The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 09, 2021

Filed:

Nov. 13, 2017
Applicant:

Variation Biotechnologies Inc., Ottawa, CA;

Inventor:

David E. Anderson, Boston, MA (US);

Assignee:
Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
A61K 47/28 (2006.01); A61K 39/12 (2006.01); A61K 39/39 (2006.01); A61K 39/205 (2006.01); A61K 47/14 (2017.01); C12N 7/00 (2006.01); A61K 47/24 (2006.01); A61K 39/00 (2006.01);
U.S. Cl.
CPC ...
A61K 47/28 (2013.01); A61K 39/12 (2013.01); A61K 39/205 (2013.01); A61K 39/39 (2013.01); A61K 47/14 (2013.01); A61K 47/24 (2013.01); C12N 7/00 (2013.01); A61K 2039/55555 (2013.01); A61K 2039/55566 (2013.01); C12N 2760/20134 (2013.01); C12N 2760/20171 (2013.01); Y02A 50/30 (2018.01);
Abstract

The present disclosure provides compositions and methods useful for treating viral infections. As described herein, the compositions and methods are based on the development of immunogenic compositions that include an inactivated virus in combination with a non-ionic surfactant vesicle (NISV). In certain embodiments at least a portion of the antigen present in the composition is physically associated with the NISV. In certain embodiments the compositions are lyophilized and subsequently rehydrated after a period of storage. In certain embodiments the rehydrated compositions exhibit greater potency as compared to otherwise equivalent compositions that lack the NISV. In certain embodiments the lyophilized compositions are stored at temperatures in excess of 8° C. prior to rehydration. In certain embodiments, the rehydrated compositions exhibit greater potency as compared to otherwise equivalent compositions that lack the NISV and that were also stored at temperatures in excess of 8° C. prior to rehydration. In certain embodiments the antigen is taken from a licensed vaccine and the administered dose of antigen is less than the standard human dose for the licensed vaccine.


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