IP Library Granted Patent US 10,668,151
Granted Patent B2
US 10,668,151 · App. 15/187,672 · Granted Jun 2, 2020

Nanoparticle complexes of albumin, paclitaxel, and panitumumab for treatment of cancer

Inventors: Svetomir N. Markovic (Rochester, MN); Wendy K. Nevala (Rochester, MN)
Assignee: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
A61K39/39558A61K9/0019A61K9/14A61K9/51A61K9/5169A61K31/282A61K31/337A61K31/555A61K33/24A61K39/395A61K41/0052A61K45/06A61K47/643A61K47/6801A61K47/6803A61K47/6845A61K47/6849A61K47/6851A61K47/6855A61K47/6863A61K47/6865A61K47/6867A61K47/6929A61K47/6931C07K16/22C07K16/2863C07K16/2887C07K16/2893C07K16/3015C07K16/32A61K2039/505A61K2039/545A61K2039/6056B82Y5/00C07K2317/21C07K2317/24C07K2317/73C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 10,668,151
App. No.
15/187,672
Granted
Jun 2, 2020
Kind
B2
Abstract

This invention relates to antibody-albumin nanoparticle complexes comprising albumin, an antibody with binding specificity for a cancer antigen (e.g. panitumumab), and paclitaxel, wherein the nanoparticle complex has been pre-formed in vitro such that the nanoparticle complex has antigen-binding specificity (e.g. EGFR binding specificity), for the purpose of providing cancer (e.g. EGFR-related cancer) treatments in a subject in need thereof.

Claims (17)

1. An antibody-albumin nanoparticle complex comprising albumin, a panitumumab antibody, and paclitaxel, wherein the nanoparticle complex has been pre-formed in vitro by mixing an aqueous albumin-paclitaxel nanoparticle with panitumumab under conditions to form the nanoparticle complex, such that the nanoparticle complex has EGFR binding specificity, and wherein the complex has a diameter of between 0.1 μm and 1 μm.

2. The antibody-albumin nanoparticle complex of claim 1 , said complex having a diameter of between 0.1 μm and 0.9 μm.

3. The antibody-albumin nanoparticle complex of claim 1 , said complex having a diameter of between 0.1 μm and 0.3 μm.

4. The antibody-albumin nanoparticle complex of claim 1 , wherein the ratio of albumin-paclitaxel nanoparticle to antibody is between 5:1 and 1:2.5.

5. The antibody-albumin nanoparticle complex of claim 1 , wherein said nanoparticle complex comprises an alkylating agent.

6. The antibody-albumin nanoparticle complex of claim 5 , wherein said alkylating agent is a platinum compound.

7. The antibody-albumin nanoparticle complex of claim 5 , wherein said alkylating agent is carboplatin.

8. A method of making a panitumumab antibody-albumin nanoparticle complex, the method comprising mixing in vitro an aqueous albumin-paclitaxel nanoparticle with panitumumab under conditions to form the nanoparticle complex, wherein the complex has a diameter of between 0.1 μm and 1 μm.

9. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and antibody-albumin nanoparticle complexes, said nanoparticle complexes comprising albumin, a panitumumab antibody, and paclitaxel, wherein the nanoparticle complexes have been pre-formed in vitro by mixing aqueous albumin-paclitaxel nanoparticles with the antibody under conditions to form the nanoparticle complexes, such that the nanoparticle complexes have EGFR binding specificity, and wherein the average diameter of said complexes is between 0.1 μm and 1 μm.

10. The pharmaceutical composition of claim 9 , wherein the average diameter of said complexes is between 0.1 μm and 0.9 μm.

11. The pharmaceutical composition of claim 9 , wherein the average diameter of said complexes is between 0.1 μm and 0.3 μm.

12. The pharmaceutical composition of claim 9 , wherein the ratio of albumin-paclitaxel nanoparticle to antibody is between 5:1 and 1:2.5.

13. The pharmaceutical composition of claim 9 which is formulated for injection.

14. The pharmaceutical composition of claim 9 , wherein the pharmaceutically acceptable carrier is saline, water, lactic acid, mannitol, or a combination thereof.

15. The pharmaceutical composition of claim 9 , wherein said composition comprises an alkylating agent.

16. The pharmaceutical composition of claim 15 , wherein said alkylating agent is a platinum compound.

17. The pharmaceutical composition of claim 15 , wherein said alkylating agent is carboplatin.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2016
From: MARKOVIC, SVETOMIR N.; NEVALA, WENDY K.
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 038985/0282 →
Continuity (4)
Continuation 14432979
Provisional Application 61708575 · Oct 1, 2012
Provisional Application 61725293 · Nov 12, 2012
Related Publication 20160324964A1 · Nov 10, 2016
Cited By (2)
US 12,364,754 US 12,403,119