IP Library Granted Patent US 9,545,420
Granted Patent B2
US 9,545,420 · App. 14/417,763 · Granted Jan 17, 2017

Method of promoting wound healing

Inventor: Prabha Sampath (Singapore, SG)
Assignee: Agency for Science, Technology and Research
A61K31/7088A61K38/1709C12N15/1136C12N2310/113C12N2310/14C12N2310/315C12N2310/322C12N2310/3231C12N2320/31
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Quick Facts
Patent No.
US 9,545,420
App. No.
14/417,763
Granted
Jan 17, 2017
Kind
B2
Abstract

Disclosed is a method of promoting wound healing or wound closure. The method comprises administration of a miR-198 inhibitor and/or a follistatin-like-1 (FSTL1) polypeptide. Also disclosed are method of treating chronic cutaneous wounds, method of identifying a non-healing wound, use and a pharmaceutical composition comprising a miR-198 inhibitor and/or a follistatin-like-1 (FSTL1) polypeptide.

Claims (14)

1. A method of promoting wound healing or wound closure, wherein the method comprises administration of a miR-198 inhibitor and a follistatin-like-1 (FSTL1) polypeptide.

2. A method of treating chronic cutaneous wounds, wherein the method comprises administration of a miR-198 inhibitor and a follistatin-like-1 (FSTL1) polypeptide.

3. The method of claim 1 , further comprising administration of TGF-β1 either simultaneously or before or after administration of the miR-198 inhibitor and the FSTL1 polypeptide.

4. The method of claim 1 , wherein in case miR-198 inhibitor and follistatin-like-1 (FSTL1) polypeptide are administered simultaneously or separately from each other.

5. The method of claim 2 , wherein the chronic cutaneous wounds are the wounds of a patient suffering or suspected to be suffering from diabetes mellitus.

6. The method of claim 2 , wherein the chronic cutaneous wound is diabetic ulcer.

7. The method of claim 1 , wherein administration is via systemic or topical administration.

8. The method of claim 7 , wherein administration is via topical administration.

9. The method of claim 1 , wherein the miR-198 inhibitor and FSTL1 polypeptide are administered independently of each other in an amount of between about 10 μg to 300 mg/kg body weight.

10. The method of claim 1 , wherein TGF-β1 is administered in an amount of between about 10 μg to 300 mg/kg body weight.

11. The method of claim 1 , wherein the miR-198 inhibitor is selected from the group of an anti-miR-198, peptide nucleic acid (PNA) derivatives of miR-198 inhibitor sequence and Tiny LNA anti-miRs for seed-sequence of the inhibitor.

12. The method of claim 1 , wherein the miR-198 inhibitor has the sequence: 5′-GAACCUAUCUCCCCUCUGGACC-3′ (SEQ ID NO: 1).

13. The method of claim 12 , wherein the inhibitor is unmodified.

14. The method of claim 12 , wherein the inhibitor is with at least one modification/s selected from the group consisting of 1) full or partial 2′-O-methoxy ethyl modification, 2) full or partial phosphorothioate modification, 3) cholesterol modification of 3′ end of the miR-198 inhibitor and 4) full or partial locked nucleic acid modification (LNA) of nucleotides.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2015
From: SAMPATH, PRABHA
To: AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH
Reel/Frame 034896/0697 →
Priority Claims (1)
SG 201205614 · Jul 27, 2012 · national
Continuity (1)
Related Publication 20150290289A1 · Oct 15, 2015