IP Library Granted Patent US 8,673,321
Granted Patent B2
US 8,673,321 · App. 13/230,212 · Granted Mar 18, 2014

Cyclophosphamide in combination with anti-idiotypic vaccines

Inventors: Robert A. Brodsky (Brooklandville, MD); Richard J. Jones (Baltimore, MD); Francis E. O'Donnell, Jr. (Town and Country, MO); Susan Bonitz (Flemington, NJ); Carlos Santos (Tampa, FL)
Assignees: The Johns Hopkins University; Accentia Biopharmaceuticals, Inc.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,673,321
App. No.
13/230,212
Granted
Mar 18, 2014
Kind
B2
Abstract

The present invention relates to methods of treating a cancer and in particular, a B-cell derived cancer, using a lymphocytotoxic but hematopoeitic cell sparing high-dose pulsed amount of an oxazaphosphorine drug in combination with immune therapeutics such as, for example, an autologous idiotypic vaccine and monoclonal antibodies that selectively bind B-cell specific antigens.

Claims (26)

1. A method for eliminating or substantially reducing a B-cell derived cancer in a subject comprising administering a lymphocytotoxic but hematopoietic stem cell sparing high-dose pulsed amount of an oxazaphosphorine drug to the subject, such that the subject's immune system reconstitutes without stem cell transplantation, administering to the subject one or more monoclonal antibodies that selectively bind to a B-cell specific antigen, and administering an effective amount of an autologous anti-idiotypic vaccine, thereby to eliminate or substantially reduce the B-cell derived cancer in the subject.

2. The method of claim 1 , wherein the B-cell derived cancer is selected from the group consisting of non-Hodgkin's lymphoma, Hodgkin's lymphoma, mantle cell lymphoma, chronic lymphocytic leukemia and multiple myeloma.

3. The method of claim 1 , wherein the autologous anti-idiotypic vaccine is administered in conjunction with an effective amount of granulocyte-monocyte colony stimulating factor.

4. The method of claim 1 , wherein the B-cell specific antigen is selected from the group consisting of CD3d, CD5, CD6, CD9, CD19, CD20, CD21, CD22, CD23, CD24, CD27, CD28, CD37, CD38, CD40, CD45, CD46, CD48, CD53, CD69, CD70, CD72, CD73, CD79a, CD79b, CD80, CD81, CD83, CD85a, CD85d, CD85e, CD85h, CD85i, CD85j, CD85k, CD86, CD96, CD98, CD100, CD121b, CD124, CD127, CD132, CD150, CD152, CD154, CD157, CD166, CD169, CD179a, CD179b, CD180, CD185, CD196, CD197, CD205, CDw210a, CD213a1, CD257, CD267, CD268, CD269, CD274, CD275, CD276, CD278, CD279, CD300a, CD300c, CD307, CD314, CD316, CD317, CD319, CD320, CDw327, and CD331.

5. The method of claim 1 , wherein the one or more monoclonal antibodies selectively binds to CD-20.

6. The method of claim 1 , wherein the one or more monoclonal antibodies selectively binds to CD-22.

7. The method of claim 1 , wherein the amount of an oxazaphosphorine drug is 50 mg/kg/day.

8. The method of claim 1 , wherein the oxazaphosphorine drug is administered to the subject for 4 days.

9. The method of claim 1 , wherein the oxazaphosphorine drug administered to the subject at a dose of 50 mg/kg/day for 4 days.

10. The method of claim 1 , wherein the oxazaphosphorine drug is cyclophosphamide administered in the amount of 50 mg/Kg for 4 days.

11. The method of claim 1 , wherein the oxazaphosphorine drug is powdered cyclophosphamide or a pharmaceutically acceptable salt, solvate, prodrug, or metabolite thereof.

12. The method of claim 1 , wherein the oxazaphosphorine drug is lyophilized cyclophosphamide or a pharmaceutically acceptable salt, solvate, prodrug, or metabolite thereof.

