IP Library › Granted Patent US 12,133,844
Granted Patent B2
US 12,133,844 · App. 17/165,652 · Granted Nov 5, 2024

Methods of treating epithelioid cell tumors

Inventor: Neil P. Desai (Pacific Palisades, CA)
Assignee: Abraxis BioScience, LLC
A61K31/436A61K9/0019A61K9/08A61K9/10A61K9/19A61K9/5169A61K38/38A61K47/42A61P35/00A61P35/04
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Quick Facts
Patent No.
US 12,133,844
App. No.
17/165,652
Granted
Nov 5, 2024
Kind
B2
Abstract

The present invention provides methods and compositions for treating epithelioid cell tumors (such as a PEComa) by administering a composition comprising nanoparticles comprising an mTOR inhibitor and an albumin.

Claims (14)

1. A method of treating a malignant perivascular epithelioid tumor (PEComa) in an individual, comprising intravenously administering to the individual an effective amount of a composition comprising nanoparticles comprising sirolimus and an albumin, wherein the effective amount of sirolimus in the nanoparticle composition is about 10 mg/m 2 to about 100 mg/m 2 , and wherein the nanoparticle composition is administered on days 1 and 8 of a 21-day cycle.

2. The method of claim 1 , wherein the malignant PEComa is a pulmonary clear cell ‘sugar’ tumor or a PEComa not otherwise specified (PEComa-NOS).

3. The method of claim 1 , wherein the malignant PEComa is advanced malignant, locally advanced, metastatic, or recurrent.

4. The method of claim 1 , wherein the individual has been previously treated with an mTOR inhibitor.

5. The method of claim 1 , wherein the effective amount of sirolimus in the nanoparticle composition is less than about 50 mg/m 2 .

6. The method of claim 1 , wherein the effective amount of sirolimus in the nanoparticle composition is about 10 mg/m 2 to about 25 mg/m 2 .

7. The method of claim 1 , wherein the effective amount of sirolimus in the nanoparticle composition is about 25 mg/m 2 to about 50 mg/m 2 .

8. The method of claim 1 , wherein the effective amount of sirolimus in the nanoparticle composition is about 10 mg/m 2 to about 56 mg/m 2 .

9. The method of claim 1 , wherein the effective amount of sirolimus in the nanoparticle composition is about 45 mg/m 2 , about 30 mg/m 2 , or about 10 mg/m 2 .

10. The method of claim 1 , wherein the method is in a neoadjuvant setting.

11. The method of claim 1 , wherein the nanoparticles in the composition have an average diameter of no greater than about 150 nm.

12. The method of claim 1 , wherein the albumin is human albumin.

13. The method of claim 1 , wherein the albumin is human serum albumin.

14. The method of claim 1 , wherein the individual is human.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2021
From: DESAI, NEIL P.
To: ABRAXIS BIOSCIENCE, LLC
Reel/Frame 055322/0428 →
Continuity (3)
Continuation 15737936
Provisional Application 62186252 · Jun 29, 2015
Related Publication 20210322391A1 · Oct 21, 2021