, or successively.

7. The method as claimed in claim 1 , wherein the (Z)-butylidenephthalide isomer of formula (I) is administered orally or administered by subcutaneous or intravenous injection and temozolomide is administered orally.

Assignments (2)
LICENSE Recorded Jan 22, 2025
From: CHINA MEDICAL UNIVERSITY; HARN, HORNG-JYH
To: EVERFRONT BIOTECH INC.
Reel/Frame 069962/0099 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2011
From: HARN, HORNG-JYH; LIN, SHINN-ZONG; CHIOU, TZYY-WEN; LIN, PO-CHENG
To: CHINA MEDICAL UNIVERSITY
Reel/Frame 026292/0915 →
Priority Claims (1)
TW 100100673 A · Jan 7, 2011 · national
Continuity (1)
Related Publication 20120178803A1 · Jul 12, 2012