IP Library Granted Patent US 8,367,629
Granted Patent B2
US 8,367,629 · App. 12/325,180 · Granted Feb 5, 2013

MCP-1 binding nucleic acids and use thereof

Inventors: Werner Purschke (Berlin, DE); Florian Jarosch (Berlin, DE); Dirk Eulberg (Berlin, DE); Sven Klussmann (Berlin, DE); Klaus Buchner (Berlin, DE); Christian Maasch (Berlin, DE)
Assignee: NOXXON Pharma AG
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Quick Facts
Patent No.
US 8,367,629
App. No.
12/325,180
Granted
Feb 5, 2013
Kind
B2
Abstract

The present invention is related to a nucleic acid molecule capable of binding to MCP-1, whereby the nucleic acid molecule is for use as a medicament for the treatment and/or prevention of a chronic disease or chronic disorder, preferably selected from the group consisting of chronic respiratory disease, chronic kidney disease and systemic lupus erythematosus.

Claims (14)

1. A treatment composition comprising two active agents consisting of (1) an L nucleic acid comprising SEQ ID NO:37 or a homolog thereof with at least 85% homology thereto and (2) a cyclophosphamide.

2. The composition of claim 1 , wherein SEQ ID NO:37 or homolog thereof binds monkey MCP-1, horse MCP-1, rabbit MCP-1, bovine MCP-1, canine MCP-1, porcine MCP-1 or human MCP-1.

3. The composition according to claim 1 , wherein SEQ ID NO:37 or homoloq thereof binds a human MCP-1.

4. The composition according to claim 1 , wherein SEQ ID NO:37 or homolog thereof binds the amino acid sequence according to SEQ ID NO:1.

5. The composition according to claim 1 , wherein SEQ ID NO:37 or homolog thereof comprises a modification.

6. The composition according to claim 5 , wherein the modification is selected from the group consisting of a HES moiety, a PEG moiety, a biodegradable modification and combinations thereof.

7. The composition according to claim 6 , wherein the PEG moiety comprises a straight or branched PEG.

8. The composition according to claim 6 , wherein the modification is a HES moiety.

9. The composition according to claim of 5 , wherein the modification is coupled to SEQ ID NO:37 or homolog thereof via a linker.

10. The composition of claim 6 , wherein said PEG moiety is at the 5′ terminus of SEQ ID NO:37 or homolog thereof.

11. The composition of claim 6 , wherein said PEG moiety is at the 3′ terminus of SEQ ID NO:37 or homolog thereof.

12. The composition of claim 6 , wherein said PEG moiety is from about 2 kD to about 200 kD.

13. The composition of claim 6 , wherein said PEG moiety is from about 40 kD to about 120 kD.

14. The composition of claim 1 , wherein said active agents are contained in a single vessel.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Feb 7, 2020
From: KREOS CAPITAL IV (UK) LIMITED
To: NOXXON PHARMA AG
Reel/Frame 051757/0649 →
SECURITY INTEREST Recorded Apr 27, 2015
From: NOXXON PHARMA AG
To: KREOS CAPITAL IV (UK) LIMITED
Reel/Frame 035501/0893 →
SECURITY INTEREST Recorded Mar 13, 2014
From: NOXXON PHARMA AG
To: KREOS CAPITAL IV (UK) LIMITED
Reel/Frame 032422/0064 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2009
From: PURSCHKE, WERNER; JAROSCH, FLORIAN; EULBERG, DIRK; KLUSSMANN, SVEN; BUCHNER, KLAUS; MAASCH, CHRISTIAN
To: NOXXON PHARMA AG
Reel/Frame 022185/0085 →
Priority Claims (3)
EP 06002935 · Feb 14, 2006 · regional
EP 06024202 · Nov 22, 2006 · regional
EP 07023267 · Nov 30, 2007 · regional
Continuity (2)
Continuation In Part 12279183
Related Publication 20090156542A1 · Jun 18, 2009