IP Library Granted Patent US 10,519,213
Granted Patent B2
US 10,519,213 · App. 16/517,988 · Granted Dec 31, 2019

Fusion proteins of collagen-binding domain and parathyroid hormone

Inventors: Robert C. Gensure (Lexington, MA); Joshua Sakon (Fayetteville, AR); Osamu Matsushita (Okayama, JP); Tulasi Ponnapakkam (Metairie, LA)
Assignees: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS; OCHSNER CLINIC FOUNDATION; NATIONAL UNIVERSITY CORPORATION KAGAWA UNIVERSITY
C07K14/635A61K8/64A61K8/66A61K9/0019A61K35/28A61K38/164A61K38/29A61K38/4886A61Q7/00C12N9/1088C12N9/50C12N9/52C12N9/6489C12Y205/01018C12Y304/24003C12Y304/24007A61K2800/86A61K2800/91C07K2319/00C07K2319/50C07K2319/70
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Quick Facts
Patent No.
US 10,519,213
App. No.
16/517,988
Granted
Dec 31, 2019
Kind
B2
Abstract

Fusion proteins containing active agonist or antagonist fragments of parathyroid hormone (PTH) and parathyroid hormone related peptide (PTHrP) coupled to a collagen-binding domain are presented. The fusion proteins can be used to promote bone growth, to promote hair growth, to prevent cancer metastasis to bone, to promote immune reconstitution with a bone marrow stem cell transplant, to promote mobilization of bone marrow stem cells for collection for autologous stem cell transplant, and to treat renal osteodystrophy. Pharmaceutical agents comprising a collagen-binding polypeptide segment linked to a non-peptidyl PTH/PTHrP receptor agonist or antagonist are also presented.

Claims (15)

1. A composition comprising:

a collagen-binding polypeptide segment covalently linked to a PTH/PTHrP receptor agonist;

wherein the collagen-binding polypeptide segment is a bacterial collagen binding polypeptide segment, wherein the PTH/PTHrP receptor agonist comprises residues 1-14 of SEQ ID NO: 1, and wherein the collagen-binding polypeptide segment comprises a polypeptide fragment consisting of at least 10 consecutive amino acids of residues 38-158 of SEQ ID NO: 1.

2. The composition of claim 1 , wherein the collagen-binding polypeptide segment and the PTH/PTHrP receptor agonist are chemically cross-linked to each other or are polypeptide portions of a fusion protein.

3. The composition of claim 1 , wherein the composition has at least 50% greater activity than PTH(1-34) as measured by increased bone mineral density after eight weeks of weekly administration of the composition to a subject in need thereof at equal molar doses of the PTH.

4. The composition of claim 1 , wherein the PTH/PTHrP receptor agonist is a polypeptide and the N-terminus of the collagen-binding polypeptide segment is linked directly or through a linker polypeptide segment to the C-terminus of the PTH/PTHrP receptor agonist polypeptide.

5. The composition of claim 1 , wherein the PTH/PTHrP receptor agonist comprises residues 1-33 of SEQ ID NO: 1, SEQ ID NO: 7, or residues 1-34 of SEQ ID NO: 7.

6. The composition of claim 1 , wherein the composition further comprises residues 37-130 of SEQ ID NO: 2 covalently linked to the collagen-binding polypeptide segment and the PTH/PTHrP receptor agonist.

7. A method of treating a medical condition comprising administering an effective amount of the composition of claim 1 to a mammal in need of treatment for the medical condition, wherein the medical condition is selected from the group consisting of promoting bone growth, promoting hair growth, promoting tissue growth, promoting immune reconstitution, promoting bone marrow stem cell mobilization and treating myocardial infarction.

8. The method of claim 7 , wherein administering the composition to the mammal increases trabecular bone mineral density or cortical bone mineral density or trabecular bone mineral volume or cortical bone mineral volume.

9. The method of claim 7 , wherein the composition is administered before, during or after administration of an implant or in combination with an implant.

10. The method of claim 7 , wherein the implant is a dental implant or a bone graft.

11. The method of claim 7 , wherein the implant comprises intact bone, bone cement, hydroxyapatite, demineralized bone, osteoblasts or combinations thereof.

12. The method of claim 7 , wherein the composition is administered by injection.

13. The method of claim 7 , wherein the composition is administered in aqueous solution at pH below about 5.0.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2019
From: SAKON, JOSHUA
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS
Reel/Frame 050329/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2019
From: PONNAPAKKAM, TULASI; GENSURE, ROBERT C.
To: OCHSNER CLINIC FOUNDATION
Reel/Frame 050329/0148 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2019
From: MATSUSHITA, OSAMU
To: NATIONAL UNIVERSITY CORPORATION KAGAWA UNIVERSITY
Reel/Frame 050329/0254 →
Continuity (7)
Continuation 16249540 · Jan 16, 2019
Continuation 15387817 · Dec 22, 2016
Continuation 14743629 · Jun 18, 2015
Division 13898058 · May 20, 2013
Division 12594547
Provisional Application 60922433 · Apr 9, 2007
Related Publication 20190338010A1 · Nov 7, 2019
Cited By (1)
US 12,403,179