US2018280490A1PendingUtilityA1

Methods and compositions for preventing a condition

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Assignee: CYVAX INCPriority: Aug 9, 2010Filed: Mar 20, 2018Published: Oct 4, 2018
Est. expiryAug 9, 2030(~4.1 yrs left)· nominal 20-yr term from priority
Inventors:Richard Markham
A61P 37/04A61P 37/02A61P 25/28A61P 31/12A61P 35/00A61P 31/04A61P 33/06A61P 33/00A61P 31/10A61K 2039/55522A61K 2039/53A61K 39/015A61K 39/39A61K 31/713A61K 2039/6031A61K 31/7105A61P 25/00Y02A50/412A61K 39/0011A61K 39/295C12N 15/62Y02A50/30
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Claims

Abstract

Provided herein are methods, compositions, and kits for preventing, inhibiting, reducing the severity of, or treating a disease or condition. A pharmaceutical composition provided herein can comprise a nucleic acid sequence encoding an antigen fused to an immune cell product, e.g., MIP-3α, and an adjuvant. The antigen can be from a bacteria, virus, fungus, parasite, or cancer. The antigen can be an Alzheimer's disease antigen.

Claims

exact text as granted — not AI-modified
1 .- 98 . (canceled) 
     
     
         99 . A method, comprising:
 administering to a subject having a cancer a nucleic acid encoding a fusion protein, wherein the fusion protein comprises a cancer antigen fused to human macrophage inflammatory protein-3 alpha (MIP-3α);   administering to the subject a CpG oligodeoxynucleotide; and   administering to the subject interferon alpha (IFN-α) or a nucleic acid encoding IFN-α.   
     
     
         100 . The method of  claim 99 , wherein the cancer antigen is a melanoma antigen. 
     
     
         101 . The method of  claim 100 , wherein the melanoma antigen is gp100. 
     
     
         102 . The method of  claim 99 , wherein the nucleic acid is a deoxyribonucleic acid (DNA). 
     
     
         103 . The method of  claim 102 , wherein the DNA is a plasmid DNA. 
     
     
         104 . The method of  claim 99 , wherein the subject is a human subject. 
     
     
         105 . A method, comprising:
 administering to a subject having a cancer a nucleic acid encoding a fusion protein, wherein the fusion protein comprises a cancer antigen fused to human macrophage inflammatory protein-3 alpha (MIP-3α);   administering to the subject a CpG oligodeoxynucleotide; and   administering to the subject a cytokine or a nucleic acid encoding a cytokine.   
     
     
         106 . The method of  claim 105 , wherein the cancer antigen is a melanoma antigen. 
     
     
         107 . The method of  claim 106 , wherein the melanoma antigen is gp100. 
     
     
         108 . The method of  claim 105 , wherein the nucleic acid is a deoxyribonucleic acid (DNA). 
     
     
         109 . The method of  claim 108 , wherein the DNA is a plasmid DNA. 
     
     
         110 . The method of  claim 105 , wherein the cytokine is an interferon. 
     
     
         111 . The method of  claim 105 , wherein the subject is a human subject. 
     
     
         112 . A method, comprising:
 administering to a human subject having a cancer a deoxyribonucleic acid (DNA) encoding a fusion protein, wherein the fusion protein comprises gp100 fused to human macrophage inflammatory protein-3 alpha (MIP-3α);   administering to the subject a CpG oligodeoxynucleotide; and   administering to the subject interferon alpha (IFN-α) or a nucleic acid encoding IFN-α.

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