IP Library Granted Patent US 8,383,607
Granted Patent B2
US 8,383,607 · App. 13/077,766 · Granted Feb 26, 2013

Perifosine and capecitabine as a combined treatment for cancer

Inventors: Enrique Poradosu (Brookline, MA); Peeter Sportelli (North Andover, MA)
Assignee: AEterna Zentaris GmbH
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Quick Facts
Patent No.
US 8,383,607
App. No.
13/077,766
Granted
Feb 26, 2013
Kind
B2
Abstract

Treatment regimens comprising co-treatment of cancer with perifosine and capecitabine are disclosed herein, as well as pharmaceutical compositions and unit dosage forms thereof formulated to be suitable for use in said treatment regimens.

Claims (25)

1. A method for treating metastatic colorectal cancer which is characterized by a resistance to a chemotherapeutic agent, comprising administering to a human subject in need thereof 50 mg of perifosine per day and 2000 mg/m 2 of capecitabine per day, wherein the perifosine is administered every day and the capecitabine is administered on days 1 to 14 of a 21 day cycle.

2. A method for treating metastatic colorectal cancer which is characterized by a resistance to a fluoropyrimidine, comprising administering to a human subject in need thereof 50 mg of perifosine per day and 2000 mg/m 2 of capecitabine per day, wherein the perifosine is administered every day and the capecitabine is administered on days 1 to 14 of a 21 day cycle.

3. A method for treating metastatic colorectal cancer which is characterized by a resistance to 5-fluorouracil, comprising administering to a human subject in need thereof 50 mg of perifosine per day and 2000 mg/m 2 of capecitabine per day, wherein the perifosine is administered every day and the capecitabine is administered on days 1 to 14 of a 21 day cycle.

4. A method for treating metastatic colorectal cancer in a human subject characterized as intolerant to a prior chemotherapeutic agent, comprising administering to the human subject 50 mg of perifosine per day and 2000 mg/m 2 of capecitabine per day, wherein the perifosine is administered every day and the capecitabine is administered on days 1 to 14 of a 21 day cycle.

5. A method for treating metastatic colorectal cancer in a human subject characterized as intolerant to a 5-fluorouracil, comprising administering to the human subject 50 mg of perifosine per day and 2000 mg/m 2 of capecitabine per day, wherein the perifosine is administered every day and the capecitabine is administered on days 1 to 14 of a 21 day cycle.

6. A method for treating metastatic colorectal cancer in a human subject previously treated with an anti-epidermal growth factor receptor antibody, comprising administering to the human subject 50 mg of perifosine per day and 2000 mg/m 2 of capecitabine per day, wherein the perifosine is administered every day and the capecitabine is administered on days 1 to 14 of a 21 day cycle.

7. The method of claim 1 , wherein the chemotherapeutic agent is paclitaxel, an anthracycline, irinotecan, oxaliplatin, bevacizumab, or an anti-epidermal growth factor receptor antibody.

8. The method of claim 7 , wherein the anti-epidermal growth factor receptor antibody is cetuximab or panitumumab.

9. The method of claim 2 , wherein the fluoropyrimidine is floxuridine, tegafur or capecitabine.

10. The method of claim 4 , wherein the chemotherapeutic agent is paclitaxel, an anthracycline, a fluoropyrimidine, irinotecan, oxaliplatin, bevacizumab, or an anti-epidermal growth factor receptor antibody.

11. The method of claim 10 , wherein the fluoropyrimidine is 5-fluorouracil, floxuridine, tegafur or capecitabine.

12. The method of claim 10 , wherein the anti-epidermal growth factor receptor antibody is cetuximab or panitumumab.

13. The method of claim 10 , wherein the anti-epidermal growth factor receptor antibody is cetuximab or panitumumab.

14. The method of claim 1 , wherein the capecitabine is administered twice per day at a dosage of 1000 mg/m 2 on days 1 to 14 of a 21 day cycle.

15. The method of claim 2 , wherein the capecitabine is administered twice per day at a dosage of 1000 mg/m 2 on days 1 to 14 of a 21 day cycle.

16. The method of claim 3 , wherein the capecitabine is administered twice per day at a dosage of 1000 mg/m 2 on days 1 to 14 of a 21 day cycle.

17. The method of claim 4 , wherein the capecitabine is administered twice per day at a dosage of 1000 mg/m 2 on days 1 to 14 of a 21 day cycle.

18. The method of claim 5 , wherein the capecitabine is administered twice per day at a dosage of 1000 mg/m 2 on days 1 to 14 of a 21 day cycle.

19. The method of claim 6 , wherein the capecitabine is administered twice per day at a dosage of 1000 mg/m 2 on days 1 to 14 of a 21 day cycle.

20. The method of claim 1 , wherein the perifosine and capecitabine are orally administered.

21. The method of claim 2 , wherein the perifosine and capecitabine are orally administered.

22. The method of claim 3 , wherein the perifosine and capecitabine are orally administered.

23. The method of claim 4 , wherein the perifosine and capecitabine are orally administered.

24. The method of claim 5 , wherein the perifosine and capecitabine are orally administered.

25. The method of claim 6 , wherein the perifosine and capecitabine are orally administered.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2012
From: KERYX BIOPHARMACEUTICALS, INC.
To: AETERNA ZENTARIS GMBH
Reel/Frame 028877/0699 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2011
From: PORADOSU, ENRIQUE; SPORTELLI, PETER
To: KERYX BIOPHARMACEUTICALS, INC.
Reel/Frame 026431/0724 →
Continuity (2)
Provisional Application 61319315 · Mar 31, 2011
Related Publication 20110243933A1 · Oct 6, 2011