MUSCLE TARGETING COMPLEXES AND FORMULATIONS FOR TREATING MYOTONIC DYSTROPHY
Aspects of the disclosure relate to complexes and other aspects relate to formulations (e.g., aqueous, lyophilized forms) comprising such complexes comprising an oligonucleotide (e.g., useful for targeting DMPK) covalently linked to an antibody (e.g., anti-TfR1 antibody).
1 - 23 . (canceled)
24 . A complex comprising a structure of formula (I): [R 1 ] n1 —R 2 , wherein each R 1 comprises a group of the formula (Ia):
wherein R 3 comprises an oligonucleotide comprising a structure of +C*+A*OG*oC*dG*dC*dC*dC*dA*dC*dC*dA*oG*OU*+C*+A (SEQ ID NO: 21), wherein for each nucleoside, N, of the oligonucleotide, +N represents an LNA ribonucleoside, dN represents a 2′-deoxyribonucleoside, oN represents a 2′-O-methoxyethyl (MOE) modified ribonucleoside, oC represents a 5-methyl-2′-MOE-cytidine, +C represents a 5-methyl-2′-4′-bicyclic-cytidine, wherein the 2′ and 4′ positions of the sugar are bridged via a methylene, oU represents a 5-methyl-2′-MOE-uridine, and wherein * represents a phosphorothioate internucleoside linkage;
wherein R 2 comprises a Fab comprising a heavy chain comprising the amino acid sequence of SEQ ID NO: 19 and a light chain comprising the amino acid sequence of SEQ ID NO: 20;
wherein R 1 is covalently linked at attachment point A to R 2 , wherein n1 is an integer representing the number of instances of R 1 , and wherein each instance of R 1 is covalently linked to a different amino acid residue of the Fab.
25 . The complex of claim 24 , wherein each different amino acid residue is a lysine.
26 . The complex of claim 24 , wherein the heavy chain of the Fab comprises an N-terminal pyroglutamate.
27 . The complex of claim 24 , wherein n1 is 1-5.
28 . A composition comprising the complex of claim 24 .
29 . The composition of claim 28 , wherein the oligonucleotide is in a salt form.
30 . The composition of claim 29 , wherein the oligonucleotide is in a sodium salt form, potassium salt form, or magnesium salt form.
31 . The composition of claim 28 , wherein each different amino acid residue is a lysine.
32 . The composition of claim 28 , wherein the heavy chain of the Fab comprises an N-terminal pyroglutamate.
33 . The composition of claim 28 , wherein the composition is formulated for intravenous administration.
34 . A method of reducing DMPK expression in a subject, the method comprising administering to the subject an effective amount of a composition comprising the complex of claim 24 .
35 . A method of treating myotonic dystrophy in a subject, the method comprising administering to the subject an effective amount of a composition comprising the complex of claim 24 .
36 . The method of claim 35 , wherein the subject has an expansion of a disease-associated repeat of a DMPK allele that is associated with myotonic dystrophy.
37 . The method of claim 36 , wherein the disease-associated repeat comprises repeating units of a CTG trinucleotide sequence.
38 . The method of claim 34 , wherein each different amino acid residue is a lysine.
39 . The method of claim 34 , wherein the heavy chain of the Fab comprises an N-terminal pyroglutamate.
40 . The method of claim 34 , wherein the composition is formulated for intravenous administration.
41 . The method of claim 34 , wherein the subject is human.
42 . The method of claim 35 , wherein each different amino acid residue is a lysine.
43 . The method of claim 35 , wherein the heavy chain of the Fab comprises an N-terminal pyroglutamate.
44 . The method of claim 35 , wherein the composition is formulated for intravenous administration.
45 . The method of claim 35 , wherein the subject is human.