IP Library › Granted Patent US 10,233,242
Granted Patent B2
US 10,233,242 · App. 14/576,990 · Granted Mar 19, 2019

CTLA4 fusion proteins for the treatment of diabetes

Inventor: Tihamer Orban (Brookline, MA)
Assignee: DMNOMORE
C07K16/2827A61K38/1774C07K14/70521C07K16/2818A61K9/0019A61K2039/505C07K2317/76C07K2319/30C07K2319/32
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Quick Facts
Patent No.
US 10,233,242
App. No.
14/576,990
Granted
Mar 19, 2019
Kind
B2
Abstract

A method of treating, preventing, or delaying the progression of Type 1 diabetes mellitus autoimmunity by administering an effective amount of a cytotoxic T-lymphocyte-associated antigen 4 (CTLA4) molecule is provided herewith. The CTLA4 molecule may be a fusion protein of a CTLA4 extracellular region and an immunoglobulin, such as abatacept.

Claims (13)

1. A method of treating type 1 diabetes mellitus in a subject comprising administering an effective amount of a fusion protein composition which comprises a fusion protein and an oil-based carrier, wherein the fusion protein comprises the extracellular domain of CTLA4 and a portion of an immunoglobulin molecule, and wherein the oil-based carrier is a water-in-oil emulsion.

2. The method of claim 1 wherein the composition comprises Abatacept.

3. The method of claim 1 wherein the composition is administered as a pharmaceutically acceptable salt.

4. The method of claim 1 , wherein the composition is administered by intravenous infusion.

5. The method of claim 4 , wherein the composition is administered by intravenous infusion in about 50 to 200 ml of physiological saline.

6. The method of claim 4 , wherein the composition is administered at a dose ranging from about 5 mg/kg to about 50 mg/kg.

7. The method of claim 4 , wherein the intravenous infusion of the composition is repeated over time.

8. The method of claim 4 , wherein the intravenous infusion of the composition is repeated at least once following a time interval ranging from about one week to about two months.

9. The method of claim 4 , wherein the composition is administered at a dose ranging from about 250 to 2000 mg.

10. The method of claim 9 , wherein the composition is administered at a dose of 500 mg.

11. The method of claim 9 , wherein the composition is administered at a dose of 750 mg.

12. The method of claim 9 , wherein the composition is administered at a dose of 1000 mg.

13. The method of claim 1 , wherein the subject is white.

Assignments (3)
CHANGE OF NAME Recorded Aug 11, 2022
From: DMNOMORE LIMITED
To: PHAIM PHARMA LTD
Reel/Frame 060781/0365 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2015
From: ORBAN BIOTECH LLC
To: DMNOMORE
Reel/Frame 036880/0640 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 19, 2015
From: ORBAN, TIHAMER
To: ORBAN BIOTECH LLC
Reel/Frame 036362/0821 →
Continuity (3)
Continuation 14021629 · Sep 9, 2013
Continuation 13534560 · Jun 27, 2012
Related Publication 20150104451A1 · Apr 16, 2015