US2021113682A1PendingUtilityA1
Method of providing safe administration of adenoviral vectors encoding a zika virus antigen
Assignee: JANSSEN PHARMACEUTICALS INCPriority: Nov 20, 2017Filed: Nov 11, 2020Published: Apr 22, 2021
Est. expiryNov 20, 2037(~11.3 yrs left)· nominal 20-yr term from priority
A61K 9/0019A61K 2039/6075A61K 47/6901A61P 31/14C12N 2710/10343C12N 2770/24134A61K 39/12Y02A50/30
55
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Claims
Abstract
Provided are methods for generating an immune response against a Zika virus in a human subject in need thereof. The methods comprise administering to the subject a pharmaceutical composition comprising adenoviral vectors encoding a Zika virus antigen and a pharmaceutically acceptable carrier.
Claims
exact text as granted — not AI-modifiedIt is claimed:
1 . A method for generating an immune response against a Zika virus in a human subject in need thereof, the method comprising administering to the subject a pharmaceutical composition comprising adenoviral vectors comprising a nucleic acid sequence encoding a Zika virus antigen, wherein the Zika virus antigen comprises the amino acid sequence of SEQ ID NO:2, and a pharmaceutically acceptable carrier, wherein about 1×10 11 adenoviral vectors are administered in a single dose to the human subject in need thereof.
2 . The method of claim 1 , wherein the pharmaceutical composition is administered via an intramuscular injection to the subject in need thereof.
3 . The method of claim 1 , wherein the immune response is a protective immune response against a Zika virus.
4 . The method of claim 1 , wherein the adenoviral vectors are of the Ad26 serotype.
5 . A method for preventing a Zika virus infection or the progression of a Zika virus infection in a human subject in need thereof, the method comprising administering to the subject a pharmaceutical composition comprising adenoviral vectors comprising a nucleic acid sequence encoding a Zika virus antigen, wherein the Zika virus antigen comprises the amino acid sequence of SEQ ID NO:2, and a pharmaceutically acceptable carrier, wherein about 1×10 11 adenoviral vectors are administered in a single dose to the human subject in need thereof.
6 . The method of claim 5 , wherein the pharmaceutical composition is administered via an intramuscular injection to the subject in need thereof.
7 . The method of claim 5 , wherein the adenoviral vectors are of the Ad26 serotype.Join the waitlist — get patent alerts
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