IP Library Granted Patent US 7,291,604
Granted Patent B2
US 7,291,604 · App. 10/933,807 · Granted Nov 6, 2007

Methods of treating restenosis

Assignee: The General Hospital Corporation
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,291,604
App. No.
10/933,807
Granted
Nov 6, 2007
Kind
B2
Abstract

Restenosis in a subject can be treated by administering to a tissue, e.g., a blood vessel, of the subject an agent that increases SERCA activity. For example, a stent that is coated with the agent can be introduced into a blood vessel.

Claims (8)

1. A method of reducing restenosis in a subject following angioplasty, the method comprising directly administering to the injured blood vessel of said subject a nucleic acid that encodes a SERCA2a polypeptide, wherein the nucleic acid is a component of an adenovirus-based vector, thereby reducing restenosis.

2. The method of claim 1 , wherein the nucleic acid encodes SERCA2a operably linked to a viral promoter.

3. The method of claim 1 , wherein the nucleic acid encodes SERCA2a operably linked to an inducible promoter.

4. The method of claim 1 , wherein the nucleic acid is administered in an amount effective to reduce neointimal hyperplasia.

5. A method of reducing restenosis in a subject folloeing angioplasty, the method comprising directly administering to the injured blood vessel of said subject a nucleic acid that encodes a SERCA 2 a polypeptide, wherein the nucleic acid is a component of an adeno-associated virus-based vector, thereby reducing restenosis,

6. The method of claim 5 , wherein the nucleic acid encodes SERCA 2 a operably linked to a viral promoter.

7. The method of claim 5 , wherein the nucleic acid encodes SERCA 2 a operably linked to an inducible promoter.

8. The method of claim 5 , wherein the nucleic acid is administered in an amount effective to reduce neointimal hyperplasia.

Assignments (4)
CONFIRMATORY LICENSE Recorded Feb 4, 2019
From: THE GENERAL HOSPITAL CORPORATION
To: NIH - DEITR
Reel/Frame 048226/0379 →
CONFIRMATORY LICENSE Recorded Feb 23, 2010
From: GENERAL HOSPITAL CORPORATIOND DBA MASSACHUSETTS GENERAL HOSPITAL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023978/0129 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2006
From: HAJJAR, ROGER J.; MONTE, FEDERICA DEL
To: GENERAL HOSPITAL CORPORATION, THE
Reel/Frame 017640/0265 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2004
From: LOMPR, ANNE-MARIE; LIPSKAIA, LARISSA
To: INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)
Reel/Frame 015347/0457 →
Continuity (2)
Provisional Application 6049970500 · Sep 3, 2003
Related Publication 20050112101A1 · May 26, 2005