METHOD OF TREATING DUCHENNE MUSCULAR DYSTROPHY
Provided herein are methods of treating or delaying the onset of Duchenne muscular dystrophy using modified antisense oligonucleotides.
1 . A method of treating a subject having DMD or delaying the onset of DMD in a subject, comprising administering to the subject AON1 at a dose of 0.4 mg/kg, 0.6 mg/kg, 0.8 mg/kg, 1.5 mg/kg, 3 mg/kg, 6 mg/kg, 9 mg/kg, 12 mg/kg or 18 mg/kg, wherein the AON1 is administered QW.
2 . The method of claim 1 , wherein the AON1 is administered QWx15, 16, 17, 18, 19, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34 or 35W.
3 . The method of claim 1 , wherein the AON1 is administered QWx24W or QWx25W.
4 . The method of claim 3 , wherein the AON1 is administered QWx25W.
5 . The method of claim 3 , wherein the AON1 is administered QWx24W.
6 . The method of claim 1 , wherein the AON1 is administered at a dose of 3 mg/kg.
7 . The method of claim 1 , wherein the AON1 is administered at a dose of 6 mg/kg.
8 . The method of claim 1 , wherein the AON1 is administered at a dose of 9 mg/kg.
9 . The method of claim 1 , wherein the AON1 is administered at a dose of 12 mg/kg.
10 . The method of claim 1 , wherein the AON1 is administered at a dose of 18 mg/kg.
11 . The method of claim 1 , that is a method of treating DMD in a subject.
12 . The method of claim 1 , that is a method of delaying the onset of DMD in a subject.
13 . The method of claim 1 , further comprising administering to the subject a second active agent.
14 . The method of claim 13 , wherein the second active agent is eteplirsen, casimersen, golodirsen, viltolarsen, SRP-5051 (Sarepta Therapeutics), a corticosteroid such as deflazacort, a gene therapy (e.g., SRP-9001, GALGT2 or GNT 0004 (Sarepta Therapeutics)), gene editing (e.g., CRISPR/CAS9 (Sarepta Therapeutics)) or a cellular therapy (e.g., CAP-1002 (Capricor Therapeutics/Nippon Shinyaku Co. Ltd.)).