IP Library Granted Patent US 10,456,448
Granted Patent B2
US 10,456,448 · App. 14/773,167 · Granted Oct 29, 2019

PTD-SMAD7 therapeutics

Inventors: Xiao-Jing Wang (Greenwood Village, CO); Qinghong Zhang (Englewood, CO); Yosef Refaeli (Denver, CO)
Assignee: The Regents of the University of Colorado, a body corporate
A61K38/18A61K38/162C07K14/005C07K14/4702C07K14/4703C07K14/475C12N7/00A61K38/00A61K48/005C07K2319/10C07K2319/20C07K2319/23C12N2740/16311C12N2740/16322C12N2800/22
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Quick Facts
Patent No.
US 10,456,448
App. No.
14/773,167
Granted
Oct 29, 2019
Kind
B2
Abstract

The present technology provides methods and compositions for the treatment of inflammatory and/or tissue damage conditions. In particular, the use of Smad7 compositions delivered locally or systemically to a site of inflammation and/or tissue damage is described. Other specific embodiments concern treatment or prevention of side effects caused by radiation and/or chemotherapy, including but not limited to oral and gastric mucositis. Also provided are codon-optimized nucleic acids encoding for Smad7 fusion proteins.

Claims (32)

1. A protein molecule comprising a protein transduction domain and a human mothers against decapentaplegic-7 protein (Smad7) fragment comprising amino acids 203-258 of the human Smad7 protein, wherein the Smad7 fragment retains one or more biological activities of the functional full-length Smad7 protein, and with the proviso that the protein molecule lacks at least amino acids 1 to 25 of the human Smad7 protein.

2. The protein molecule of claim 1 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting wound healing, and treating inflammatory and auto-immune diseases and auto-immune disorders.

3. The protein molecule of claim 2 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting healing in oral mucositis, ulcers, diabetic wounds, and radiation-induced damage; reducing scarring and fibrosis; and treating psoriasis and inflammatory disorders.

4. The protein molecule of claim 1 , wherein the protein transduction domain is Tat.

5. The protein molecule of claim 1 , wherein the protein molecule comprises amino acids 203-426 of the human Smad7 protein.

6. The protein molecule of claim 5 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting wound healing, and treating inflammatory and auto-immune diseases and auto-immune disorders.

7. The protein molecule of claim 5 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting healing in oral mucositis, ulcers, diabetic wounds, and radiation-induced damage; reducing scarring and fibrosis; and treating psoriasis and inflammatory disorders.

8. The protein molecule of claim 5 , wherein the protein transduction domain is Tat.

9. A pharmaceutical composition comprising the protein molecule of claim 1 , and one or more pharmaceutically acceptable excipients.

10. A pharmaceutical composition comprising the protein molecule of claim 5 , and one or more pharmaceutically acceptable excipients.

11. A protein molecule comprising a protein transduction domain and a human mothers against decapentaplegic-7 protein (Smad7) fragment comprising amino acids 203-217 of the human Smad7 protein, wherein the Smad7 fragment retains one or more biological activities of the functional full-length Smad7 protein, and with the proviso that the protein molecule lacks at least amino acids 1 to 25 of the human Smad7 protein.

12. The protein molecule of claim 11 , wherein the protein transduction domain is Tat.

13. The protein molecule of claim 11 , wherein the protein molecule has one or more biological activity selected from the group consisting of promoting wound healing, and treating inflammatory and auto-immune diseases and auto-immune disorders.

14. The protein molecule of claim 13 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting healing in oral mucositis, ulcers, diabetic wounds, and radiation-induced damage; reducing scarring and fibrosis; and treating psoriasis and inflammatory disorders.

15. A pharmaceutical composition comprising the protein molecule of claim 11 , and one or more pharmaceutically acceptable excipients.

16. A protein molecule comprising a protein transduction domain and a human mothers against decapentaplegic-7 protein (Smad7) fragment consisting of amino acids 203-258 of the human Smad7 protein.

17. The protein molecule of claim 16 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting wound healing, and treating inflammatory and auto-immune diseases and auto-immune disorders.

18. The protein molecule of claim 17 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting healing in oral mucositis, ulcers, diabetic wounds, and radiation-induced damage; reducing scarring and fibrosis; and treating psoriasis and inflammatory disorders.

19. The protein molecule of claim 16 , wherein the protein transduction domain is Tat.

20. A pharmaceutical composition comprising the protein molecule of claim 16 , and one or more pharmaceutically acceptable excipients.

21. A protein molecule comprising a protein transduction domain and a human mothers against decapentaplegic-7 protein (Smad7) fragment consisting of amino acids 203-217 of the human Smad7 protein.

22. The protein molecule of claim 21 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting wound healing, and treating inflammatory and auto-immune diseases and auto-immune disorders.

23. The protein molecule of claim 22 , wherein the protein molecule has one or more biological activities selected from the group consisting of promoting healing in oral mucositis, ulcers, diabetic wounds, and radiation-induced damage; reducing scarring and fibrosis; and treating psoriasis and inflammatory disorders.

24. The protein molecule of claim 21 , wherein the protein transduction domain is Tat.

25. A pharmaceutical composition comprising the protein molecule of claim 21 , and one or more pharmaceutically acceptable excipients.

26. A protein molecule comprising a protein transduction domain and a human mothers against decapentaplegic-7 protein (Smad7) fragment consisting of amino acids 203-426 of the human Smad7 protein, wherein the Smad7 fragment retains one or more biological activities of the functional full-length Smad7 protein.

27. A method for treating an inflammatory condition in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the protein molecule of claim 11 .

28. A method for treating a disease or disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the protein of claim 11 , wherein the administration of the protein results in an increase in one or more of cell proliferation or cell migration, or reducing one or more of apoptosis or DNA damage in the subject.

29. A method for treating an inflammatory condition in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 9 .

30. A method for treating a disease or disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 9 , wherein the administration of the protein results in an increase in one or more of cell proliferation or cell migration, or reducing one or more of apoptosis or DNA damage in the subject.

31. A method for treating an inflammatory condition in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 15 .

32. A method for treating a disease or disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 15 , wherein the administration of the protein results in an increase in one or more of cell proliferation or cell migration, or reducing one or more of apoptosis or DNA damage in the subject.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 18, 2018
From: UNIVERSITY OF COLORADO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046900/0049 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2017
From: WANG, XIAO-JING; ZHANG, QINGHONG; REFAELI, YOSEF
To: THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE
Reel/Frame 042721/0574 →
Continuity (2)
Provisional Application 61775252 · Mar 8, 2013
Related Publication 20160039894A1 · Feb 11, 2016