IP Library Granted Patent US 9,895,411
Granted Patent B2
US 9,895,411 · App. 13/806,250 · Granted Feb 20, 2018

Analogs of C5a and methods of using same

Inventors: Sam D. Sanderson (Omaha, NE); Joy Arlene Phillips (San Diego, CA); Edward Leroy Morgan (San Diego, CA); Marilyn Louise Thoman (San Diego, CA); Tamsin Sheen (San Diego, CA); Kelly S. Doran (San Diego, CA); Elizabeth Louise Virts (Carlsbad, CA); Tammy Kielian (Omaha, NE); Mark Hanke (Seattle, WA)
Assignees: SAN DIEGO STATE UNIVERSITY RESEARCH FOUNDATION; BOARD OF REGENTS OF THE UNIVERSITY OF NEBRASKA
A61K38/08A61K38/10A61K45/06
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Quick Facts
Patent No.
US 9,895,411
App. No.
13/806,250
Granted
Feb 20, 2018
Kind
B2
Abstract

Materials and methods for treating and preventing an infection or disease, and for directly killing microorganisms, using carboxy-terminal C5a analogs, are provided.

Claims (10)

1. A method of treating an infection or disease comprising administering an effective amount of an oligopeptide carboxy-terminal analog of C5a to a mammal, wherein the infection or disease is selected from the group consisting of influenza, Staphylococcus infection, Escherichia coli infection, Streptococcus infection, and biofilm, said analog not attached to an antigen, and said analog being a C5a receptor agonist having response-selective C5a receptor binding activity, said binding activity comprising activation of antigen presenting cells, wherein the analog is Tyr-Ser-Phe-Lys-Asp-Met-Pro-MeL-(D-Ala)-Arg (SEQ ID NO: 4).

2. The method according to claim 1 wherein the analog is administered by a route selected from the group consisting of oral, topical, inhalation spray, intradermal, subcutaneous injection, and intravenous injection.

3. The method according to claim 1 wherein the analog is formulated in a powder, aerosol, cream, gel, liquid, bandage, and surgical suture.

4. The method according to claim 1 wherein the analog is administered at a dose of 25 μg to 500 μg.

5. The method according to claim 1 wherein the analog is administered concurrently, prior, or following administration of a second therapeutic agent.

6. The method according to claim 5 wherein the second therapeutic agent is selected from the group consisting of vaccine, antibiotic, antifungal, and antiparasitic.

7. The method according to claim 6 wherein the vaccine is a C-terminal analog of C5a attached to an antigen.

8. The method according to claim 1 wherein the mammal is a human selected from the group consisting of: fetus, newborn, infant, child, young adult, adult, elder, and immunocompromised.

9. A method of treating an influenza infection comprising administering an effective amount of C5a analog EP67 to a mammal, said analog not attached to an antigen.

10. A method of treating a dermal Staphylococcus infection comprising administering an effective amount of C5a analog, EP67, to a mammal, said analog not attached to an antigen.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2013
From: DORAN, KELLY; MORGAN, EDWARD; PHILLIPS, JOY; SHEEN, TAMSIN; THOMAN, MARILYN; VIRTS, ELIZABETH
To: SAN DIEGO STATE UNIVERSITY RESEARCH FOUNDATION
Reel/Frame 031618/0566 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2013
From: SANDERSON, SAM D.; KIELIAN, TAMMY; HANKE, MARK
To: BOARD OF REGENTS OF THE UNIVERSITY OF NEBRASKA
Reel/Frame 031618/0646 →
CONFIRMATORY LICENSE Recorded Feb 20, 2013
From: UNIVERSITY OF NEBRASKA MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029839/0109 →
Continuity (2)
Provisional Application 61359444 · Jun 29, 2010
Related Publication 20150297668A1 · Oct 22, 2015