EXON SKIPPING OLIGOMERS AND OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY
Antisense oligomers and antisense oligomer conjugates complementary to a selected target site in the human dystrophin gene to induce exon 53 skipping are described.
1 . An antisense oligomer conjugate of Formula (I):
or a pharmaceutically acceptable salt thereof, wherein:
each Nu is a nucleobase which taken together form a targeting sequence; and
T is a moiety selected from:
and
R 1 is C 1 -C 6 alkyl,
wherein the targeting sequence is complementary to an exon 53 annealing site in the dystrophin pre-mRNA selected from the group consisting of H53A(−100−76), H53A(−95−71), H53A(−90−66), H53A(−85−61), H53A(−80−56), H53A(−75−51), H53A(−70−46), H53A(−65−41), H53A(−60−36), H53A(−55−31), H53A(−50−26), H53A(−45−21), H53A(−40−16), H53A(−35−11), H53A(−30−06), H53A(−25−01), H53A(−24+01), H53A(−23+02), H53A(−22+03), H53A(−21+04), H53A(−20+05), H53A(−19+06), H53A(−18+07), H53A(−17+08), H53A(−16+09), H53A(−15+10), H53A(−14+11), H53A(−13+12), H53A(−12+13), H53A(−11+14), H53A(−10+15), H53A(−9+16), H53A(−8+17), H53A(−7+18), H53A(−6+19), H53A(−5+20), H53A(−4+21), H53A(−3+22), H53A(−2+23), H53A(−1+24), H53D(+24−01), H53D(+23−02), H53D(+22−03), H53D(+21−04), H53D(+20−05), H53D(+19−06), H53D(+18−07), H53D(+17−08), H53D(+16−09), H53D(+15−10), H53D(+14−11), H53D(+13−12), H53D(+12−13), H53D(+11−14), H53D(+10−15), H53D(+9−16), H53D(+8−17), H53D(+7−18), H53D(+6−19), H53D(+5−20), H53D(+4−21), H53D(+3−22), H53D(+2−23), H53D(+1−24), and H53D(−01−25).
2 . The antisense oligomer conjugate of claim 1 , wherein the annealing site is selected from the group consisting of H53A(−45−21), H53A(−40−16), H53A(−35−11), H53A(−25−01), H53A(−24+01), H53A(−23+02), H53A(−22+03), H53A(−21+04), H53A(−20+05), H53A(−19+06), H53A(−18+07), H53A(−17+08), H53A(−16+09), H53A(−15+10), H53A(−14+11), H53A(−13+12), H53A(−12+13), H53A(−11+14), H53A(−10+15), H53A(−8+17), H53A(−7+18), H53A(−6+19), H53A(−5+20), H53A(−2+23), H53A(−1+24), H53D(+24−01), H53D(+23−02), H53D(+22−03), H53D(+21−04), H53D(+20−05), H53D(+19−06), H53D(+17−08), H53D(+16−09), H53D(+13−12), H53D(+12−13) H53D(+7−18), and H53D(+1−24).
3 . The antisense oligomer conjugate of claim 1 , wherein the targeting sequence is selected from the group consisting of SEQ ID NOs: 70-134.
4 . The antisense oligomer conjugate of claim 2 , wherein the targeting sequence is selected from the group consisting of SEQ ID NOs: 81-83, 85-100, 102-104, 108-115, 117, 118, 121, 122, 127, and 133.
5 . The antisense oligomer conjugate of claim 1 , wherein each Nu is independently selected from cytosine (C), guanine (G), thymine (T), adenine (A), 5-methylcytosine (5mC), uracil (U), and hypoxanthine (I).
