| CPC A61K 39/0011 (2013.01) [A61K 38/10 (2013.01); A61K 38/17 (2013.01); A61K 38/177 (2013.01); A61K 38/18 (2013.01); A61K 40/19 (2025.01); A61K 40/24 (2025.01); A61K 40/42 (2025.01); A61K 40/4273 (2025.01); A61K 40/4277 (2025.01); A61K 47/42 (2013.01); A61K 47/64 (2017.08); A61K 47/6425 (2017.08); A61K 47/6803 (2017.08); A61K 47/6811 (2017.08); A61K 47/6865 (2017.08); A61P 1/00 (2018.01); A61P 35/00 (2018.01); C07K 7/06 (2013.01); C07K 7/08 (2013.01); C07K 14/47 (2013.01); C07K 14/475 (2013.01); C07K 19/00 (2013.01); C12N 5/10 (2013.01); A61K 2039/5154 (2013.01); A61K 2039/6031 (2013.01); C07K 2319/02 (2013.01); C07K 2319/03 (2013.01); C07K 2319/10 (2013.01); C07K 2319/33 (2013.01); C07K 2319/40 (2013.01); C12N 2710/16233 (2013.01); Y02A 50/30 (2018.01)] | 26 Claims |
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1. A method for treating glioma in a subject in need thereof, the method comprising administering to the subject a complex comprising:
a) a cell penetrating peptide having an amino acid sequence consisting of SEQ ID NO: 6 (CPP/Z13);
b) at least one antigen or antigenic epitope, wherein the at least one antigen or antigenic epitope comprises at least one tumor epitope; and
c) at least one TLR peptide agonist, wherein the TLR peptide agonist is a TLR2 or TLR4 peptide agonist, having an amino acid sequence consisting of SEQ ID NO: 15,
wherein the components a)-c) are covalently linked.
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