IP Library Granted Patent US 7,560,487
Granted Patent B2
US 7,560,487 · App. 10/250,465 · Granted Jul 14, 2009

Use of (R)—ibuprofen methanesulfonamide and salts thereof in the treatment and prevention of rejection reactions of transplanted organs

Assignee: Dompé Pha.r.ma S.p.A.
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 7,560,487
App. No.
10/250,465
Granted
Jul 14, 2009
Kind
B2
Abstract

The use of (R)-ibuprofen methanesulfonamide is described for the preparation of medicaments for the treatment and prevention of functional injury resulting from rejection reactions of transplanted organs. In particular, the use of non-toxic salts of (R)-ibuprofen methanesulfonamide, such as the (L)-lysine salt, is described for the prevention and the treatment of rejection reactions of transplanted kidneys.

Claims (7)

1. A method of preserving renal function in connection with a syngeneic kidney transplant in a patient, comprising administering to said patient prior to, during and/or after said transplant in said patient (R)-ibuprofen methanesulfonamide, or a non-toxic salt thereof in an amount effective to preserve renal function.

2. The method according to claim 1 , wherein the non-toxic salt is the L-lysine or DL-lysine salt.

3. The method according to claim 2 , wherein the non-toxic salt is the L-lysine salt.

4. The method of claim 1 , wherein said (R)-ibuprofen methanesulfonamide or a non-toxic salt thereof is administered in oral, parenteral, rectal or topical routes, before and/or after transplantation surgery.

5. The method of claim 4 , wherein said (R)-ibuprofen methanesulfonamide or a non-toxic salt thereof is in the form of a capsule, tablet, suppository, syrup, drop, suspension, emulsion, injectable sterile solution, sterile lyophilized powder for injection, controlled release formulation, transdermal formulation or ointment.

6. The method of claim 4 , wherein said (R)-ibuprofen methanesulfonamide or a non-toxic salt thereof is administered in a dosage of 1 to 500 mg.

7. The method of claim 4 , wherein said (R)-ibuprofen methanesulfonamide or a non-toxic salt thereof is administered in a single or multiple dose.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY'S ADDRESS PREVIOUSLY RECORDED AT REEL: 036914 FRAME: 0863. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER. Recorded Oct 6, 2016
From: DOMPÉ S.P.A.
To: DOMPÉ FARMACEUTICI S.P.A.
Reel/Frame 040246/0700 →
MERGER Recorded Oct 29, 2015
From: DOMPE' PHA.R.MA S.P.A.
To: DOMPÉ S.P.A.
Reel/Frame 036914/0385 →
MERGER Recorded Oct 29, 2015
From: DOMPÉ S.P.A.
To: DOMPÉ FARMACEUTICI S.P.A.
Reel/Frame 036914/0863 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 21, 2007
From: DOMPE S.P.A.
To: DOMPE PHA.R.MA S.P.A.
Reel/Frame 019864/0480 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 2, 2003
From: BERTINI, RICCARDO; COLOTTA, FRANCESCO; NOVELLINI, ROBERTO
To: DOMPE' S.A.
Reel/Frame 014547/0252 →
Priority Claims (1)
IT MI2001A0206 · Feb 2, 2001 · national
Continuity (1)
Related Publication 20040102520A1 · May 27, 2004