US2009081244A1PendingUtilityA1

Dry Formulation for Transcutaneous Immunization

Assignee: US ARMYPriority: Nov 14, 1996Filed: Jan 25, 2008Published: Mar 26, 2009
Est. expiryNov 14, 2016(expired)· nominal 20-yr term from priority
A61P 33/00A61K 2039/545A61P 31/04A61K 39/104A61K 39/107C12N 2760/20134A61K 2039/55533A61K 39/099C12N 2760/16234A61K 39/05A61K 2039/55544A61K 2039/5252A61K 2039/53A61P 31/10A61K 39/102A61K 39/015A61K 2039/70A61K 2039/55561A61K 39/0258A61K 2039/55555A61K 39/116A61K 39/08A61K 39/008A61K 2039/55522A61K 2039/55505C12N 2740/16234A61P 37/04A61K 2039/54A61K 39/12A61P 31/16C12N 2760/16134Y02A50/30
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Claims

Abstract

A transcutaneous immunization system delivers antigen to immune cells through the skin, and induces an immune response in an animal or human. For example, skin-active adjuvant (e.g., an ADP-ribosylating exotoxin) can be used to induce an antigen-specific immune response (e.g., humoral and/or cellular effectors) after transcutaneous application of a dry formulation containing antigen and adjuvant to skin of the animal or human. The dry formulation may be a powder or a unit-dose patch. Use of adjuvant is not required if the antigen is sufficiently antigenic. Transcutaneous immunization may be induced with or without penetration enhancement

Claims

exact text as granted — not AI-modified
1 - 69 . (canceled) 
     
     
         70 . A method of inducing an antigen-specific immune response to an antigen comprising applying a formulation to skin of a subject, wherein the formulation comprises an antigen, wherein the formulation is applied in dry form. 
     
     
         71 . The method of  claim 70 , wherein the formulation further comprises an adjuvant.

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