IP Library Granted Patent US 7,812,001
Granted Patent B2
US 7,812,001 · App. 11/925,641 · Granted Oct 12, 2010

RNA aptamers and methods for identifying the same

Assignee: Duke University
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Quick Facts
Patent No.
US 7,812,001
App. No.
11/925,641
Granted
Oct 12, 2010
Kind
B2
Abstract

RNA aptamers and methods for identifying the same are disclosed. The RNA aptamers selectively bind coagulation factors, E2F family members, Ang1 or Ang2, and therapeutic and other uses for the RNA aptamers are also disclosed.

Claims (18)

1. A method of modulating the biological activity of a coagulation pathway factor VII or VIIa comprising administering to a host an effective amount of a RNA aptamer that binds to the coagulation factor VII or VIIa, wherein the aptamer comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs:39-47 and 74-101 and truncates thereof.

2. The method of claim 1 , wherein the aptamer comprises at least one 2′-modified nucleotide.

3. The method of claim 2 , wherein the aptamer comprises at least one modified nucleotide selected from the group consisting of a 2′-halo-modified nucleotide, a 2′-amino-modified and a 2′-O-alkyl-modified nucleotide.

4. The method of claim 2 , wherein the aptamer comprises at least one 2′-fluorocytidine or at least one 2′-fluorouridine.

5. The method of claim 2 , wherein the aptamer comprises cytidines that are all 2′-deoxy-2′-fluorocytidine, or uridines that are all 2′-deoxy-2′-fluorouridine.

6. The method of claim 2 , wherein the aptamer comprises at least one 2′-O-alkyl-modified nucleotide.

7. The method of claim 2 , wherein the aptamer comprises at least one 2′-amino-modified nucleotide.

8. The method of claim 2 , wherein the aptamer comprises cytidines that are all 2′-deoxy-2′-aminocytidine, or uridines that are all 2′-deoxy-2′-aminouridine.

9. The method of claim 1 , wherein the aptamer further comprises a covalently linked carrier selected from the group consisting of a soluble polymer, a biodegradable polymer, polyethylene glycol, and cholesterol.

10. The method of claim 1 , wherein the aptamer is administered orally, topically to a vascular tissue, intravenously, intraperitoneally, intramuscularly, subcutaneously, intra-cavity, transdermally, or by peristaltic techniques.

11. The method of claim 10 , wherein topical administration comprises coating or impregnating a blood vessel tissue with a gel comprising the aptamer and implanting the coated or impregnated vessel in place of a damaged or diseased vessel tissue segment in the host.

12. The method of claim 10 , wherein topical administration comprises delivery via a catheter to a vessel or vessels in the host.

13. The method of claim 10 , wherein topical administration comprises pumping an aptamer composition of the present invention into a vessel that is to be implanted into the host.

14. The method of claim 1 , wherein the aptamer is administered by injection of a unit dose.

15. The method of claim 1 , wherein the aptamer is administered at a dosage from about 1 μg/kg body weight to about 1 mg/kg body weight.

16. The method of claim 1 , wherein the aptamer comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 39-47 and 74-101.

17. The method of claim 1 , wherein the aptamer comprises the nucleotide sequence of SEQ ID NO: 75, or a truncate thereof.

18. The method of claim 1 , wherein the aptamer comprises the nucleotide sequence of SEQ ID NO: 88, or a truncate thereof.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded May 14, 2013
From: MIDCAP FINANCIAL SBIC, LP
To: REGADO BIOSCIENCES, INC.
Reel/Frame 030446/0312 →
SECURITY AGREEMENT Recorded May 27, 2011
From: REGADO BIOSCIENCES, INC.
To: MIDCAP FINANCIAL SBIC, LP
Reel/Frame 026357/0267 →
NUNC PRO TUNC ASSIGNMENT Recorded Dec 10, 2008
From: SULLENGER, BRUCE A.; RUSCONI, CHRISTOPHER P.; KONTOS, CHRISTOPHER D.; WHITE, REBEKAH R.
To: DUKE UNIVERSITY
Reel/Frame 021951/0428 →
Continuity (3)
Division 0996382700 · Sep 26, 2001
Provisional Application 6023565400 · Sep 26, 2000
Related Publication 20080182809A1 · Jul 31, 2008