6 . An antisense oligomer conjugate of Formula (III):
or a pharmaceutically acceptable salt thereof, wherein each Nu is a nucleobase which taken together form a targeting sequence that is complementary to an exon 53 annealing site in the dystrophin pre-mRNA is selected from the group consisting of H53A(−100−76), H53A(−95−71), H53A(−90−66), H53A(−85−61), H53A(−80−56), H53A(−75−51), H53A(−70−46), H53A(−65−41), H53A(−60−36), H53A(−55−31), H53A(−50−26), H53A(−45−21), H53A(−40−16), H53A(−35−11), H53A(−30−06), H53A(−25−01), H53A(−24+01), H53A(−23+02), H53A(−22+03), H53A(−21+04), H53A(−20+05), H53A(−19+06), H53A(−18+07), H53A(−17+08), H53A(−16+09), H53A(−15+10), H53A(−14+11), H53A(−13+12), H53A(−12+13), H53A(−11+14), H53A(−10+15), H53A(−9+16), H53A(−8+17), H53A(−7+18), H53A(−6+19), H53A(−5+20), H53A(−4+21), H53A(−3+22), H53A(−2+23), H53A(−1+24), H53D(+24−01), H53D(+23−02), H53D(+22−03), H53D(+21−04), H53D(+20−05), H53D(+19−06), H53D(+18−07), H53D(+17−08), H53D(+16−09), H53D(+15−10), H53D(+14−11), H53D(+13−12), H53D(+12−13), H53D(+11−14), H53D(+10−15), H53D(+9−16), H53D(+8−17), H53D(+7−18), H53D(+6−19), H53D(+5−20), H53D(+4−21), H53D(+3−22), H53D(+2−23), H53D(+1−24), and H53D(−01−25).
7 . The antisense oligomer conjugate of claim 6 , wherein the annealing site is selected from the group consisting of H53A(−45−21), H53A(−40−16), H53A(−35−11), H53A(−25−01), H53A(−24+01), H53A(−23+02), H53A(−22+03), H53A(−21+04), H53A(−20+05), H53A(−19+06), H53A(−18+07), H53A(−17+08), H53A(−16+09), H53A(−15+10), H53A(−14+11), H53A(−13+12), H53A(−12+13), H53A(−11+14), H53A(−10+15), H53A(−8+17), H53A(−7+18), H53A(−6+19), H53A(−5+20), H53A(−2+23), H53A(−1+24), H53D(+24−01), H53D(+23−02), H53D(+22−03), H53D(+21−04), H53D(+20−05), H53D(+19−06), H53D(+17−08), H53D(+16−09), H53D(+13−12), H53D(+12−13) H53D(+7−18), and H53D(+1−24).
8 . The antisense oligomer conjugate of claim 6 , wherein the targeting sequence is selected from the group consisting of SEQ ID NOs: 70-134.
9 . The antisense oligomer conjugate of claim 7 , wherein the targeting sequence is selected from the group consisting of SEQ ID NOs: 81-83, 85-100, 102-104, 108-115, 117, 118, 121, 122, 127, and 133.
10 - 18 . (canceled)
19 . A pharmaceutical composition, comprising an antisense oligomer conjugate of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
20 . A method for treating Duchenne muscular dystrophy (DMD) in a subject in need thereof wherein the subject has a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the antisense oligomer conjugate of claim 1 .
21 . A method of restoring an mRNA reading frame to induce dystrophin production in a subject having a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the antisense oligomer conjugate of claim 1 .
22 . A method for treating Duchenne muscular dystrophy (DMD) in a subject in need thereof wherein the subject has a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the pharmaceutical composition of claim 19 .
23 . A method of restoring an mRNA reading frame to induce dystrophin production in a subject having a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the pharmaceutical composition of claim 19 .
24 . A method of excluding exon 53 from dystrophin pre-mRNA during mRNA processing in a subject having a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the pharmaceutical composition of claim 19 .
25 . A method of binding exon 53 of dystrophin pre-mRNA in a subject having a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the pharmaceutical composition of claim 19 .
26 . A pharmaceutical composition, comprising an antisense oligomer conjugate of claim 6 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
27 . A method for treating Duchenne muscular dystrophy (DMD) in a subject in need thereof wherein the subject has a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the antisense oligomer conjugate of claim 6 .
28 . A method of restoring an mRNA reading frame to induce dystrophin production in a subject having a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the antisense oligomer conjugate of claim 6 .
29 . A method for treating Duchenne muscular dystrophy (DMD) in a subject in need thereof wherein the subject has a mutation of the dystrophin gene that is amenable to exon 53 skipping, the method comprising administering to the subject the pharmaceutical composition of claim 26 .