IP Library Granted Patent US 8,318,683
Granted Patent B2
US 8,318,683 · App. 10/588,409 · Granted Nov 27, 2012

Anti-cancer therapies

Assignee: Threshold Pharmaceuticals, Inc.
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Quick Facts
Patent No.
US 8,318,683
App. No.
10/588,409
Granted
Nov 27, 2012
Kind
B2
Abstract

Methods for the treatment of cancer are described. In particular, methods for treatment of cancer comprising administration of glufosfamide alone or in combination with another anticancer agent are disclosed.

Claims (34)

1. A method of treating pancreatic cancer comprising administering glufosfamide and gemcitabine in combination to a subject in need of such treatment.

2. The method of claim 1 wherein the cancer is a locally advanced and/or metastatic solid tumor.

3. The method of claim 1 wherein glufosfamide is administered for one or more dosage cycles, each cycle comprising an infusion of glufosfamide in the range of:

a) about 1.5 to about 8.0 g/m 2 ; about 1.5 to about 6.0 g/m 2 ; about 1.5 to about 4.5 g/m 2 ;

about 4.5 to about 8.0 g/m 2 ; about 4.5 to about 6.0 g/m 2 ; or about 4.5 to about 5.0 g/m 2 or over an infusion period of 1-6 hours once every three weeks;

b) about 1.5 to about 3.0 g/m 2 or about 1.5 to about 2.0 g/m 2 over an infusion period of 1-6 hours for three consecutive days (days 1, 2 and 3) every three weeks;

c) about 1.5 to about 2.0 g/m 2 over an infusion period of 1-6 hours once per week; or

d) about 1.5 to about 8.0 g/m 2 ; about 1.5 to about 6.0 g/m 2 ; or about 1.5 to about 4.5 g/m 2 over an infusion period of 1-6 hours once every four weeks.

4. The method of claim 1 wherein gemcitabine is administered once each week of a seven-week dosage cycle, wherein said administration is for one or more seven-week cycles, and wherein each cycle comprises an infusion of gemcitabine of:

a) about 1000 mg/m 2 over a period of about 30 min;

b) about 2200 mg/m 2 over a period of about 30 min; or

c) about 1500 mg/m 2 over a period of about 150 min.

5. The method of claim 1 wherein gemcitabine is administered weeks 1, 2 and 3 of a four-week cycle for one more four-week cycles, and wherein each cycle comprises an infusion of gemcitabine of:

a) about 1000 mg/m 2 over a period of about 30 min;

b) about 2200 mg/m 2 over a period of about 30 min; or

c) about 1500 mg/m 2 over a period of about 150 min.

6. The method of claim 5 wherein each cycle comprises an infusion of glufosfamide in the range of about 1.5 to about 4.5 g/m 2 over an infusion period of 1-6 hours once every four weeks.

7. The method of claim 6 wherein gemcitabine is administered on the same day as the administration of glufosfamide.

8. The method of claim 7 wherein gemcitabine is administered between about 30 minutes to about 4 hours after the administration of glufosfamide.

9. A method of treating pancreatic cancer comprising administering glufosfamide and gemcitabine in combination to a subject in need of such treatment wherein glufosfamide is administered for one or more dosage cycles, each cycle comprising:

a) an infusion of glufosfamide in the range of about 1.5 to about 8.0 g/m 2 ; about 1.5 to about 6.0 g/m 2 ; or about 1.5 to about 4.5 g/m 2 over an infusion period of 1-6 hours once every four weeks; and

b) an infusion of gemcitabine of about 1000 mg/m 2 over a period of about 30 min.

10. The method of claim 9 wherein each cycle comprises an infusion of glufosfamide in the range of about 1.5 to about 4.5 g/m 2 over an infusion period of 1-6 hours once every four weeks.

11. The method of claim 9 wherein gemcitabine is administered on the same day as the administration of glufosfamide.

12. The method of claim 11 wherein gemcitabine is administered between about 30 minutes to about 4 hours after the administration of glufosfamide.

13. The method of claim 12 wherein glufosfamide is administered once every four weeks as an infusion in the range of about 1.5 to about 4.5 g/m 2 over an infusion period of 4 hours and gemcitabine is administered 30 minutes after the administration of glufosfamide.

14. A method of treating gemcitabine-refractory pancreatic cancer, comprising administering to a human subject in need thereof an effective amount of glufosfamide.

15. The method of claim 14 wherein glufosfamide is administered for one or more dosage cycles, each cycle comprising an infusion of glufosfamide in the range of:

a) about 1.5 to about 8.0 g/m 2 ; about 1.5 to about 6.0 g/m 2 ; about 1.5 to about 4.5 g/m 2 ; about 4.5 to about 8.0 g/m 2 ; about 4.5 to about 6.0 g/m 2 ; or about 4.5 to about 5.0 g/m 2 or over an infusion period of 1-6 hours once every three weeks;

b) about 1.5 to about 3.0 g/m 2 or about 1.5 to about 2.0 g/m 2 over an infusion period of 1-6 hours for three consecutive days (days 1, 2 and 3) every three weeks;

c) about 1.5 to about 2.0 g/m 2 over an infusion period of 1-6 hours once per week; or

d) about 1.5 to about 8.0 g/m 2 ; about 1.5 to about 6.0 g/m 2 ; or about 1.5 to about 4.5 g/m 2 over an infusion period of 1-6 hours once every four weeks.

16. The method of claim 14 , wherein glufosfamide is administered for one or more dosage cycles, each cycle comprising an infusion of glufosfamide in the range of about 1.5 to about 6.0 g/m 2 over an infusion period of 1-6 hours once every three weeks.

17. The method of claim 16 wherein each cycle comprises an infusion of about 4.5 g/m 2 glufosfamide over an infusion period of 1-6 hours once every three weeks.

Assignments (2)
CHANGE OF NAME Recorded May 7, 2020
From: THRESHOLD PHARMACEUTICALS, INC.
To: MOLECULAR TEMPLATES, INC.
Reel/Frame 052607/0818 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2008
From: TIDMARSH, GEORGE
To: THRESHOLD PHARMACEUTICALS, INC.
Reel/Frame 021011/0265 →
Continuity (2)
Provisional Application 60542494 · Feb 6, 2004
Related Publication 20090247480A1 · Oct 1, 2009