IP Library Granted Patent US 11,904,052
Granted Patent B2
US 11,904,052 · App. 17/749,657 · Granted Feb 20, 2024

Methods for ameliorating infusion reactions

Inventors: Jeffrey P. Bechard (Surrey, CA); Wayne J. Wallis (Seattle, WA)
Assignee: ARBUTUS BIOPHARMA CORPORATION
A61K9/127A61K9/0019A61K31/192A61K47/10A61K47/24A61P29/00C12N15/111A61K45/06
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Quick Facts
Patent No.
US 11,904,052
App. No.
17/749,657
Granted
Feb 20, 2024
Kind
B2
Abstract

Certain embodiments of the invention provide methods of ameliorating an infusion reaction in a mammal in need thereof.

Claims (13)

1. A method of ameliorating an infusion reaction associated with intravenous administration of at least one lipid formulated therapeutic agent in a mammal in need thereof, comprising administering to the mammal via injection a therapeutically effective amount of a nonsteroidal anti-inflammatory (NSAID) in combination with the lipid formulated therapeutic agent being intravenously administered, wherein the NSAID is ketorolac, wherein the lipid formulated therapeutic agent is formulated in a lipid nanoparticle (LNP), which LNP comprises the lipid formulated therapeutic agent, a cationic lipid, and a non-cationic lipid, and wherein the lipid formulated therapeutic agent is a nucleic acid, a polypeptide or an organic compound.

2. The method of claim 1 , wherein the infusion reaction comprises hypertension and/or hypotension.

3. The method of claim 2 , wherein the infusion reaction comprises hypertension followed by hypotension.

4. The method of claim 1 , wherein the infusion reaction comprises an increase in plasma thromboxane B2 levels.

5. The method of claim 1 , wherein the administration of the NSAID begins within about 2 hours prior to the administration of the at least one lipid formulated therapeutic agent.

6. The method of claim 1 , wherein the NSAID is ketorolac and is administered in a dose of about 15 mg to about 60 mg.

7. The method of claim 1 , wherein the NSAID is ketorolac and is administered in a dose of about 30 mg to about 60 mg.

8. The method of claim 1 , wherein the lipid formulated therapeutic agent is an antibody, siRNA or mRNA.

9. The method of claim 8 , wherein the lipid formulated therapeutic agent is siRNA.

10. The method of claim 8 , wherein the lipid formulated therapeutic agent is mRNA.

11. The method of claim 1 , further comprising administering an additional therapeutic agent.

12. The method of claim 11 , wherein the additional therapeutic agent is dexamethasone.

13. The method of claim 1 , wherein the NSAID is administered parenterally, intravenously, intramuscularly or subcutaneously.

Assignments (2)
MERGER Recorded Jun 14, 2022
From: PROTIVA BIOTHERAPEUTICS, INC.
To: ARBUTUS BIOPHARMA CORPORATION
Reel/Frame 060384/0113 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 23, 2022
From: BECHARD, JEFFREY P.; WALLIS, WAYNE J.
To: PROTIVA BIOTHERAPEUTICS, INC.
Reel/Frame 059983/0822 →
Continuity (3)
Continuation 16470490
Provisional Application 62437537 · Dec 21, 2016
Related Publication 20230060006A1 · Feb 23, 2023