IP Library Granted Patent US 9,409,963
Granted Patent B2
US 9,409,963 · App. 13/322,124 · Granted Aug 9, 2016

Fibromodulin peptide

Inventors: B. Chia Soo (Beverly Hills, CA); Kang Ting (Beverly Hills, CA); Zhong Zheng (Van Nuys, CA)
Assignee: The Regents of the University of California
C07K14/4725A61K38/1841C07K2319/02C07K2319/21
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Quick Facts
Patent No.
US 9,409,963
App. No.
13/322,124
Granted
Aug 9, 2016
Kind
B2
Abstract

Embodiments of the present invention provide a fibromodulin (FMOD) peptide (FMOD-P), a composition and a formulation comprising a FMOD-P, option-ally with a TGF-β isoform, or comprising FMOD with a TGF-β isoform. The present invention also provides methods of making and using the FMOD-P, composition, or formulation.

Claims (13)

1. An isolated fibromodulin (FMOD) peptide (FMOD-P), wherein FMOD-P is a chemically modified isoform of a full length FMOD, wherein the FMOD-P consists of an amino acid sequence selected from the group consisting of SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO:24, SEQ ID NO: 26, SEQ ID NO: 28, and SEQ ID NO: 34, and wherein the chemically modified isoform is achieved by using an acid, a base, esterification, PEGylation, or alkylation with a short chain alkyl group.

2. The FMOD-P of claim 1 , wherein the isolated FMOD-P binds one TGF-β selected from the group consisting of TGF-β1, TGF-β2, and TGF-β3.

3. A composition, comprising a pharmaceutically acceptable carrier and an effective amount of any of the following ingredients:

a) an isolated FMOD-P;

b) a combination of two or more isolated FMOD-P;

c) an isolated FMOD-P or a combination of two or more isolated FMOD-P and at least one TGF-β isoform;

d) isolated FMOD and isolated FMOD-P or a combination of two or more isolated FMOD-P; and

e) any combination of (a)-(d), wherein FMOD-P is an isoform of a full length FMOD, wherein the at least one TGF-β isoform is selected from the group consisting of TGF-β1, TGF-β2, TGF-β3, and a combination thereof, wherein the isolated FMOD-P consists of an amino acid sequence selected from the group consisting of SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, and SEQ ID NO: 34, and wherein FMOD consists of an amino acid sequence selected from the group consisting of SEQ ID NO. 1, SEQ ID NO. 2, SEQ ID NO. 3, SEQ ID NO. 4, SEQ ID NO. 5, SEQ ID NO. 6, SEQ ID NO. 7, SEQ ID NO. 8, SEQ ID NO. 9, SEQ ID NO. 10, SEQ ID NO. 11, and SEQ ID NO. 12.

4. The composition of claim 3 , wherein the isolated FMOD-P binds one TGF-β selected from the group consisting of TGF-β1, TGF-β2, and TGF-β3.

5. The composition of claim 3 , further comprising an excipient.

6. The composition of claim 5 , wherein the excipient is a pharmaceutically acceptable carrier or dermatologically acceptable carrier.

7. A formulation comprising the composition of claim 3 and an excipient, wherein the formulation is for systemic or local delivery.

8. The formulation of claim 7 , wherein the local delivery is topical delivery, transdermal delivery, intradermal delivery, micro needle delivery, delivery as a coating on medical devices, or delivery by impregnating or coating on scaffold devices, and wherein the systemic delivery is injection, oral administration, nasal delivery, or inhalation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 16, 2012
From: SOO, B. CHIA; TING, KANG; ZHENG, ZHONG
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 029316/0302 →
Continuity (2)
Provisional Application 61181226 · May 26, 2009
Related Publication 20120171253A1 · Jul 5, 2012