IP Library Granted Patent US 8,697,657
Granted Patent B2
US 8,697,657 · App. 13/634,192 · Granted Apr 15, 2014

Combination therapies using cyclosporine and aromatic cationic peptides

Inventor: D. Travis Wilson (Newton, MA)
Assignee: Stealth Peptides International, Inc.
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Quick Facts
Patent No.
US 8,697,657
App. No.
13/634,192
Granted
Apr 15, 2014
Kind
B2
Abstract

The invention provides compositions and methods for preventing or treating an ischemia-reperfusion injury, such as occurs during acute myocardial infarction and organ transplant in a mammalian subject. The methods comprise administering to the subject an effective amount of an aromatic-cationic peptide or a pharmaceutically acceptable salt thereof, and one or more additional active agents such as cyclosporine.

Claims (13)

1. A method for treating ischemia and/or reperfusion injury in a subject in need thereof, the method comprising administering an effective amount of (i) an aromatic-cationic peptide or a pharmaceutically acceptable salt thereof, wherein the aromatic-cationic peptide is selected from the group consisting of: Tyr-D-Arg-Phe-Lys-NH 2 ; 2′,6′-Dmt-D-Arg-Phe-Lys-NH 2 ; Phe-D-Arg-Phe-Lys-NH 2 ; 2′,6′-Dmp-D-Arg-Phe-Lys-NH 2 ; and D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 and (ii) an additional active agent consisting of cyclosporine; wherein the aromatic-cationic peptide is linked to cyclosporine by a linker.

2. The method of claim 1 , wherein the pharmaceutically acceptable salt comprises acetate salt or trifluororacetate salt.

3. The method of claim 1 , wherein the additional active agent comprises cyclosporine A.

4. The method of claim 1 , wherein the aromatic-cationic peptide comprises D-Arg-2′6′-Dmt-Lys-Phe-NH 2 or a pharmaceutically acceptable salt thereof selected from acetate salt or trifluororacetate salt, and wherein the additional active agent is cyclosporine A.

5. A composition comprising: an (i) an aromatic-cationic peptide or a pharmaceutically acceptable salt thereof, wherein the aromatic-cationic peptide is selected from the group consisting of: Tyr-D-Arg-Phe-Lys-NH 2 ; 2′,6′-Dmt-D-Arg-Phe-Lys-NH 2 ; Phe-D-Arg-Phe-Lys-NH 2 ; 2′,6′-Dmp-D-Arg-Phe-Lys-NH 2 ; and D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 , and (ii) an additional active agent consisting of cyclosporine; wherein the aromatic-cationic peptide is linked to cyclosporine by a linker.

6. The composition of claim 5 , wherein the pharmaceutically acceptable salt comprises acetate salt or trifluororacetate salt.

7. The composition of claim 5 , wherein the additional active agent comprises cyclosporine A.

8. The composition of claim 5 , wherein the aromatic-cationic peptide comprises D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 or a pharmaceutically acceptable salt thereof selected from acetate salt or trifluororacetate salt; wherein the additional active agent is cyclosporine A; and wherein the linker comprises an enzyme-cleavable linker.

9. The method of claim 1 , wherein the aromatic-cationic peptide is administered intravenously, intradermally, intraperitoneally, subcutaneously, orally, transdermally, topically, intraocularly, iontophoretically, transmucosally, or by inhalation.

10. The method of claim 1 , wherein the ischemia and/or reperfusion injury comprises vessel occlusion injury or cardiac ischemia-reperfusion injury.

11. The composition of claim 5 , wherein the aromatic-cationic peptide is administered intravenously, intradermally, intraperitoneally, subcutaneously, orally, transdermally, topically, intraocularly, iontophoretically, transmucosally, or by inhalation.

12. The composition of claim 5 , wherein the aromatic-cationic peptide comprises D-Arg-2′,6′-Dmt-Lys-Phe-NH2 or a pharmaceutically acceptable salt thereof selected from acetate salt or trifluororacetate salt; wherein the additional active agent is cyclosporine A; and wherein the linker comprises a pH-sensitive linker.

13. The method of claim 4 , wherein the linker is selected from the group consisting of an enzyme-cleavable linker and a pH-sensitive linker.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2021
From: STEALTH BIOTHERAPEUTICS CORP
To: STEALTH BIOTHERAPEUTICS INC.
Reel/Frame 058164/0305 →
CHANGE OF NAME Recorded Mar 24, 2017
From: STEALTH PEPTIDES INTERNATIONAL, INC.
To: STEALTH BIOTHERAPEUTICS CORP
Reel/Frame 042085/0568 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2017
From: WILSON, D. TRAVIS
To: STEALTH PEPTIDES INTERNATIONAL, INC.
Reel/Frame 041609/0592 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2012
From: WILSON, D. TRAVIS; WILSON, D. TRAVIS
To: STEALTH PEPTIDES INTERNATIONAL, INC.
Reel/Frame 029494/0579 →
Continuity (3)
Provisional Application 61313945 · Mar 15, 2010
Provisional Application 61376813 · Aug 25, 2010
Related Publication 20130059784A1 · Mar 7, 2013