13. The method of claim 1 , further comprising administering an effective amount of Mesna.

14. The method of claim 1 , wherein the autologous anti-idiotypic vaccine and the one or more monoclonal antibodies are administered after administration of the oxazaphosphorine drug.

15. A method of eliminating or substantially reducing a B-cell derived cancer selected from the group consisting of non-Hodgkin's lymphoma, Hodgkin's lymphoma, mantle cell lymphoma, chronic lymphocytic leukemia and multiple myeloma in a subject comprising administering to the subject: (a) a lymphocytotoxic but hematopoietic stem cell sparing high-dose pulsed amount of an oxazaphosphorine drug; (b) an effective amount of an autologous anti-idiotypic vaccine in conjunction with an effective amount of GM-CSF; and (c) an effective amount of one or more monoclonal antibodies that selectively bind one or more B-cell specific antigens, thereby eliminating or substantially reducing the B-cell derived cancer in the subject.

16. The method of claim 15 , wherein the autologous anti-idiotypic vaccine and the one or more monoclonal antibodies are administered after administration of the oxazaphosphorine drug.

17. The method of claim 15 , wherein the B-cell specific antigen is selected from the group consisting of CD3d, CD5, CD6, CD9, CD19, CD20, CD21, CD22, CD23, CD24, CD27, CD28, CD37, CD38, CD40, CD45, CD46, CD48, CD53, CD69, CD70, CD72, CD73, CD79a, CD79b, CD80, CD81, CD83, CD85a, CD85d, CD85e, CD85h, CD85i, CD85j, CD85k, CD86, CD96, CD98, CD100, CD121b, CD124, CD127, CD132, CD150, CD152, CD154, CD157, CD166, CD169, CD179a, CD179b, CD180, CD185, CD196, CD197, CD205, CDw210a, CD213a1, CD257, CD267, CD268, CD269, CD274, CD275, CD276, CD278, CD279, CD300a, CD300c, CD307, CD314, CD316, CD317, CD319, CD320, CDw327, and CD331.

18. The method of claim 15 , wherein the one or more monoclonal antibodies selectively binds to CD-20.

19. The method of claim 15 , wherein the one or more monoclonal antibodies selectively binds to CD-22.

20. The method of claim 15 , wherein the amount of an oxazaphosphorine drug is 50 mg/kg/day.

21. The method of claim 15 , wherein the oxazaphosphorine drug is administered to the subject for 4 days.

22. The method of claim 15 , wherein the oxazaphosphorine drug administered to the subject at a dose of 50 mg/kg/day for 4 days.

23. The method of claim 15 , wherein the oxazaphosphorine drug is cyclophosphamide administered in the amount of 50 mg/Kg for 4 days.

24. The method of claim 15 , wherein the oxazaphosphorine drug is powdered cyclophosphamide or a pharmaceutically acceptable salt, solvate, prodrug, or metabolite thereof.

25. The method of claim 15 , wherein the oxazaphosphorine drug is lyophilized cyclophosphamide or a pharmaceutically acceptable salt, solvate, prodrug, or metabolite thereof.

26. The method of claim 15 , further comprising administering an effective amount of Mesna.

Assignments (3)
CERTIFICATE OF TITLE Recorded Oct 21, 2014
From: ACCENTIA BIOPHARMACEUTICALS, INC.
To: PABETI, INC.
Reel/Frame 034029/0770 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2012
From: BRODSKY, ROBERT A.; JONES, RICHARD J.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 027836/0419 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2012
From: O'DONNELL, FRANCIS E.; BONITZ, SUSAN; SANTOS, CARLOS
To: ACCENTIA BIOPHARMACEUTICALS, INC.
Reel/Frame 027836/0446 →
Continuity (7)
Continuation 13017817 · Jan 31, 2011
Continuation 12818380 · Jun 18, 2010
Continuation 12610798 · Nov 2, 2009
Continuation 12404891 · Mar 16, 2009
Continuation PCTUS2007078521 · Sep 14, 2007
Provisional Application 60844830 · Sep 15, 2006
Related Publication 20120148611A1 · Jun 14, 2012