IP Library Granted Patent US 11,965,160
Granted Patent B2
US 11,965,160 · App. 17/146,147 · Granted Apr 23, 2024

Von Willebrand Factor (VWF)-targeting agents and methods of using the same

Inventors: Shahid M. Nimjee (Columbus, OH); Bruce Sullenger (Durham, NC); George A. Pitoc (Durham, NC); Juliana Layzer (Durham, NC)
Assignees: Duke University; Ohio State Innovation Foundation
C12N15/113A61K31/7088A61K31/7105A61K31/7115A61K45/06A61K47/554A61K47/60A61K47/64A61P7/02C12N15/115C12N2310/113C12N2310/16C12N2310/317C12N2310/3183C12N2310/3515
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Quick Facts
Patent No.
US 11,965,160
App. No.
17/146,147
Granted
Apr 23, 2024
Kind
B2
Abstract

Provided herein are aptamers capable of inhibiting the activity of Von Willebrand Factor (VWF). Pharmaceutical compositions comprising these aptamers are also provided. Methods of preventing blood clot formation in a subject by administering the aptamers are provided and methods of treating a blood clot by administering a VWF-targeting agent are also provided.

Claims (20)

1. An antidote comprising a polynucleotide having at least 90% sequence identity to SEQ ID NO: 157, wherein the antidote is no more than 24 nucleotides in length.

2. An antidote comprising a polynucleotide having sequence reverse complementary to and capable of hybridizing to at least 8 nucleotides of an aptamer comprising a polynucleotide of SEQ ID NO: 3, or a polynucleotide with at least 90% sequence identity to SEQ ID NO: 3 and wherein the antidote is no more than 24 nucleotides in length.

3. A pharmaceutical composition comprising a pharmaceutical carrier and any one of the antidotes of claim 1 .

4. A method for preventing blood clot formation in a subject comprising administering to the subject a composition comprising a polynucleotide of SEQ ID NOs: 3, or a polynucleotide with at least 90% sequence identity to SEQ ID NO: 3, in a therapeutically effective amount to prevent blood clot formation in the subject and further administering to the subject an antidote of claim 1 in a therapeutically effective amount to neutralize the composition.

5. The method of claim 4 , wherein the subject suffers from atrial fibrillation or is at risk of having a Deep Vein Thrombosis, a stroke, a heart attack, or a pulmonary embolism.

6. The method of claim 4 , wherein the subject is a mammal.

7. The method of claim 6 , wherein the mammal is a human.

8. A pharmaceutical composition comprising a pharmaceutical carrier and any one of the antidotes of claim 2 .

9. A method for preventing blood clot formation in a subject comprising administering to the subject a composition comprising a polynucleotide of SEQ ID NOs: 3, or a polynucleotide with at least 90% sequence identity to SEQ ID NO: 3 in a therapeutically effective amount to prevent blood clot formation in the subject and further administering to the subject an antidote of claim 2 in a therapeutically effective amount to neutralize the composition.

10. The method of claim 9 , wherein the subject suffers from atrial fibrillation or is at risk of having a Deep Vein Thrombosis, a stroke, a heart attack, or a pulmonary embolism.

11. The method of claim 9 , wherein the subject is a mammal.

12. The method of claim 11 , wherein the mammal is a human.

13. A method of neutralizing an aptamer in a subject, the method comprising administering an antidote of claim 1 to a subject who has received a composition comprising an aptamer comprising a polynucleotide of SEQ ID NOs: 3, or a polynucleotide with at least 90% sequence identity to SEQ ID NO: 3 wherein the antidote is administered in a therapeutically effective amount to neutralize the composition.

14. The method of claim 13 , wherein the subject suffers from atrial fibrillation or is at risk of having a Deep Vein Thrombosis, a stroke, a heart attack, or a pulmonary embolism.

15. A method of neutralizing an aptamer in a subject, the method comprising administering an antidote of claim 2 to a subject who has received a composition comprising an aptamer comprising a polynucleotide of SEQ ID NOs: 3, or a polynucleotide with at least 90% sequence identity to SEQ ID NO: 3 wherein the antidote is administered in a therapeutically effective amount to neutralize the composition.

16. The method of claim 15 , wherein the subject suffers from atrial fibrillation or is at risk of having a Deep Vein Thrombosis, a stroke, a heart attack, or a pulmonary embolism.

17. The method of claim 15 , wherein the subject is a mammal.

18. The method of claim 17 , wherein the mammal is a human.

19. An antidote comprising a polynucleotide capable of hybridizing to 8 to 24 nucleotides of an aptamer of SEQ ID NO: 3 and having at least 80% sequence identity to SEQ ID NO: 157 and wherein the antidote is no more than 24 nucleotides in length.

20. A method of neutralizing an aptamer in a subject, the method comprising administering the antidote of claim 19 to a subject who has received a composition comprising an aptamer, wherein the aptamer is a polynucleotide of SEQ ID NO:3, or a polynucleotide with at least 90% sequence identity to SEQ ID NO: 3, and wherein the antidote is administered in a therapeutically effective amount to neutralize the composition.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2021
From: SULLENGER, BRUCE; PITOC, GEORGE A.; LAYZER, JULIANA
To: DUKE UNIVERSITY
Reel/Frame 055395/0222 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2021
From: NIMJEE, SHAHID M.
To: OHIO STATE INNOVATION FOUNDATION
Reel/Frame 055405/0406 →
Continuity (3)
Division 16334307
Provisional Application 62395642 · Sep 16, 2016
Related Publication 20210222170A1 · Jul 22, 2021