IP Library Granted Patent US 8,586,032
Granted Patent B2
US 8,586,032 · App. 12/449,192 · Granted Nov 19, 2013

Use of alkaline phosphatase in the treatment of reduced renal function

Inventors: Roelof P. Pickkers (Nijmegen, NL); Suzanne Heemskerk (Nijmegen, NL); Markwin P. Velders (Bilthoven, NL); Willem Raaben (Amersfoort, NL); Marty B. F. Wulferink (Ede, NL)
Assignee: AM-Pharma B.V.
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Quick Facts
Patent No.
US 8,586,032
App. No.
12/449,192
Granted
Nov 19, 2013
Kind
B2
Abstract

The invention relates to the field of medicine and in particular to the use of alkaline phosphatase in the treatment of renal diseases, such as reduced renal function. The present invention also relates to the field of pharmacy and in particular to the pharmaceutical use of alkaline phosphatase. The present invention provides an alternative treatment to improve a situation in which the renal function is reduced by using alkaline phosphatase.

Claims (11)

1. A method for treating a subject with reduced renal function due to renal failure, the method comprising: administering intravenously an effective amount of mammalian alkaline phosphatase (“AP”) to a subject with reduced renal function due to renal failure.

2. The method according to claim 1 , wherein the reduced renal function is induced or sustained or exacerbated due to acute renal failure.

3. The method according to claim 1 , wherein the reduced renal function is induced or sustained or exacerbated by intrinsic acute renal failure.

4. The method according to claim 3 , wherein the intrinsic acute renal failure is acute tubular cellular damage.

5. The method according to claim 3 , wherein the intrinsic acute renal failure is glomerulonephritis.

6. The method according to claim 1 , wherein the AP is human AP.

7. The method according to claim 1 , wherein the AP is placental AP, placental-like AP, intestinal AP, or liver/bone/kidney AP.

8. The method according to claim 1 , wherein the AP is recombinant.

9. The method according to claim 1 , wherein the renal failure is chronic renal failure.

10. The method according to claim 1 , wherein the renal failure is acute renal failure.

11. The method according to claim 1 , wherein prior to said administration the subject has a baseline serum creatinine level of greater than 150 μmol/L or is already on renal replacement therapy.

Assignments (5)
RECORDATION OF ADDRESS CHANGE Recorded Jul 2, 2020
From: AM PHARMA B.V.
To: AM PHARMA B.V.
Reel/Frame 053122/0180 →
SECURITY INTEREST Recorded Feb 24, 2020
From: AM-PHARMA B.V.
To: EUROPEAN INVESTMENT BANK
Reel/Frame 052004/0398 →
PLEDGE CANCELLATION AGREEMENT Recorded Dec 19, 2012
From: AM-PHARMA B.V.; PHARMAAWARE IP B.V.; PHARMAAWARE SEPSIS B.V.
To: LV L.P.; COOPERATIEVE AAC LS U.A.
Reel/Frame 029505/0637 →
SECURITY AGREEMENT Recorded Mar 22, 2011
From: AM-PHARMA B.V.
To: LV L.P.; COOPERATIEVE AAC LS U.A.
Reel/Frame 026000/0273 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2010
From: PICKKERS, ROELOF P.; HEEMSKERK, SUZANNE; VELDERS, MARKWIN P.; RAABEN, WILLEM; WULFERINK, MARTY B. F.
To: AM-PHARMA B.V.
Reel/Frame 023770/0785 →
Priority Claims (1)
EP 07101437 · Jan 30, 2007 · regional
Continuity (1)
Related Publication 20100111923A1 · May 6, 2010