IP Library Granted Patent US 10,940,188
Granted Patent B2
US 10,940,188 · App. 16/779,132 · Granted Mar 9, 2021

Compounds and methods for treatment and prevention of Flavivirus infection

Inventors: Hengli Tang (Tallahassee, FL); Emily M. Lee (Tallahassee, FL); Yichen Cheng (Tallahassee, FL); Yi Zhou (Tallahassee, FL); Wei Zheng (Rockville, MD); Ruili Huang (Rockville, MD); Miao Xu (Rockville, MD); Wenwei Huang (Rockville, MD); Menghang Xia (Rockville, MD); Hongjun Song (Baltimore, MD); Guo-Li Ming (Baltimore, MD); Zhexing Wen (Atlanta, GA)
Assignees: FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC.; THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; THE JOHNS HOPKINS UNIVERSITY
A61K38/55A61K31/24A61K31/609A61K38/43A61K45/06C07C239/02C07C239/08A61K38/00Y02A50/30
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Quick Facts
Patent No.
US 10,940,188
App. No.
16/779,132
Granted
Mar 9, 2021
Kind
B2
Abstract

The present invention concerns the use of compounds for the treatment or prevention of Flavivirus infections, such as Zika virus infections. Aspects of the invention include methods for treating or preventing Flavivirus virus infection, such as Zika virus infection, by administering a compound or class of compound disclosed herein, such as a niclosamide compound, an emricasan compound, a cyclin-dependent kinase inhibitor, a proteasome inhibitor, or a combination of two or more of the foregoing, to a subject in need thereof; methods for inhibiting Flavivirus infections such as Zika virus infections in a cell in vitro or in vivo; pharmaceutical compositions; packaged dosage formulations; and kits for treating or preventing Flavivirus infections, such Zika virus infections.

Claims (18)

1. A method for treating or preventing Zika virus infection in a human or non-human animal subject, said method comprising administering an effective amount of emetine, or a pharmaceutically acceptable salt thereof, to a subject in need thereof.

2. The method of claim 1 , wherein the subject has the Zika virus infection at the time of said administering, and the emetine or pharmaceutically acceptable salt thereof is administered as therapy.

3. The method of claim 2 , further comprising, prior to said administering, identifying the subject as having the Zika virus infection.

4. The method of claim 3 , wherein said identifying comprises assaying a biological sample obtained from the subject for the presence of Zika virus nucleic acids or Zika virus proteins.

5. The method of claim 4 , wherein said assaying comprises use of reverse transcriptase-polymerase chain reaction (RT-PCR), immunological assay, or Plaque-reduction neutralization testing (PRNT).

6. The method of claim 1 , wherein the subject does not have the Zika virus infection at the time of said administering, and the emetine or pharmaceutically acceptable salt thereof is administered as prophylaxis.

7. The method of claim 1 , wherein the emetine or pharmaceutically acceptable salt thereof is administered orally, nasally, rectally, parenterally, subcutaneously, intramuscularly, or intravascularly.

8. The method of claim 1 , further comprising administering an additional agent for treating or preventing Zika virus infection, or a symptom thereof, in the same formulation as the emetine or pharmaceutically acceptable salt thereof, or in a separate formulation before, during, or after administration of the emetine or pharmaceutically acceptable salt thereof.

9. The method of claim 1 , wherein said administering comprises administering a composition to the subject, wherein the composition comprises the emetine or pharmaceutically acceptable salt thereof and a pharmaceutically acceptable buffer, carrier, or diluent.

10. The method of claim 1 , wherein the subject is human.

11. The method of claim 1 , wherein the subject is human, wherein the human subject has the Zika virus infection at the time of said administering, and the emetine or pharmaceutically acceptable salt thereof is administered as therapy.

12. A method for inhibiting Zika virus infection in human or non-human animal cells in vitro or in vivo, said method comprising contacting an effective amount of emetine, or a pharmaceutically acceptable salt thereof, to a human or non-human animal cell in vitro or in vivo before or after exposure of the cell to Zika virus.

13. The method of claim 12 , wherein the human or non-human animal cell is a human cell.

14. The method of claim 12 , wherein said contacting is done in vivo.

15. The method of claim 12 , wherein said contacting is done in vitro.

16. The method of claim 12 , wherein said contacting is done before exposure of the cell to the Zika virus.

17. The method of claim 12 , wherein said contacting is done after exposure of the cell to the Zika virus.

18. The method of claim 12 , wherein the human or non-animal cell is a human cell, wherein said contacting is done in vivo, and wherein said contacting is done after exposure of the cell to the Zika virus.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Apr 5, 2024
From: ZEVRA THERAPEUTICS INC. (AS SUCCESSOR IN INTEREST TO NANTAHALA CAPITAL MANAGEMENT, LLC, AS SUCCESSOR IN INTEREST TO SWK FUNDING LLC)
To: ACER THERAPEUTICS INC.
Reel/Frame 067020/0036 →
SECURITY INTEREST Recorded Jul 6, 2023
From: SWK FUNDING LLC; ACER THERAPEUTICS INC
To: NANTAHALA CAPITAL MANAGEMENT, LLC
Reel/Frame 064167/0828 →
SECURITY INTEREST Recorded Mar 11, 2022
From: ACER THERAPEUTICS INC.
To: SWK FUNDING LLC
Reel/Frame 059237/0638 →