CPC C07K 16/2863 (2013.01) [A61K 31/7088 (2013.01); A61K 31/713 (2013.01); A61K 47/60 (2017.08); A61K 47/6807 (2017.08); A61K 47/6851 (2017.08); A61K 47/6889 (2017.08); A61K 48/0033 (2013.01); A61K 48/005 (2013.01); A61K 48/0075 (2013.01); A61P 35/00 (2018.01); A61P 35/02 (2018.01); C07K 16/2851 (2013.01); C07K 16/30 (2013.01); C07K 16/3061 (2013.01); C12N 15/113 (2013.01); C12N 15/1135 (2013.01); C12N 15/1138 (2013.01); C12N 15/88 (2013.01); A61K 2039/505 (2013.01); C07K 2317/21 (2013.01); C07K 2317/24 (2013.01); C07K 2317/55 (2013.01); C07K 2317/569 (2013.01); C07K 2317/622 (2013.01); C12N 2310/14 (2013.01); C12N 2310/315 (2013.01); C12N 2310/321 (2013.01); C12N 2310/3231 (2013.01); C12N 2310/332 (2013.01); C12N 2310/3513 (2013.01); C12N 2310/3515 (2013.01); C12N 2320/32 (2013.01)] | 23 Claims |
1. A method of treating a disease or disorder in a patient in need thereof, comprising administering to said patient a composition comprising a molecule of Formula (I):
A-X1—B—X2—C Formula I
wherein,
A is an antibody or antigen binding fragment thereof;
B consists of a double-stranded polynucleotide consisting of a passenger strand and a guide strand;
C is a polymer;
X1 is a bond or first non-polymeric linker; and
X2 is a bond or second non-polymeric linker;
wherein the double-stranded polynucleotide comprises at least one 2′ modified nucleotide, at least one modified internucleotide linkage, or at least one inverted abasic moiety; and
wherein A and C are attached in the same strand, but not attached to B at the same terminus.
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