IP Library › Granted Patent US 10,213,513
Granted Patent B2
US 10,213,513 · App. 15/030,568 · Granted Feb 26, 2019

Treating myelomas

Inventors: Svetomir N. Markovic (Rochester, MN); Wendy K. Nevala (Rochester, MN)
Assignee: Mayo Foundation for Medical Education and Research
A61K47/48561A61K9/0019A61K9/5169A61K31/337A61K47/643A61K47/6849
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Quick Facts
Patent No.
US 10,213,513
App. No.
15/030,568
Granted
Feb 26, 2019
Kind
B2
Abstract

This document provides methods and materials related to treating myelomas. For example, methods and materials relating to the use of a composition containing albumin-containing nanoparticle/antibody complexes (e.g., ABRAXANE®/anti-CD38 polypeptide antibody complexes) to treat myelomas are provided.

Claims (12)

1. A method for treating a mammal having myeloma, said method comprising administering to said mammal an effective amount of a composition comprising nanoparticles containing albumin-bound paclitaxel complexed with an anti-CD38 polypeptide antibody, said complexed nanoparticles having an average diameter of less than 1 μm, wherein the effective amount is an amount that treats the myeloma,

wherein the effective amount for the anti-CD38 polypeptide antibody is about 5 mg/kg to about 20 mg/kg.

2. The method of claim 1 , wherein the anti-CD38 antibody is daratumumab, MOR202 or SAR650984.

3. The method of claim 1 , wherein the composition is administered by injection.

4. The method of claim 1 , wherein the average diameter of the complexed nanoparticles is from about 0.1 μm to about 0.3 μm.

5. The method of claim 1 , wherein the effective amount is between about 50 mg/m 2 to about 150 mg/m 2 of albumin and paclitaxel.

6. The method of claim 1 , wherein the mammal is a human.

7. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable excipient.

8. The method of claim 7 , wherein the pharmaceutically acceptable excipient comprises saline, water, lactic acid, mannitol, or a combination thereof.

9. The method of claim 1 , wherein the treatment increases the length of progression-free survival in the mammal.

10. The method of claim 1 , wherein the amount of the anti-CD38 polypeptide antibody in the composition is about 2 mg/mL.

11. The method of claim 1 , wherein the concentration ratio of the nanoparticles to the anti-CD38 polypeptide antibody is 5:2.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2016
From: MARKOVIC, SVETOMIR N.; NEVALA, WENDY K.
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 038710/0798 →
Continuity (2)
Provisional Application 62012804 · Jun 16, 2014
Related Publication 20160263241A1 · Sep 15, 2016