CPC A61K 48/0066 (2013.01) [A61K 9/0019 (2013.01); A61K 9/1271 (2013.01); A61K 9/5123 (2013.01); A61K 9/5146 (2013.01); A61K 31/7088 (2013.01); A61K 31/7105 (2013.01); A61K 31/711 (2013.01); A61K 31/7115 (2013.01); A61K 31/712 (2013.01); A61K 39/0011 (2013.01); A61K 39/12 (2013.01); A61K 39/215 (2013.01); A61K 48/0033 (2013.01); A61P 31/14 (2018.01); A61P 35/00 (2018.01); B82Y 5/00 (2013.01); C12N 7/00 (2013.01); C12N 15/11 (2013.01); C12N 15/67 (2013.01); C12N 15/88 (2013.01); C12P 19/34 (2013.01); A61K 38/00 (2013.01); A61K 2039/53 (2013.01); A61K 2039/54 (2013.01); A61K 2039/545 (2013.01); A61K 2039/55555 (2013.01); C12N 2770/18022 (2013.01); C12N 2770/18034 (2013.01); C12N 2770/18071 (2013.01); C12N 2770/20034 (2013.01); C12N 2840/00 (2013.01)] | 49 Claims |
1. A composition or medical preparation comprising an RNA polynucleotide comprising a sequence encoding a payload, wherein:
the RNA polynucleotide optionally comprises a modified uridine in place of one or more uridines; and
the 5′ terminus of the RNA polynucleotide comprises m7(3′OMeG)(5′)ppp(5′)(2′OMeA1)pG2pA3pA4pN5, wherein N5 is uridine or a modified uridine.
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