IP Library Granted Patent US 12,064,483
Granted Patent B2
US 12,064,483 · App. 17/843,705 · Granted Aug 20, 2024

Nucleic acid-polypeptide compositions and methods of inducing exon skipping

Inventors: Arthur A. Levin (Del Mar, CA); Andrew John Geall (Carlsbad, CA); Venkata Ramana Doppalapudi (San Diego, CA); Michael Caramian Cochran (La Jolla, CA); Hanhua Huang (San Diego, CA); Rob Burke (Encinitas, CA)
Assignee: AVIDITY BIOSCIENCES, INC.
A61K47/6803A61K31/7088A61K31/713A61K47/60A61K47/6455A61K47/6807A61K47/6849A61K48/0058A61K48/0066A61K48/0083A61P21/00C07K14/003C07K16/2881C07K16/40C12N15/113A61K38/00C12N2310/11C12N2310/315C12N2310/3233C12N2310/3513C12N2320/32C12N2320/33
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Quick Facts
Patent No.
US 12,064,483
App. No.
17/843,705
Filed
Jun 17, 2022
Granted
Aug 20, 2024
Kind
B2
Art Unit
1635
USPC
514/44A
Abstract

Disclosed herein are molecules and pharmaceutical compositions that induce an insertion, deletion, duplication, or alteration in an incorrectly spliced mRNA transcript to induce exon skipping or exon inclusion. Also described herein include methods for treating a disease or disorder that comprises a molecule or a pharmaceutical composition that induces an insertion, deletion, duplication, or alteration in an incorrectly spliced mRNA transcript to induce exon skipping or exon inclusion.

Claims (26)

1. A method of treating muscular dystrophy in a subject in need thereof, comprising:

administering to the subject a single stranded oligonucleotide conjugate comprising an anti-transferrin receptor antibody or antigen binding fragment thereof conjugated to a single stranded oligonucleotide hybridizing to an acceptor splice site, a donor splice site, or an exonic splice enhancer element of a pre-mRNA transcript of the DMD gene;

wherein the single stranded oligonucleotide induces exon skipping in said pre-mRNA transcript to generate an mRNA transcript encoding a truncated dystrophin protein, thereby treating the muscular dystrophy in the subject.

2. The method of claim 1 , wherein the single stranded oligonucleotide is a phosphorodiamidate morpholino oligonucleotide (PMO) or an antisense oligonucleotide (ASO).

3. The method of claim 1 , wherein the single stranded oligonucleotide is delivered into a muscle cell.

4. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 8 of the DMD gene.

5. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 23 of the DMD gene.

6. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 35 of the DMD gene.

7. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 43 of the DMD gene.

8. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 44 of the DMD gene.

9. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 45 of the DMD gene.

10. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 50 of the DMD gene.

11. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 51 of the DMD gene.

12. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 52 of the DMD gene.

13. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 53 of the DMD gene.

14. The method of claim 1 , wherein the single stranded oligonucleotide induces skipping of exon 55 of the DMD gene.

15. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises a monoclonal antibody or antigen binding fragment thereof or a monovalent Fab′.

16. The method of claim 1 , wherein the single stranded oligonucleotide comprises at least from about 10 to about 30 nucleotides in length.

17. The method of claim 1 , wherein the single stranded oligonucleotide is conjugated to the antibody or antigen binding fragment thereof via a linker.

18. The method of claim 17 , wherein the linker is a cleavable linker.

19. The method of claim 17 , wherein the linker is a non-cleavable linker.

20. The method of claim 17 , wherein the linker is selected from the group consisting of a heterobifunctional linker, a homobifunctional linker, a maleimide group, a dipeptide moiety, a benzoic acid group or derivatives thereof, a C 1 -C 6 alkyl group, and a combination thereof.

21. The method of claim 1 , wherein the single stranded oligonucleotide conjugate has a single stranded oligonucleotide to antibody ratio of about 1:1, 2:1, 3:1, or 4:1.

22. The method of claim 1 , wherein the single stranded oligonucleotide conjugate is formulated for parenteral administration.

23. The method of claim 1 , wherein the truncated dystrophin protein modulates muscular dystrophy.

24. The single stranded oligonucleotide of claim 23 , wherein the muscular dystrophy is Duchenne muscular dystrophy or Becker muscular dystrophy.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2022
From: LEVIN, ARTHUR A.; GEALL, ANDREW JOHN; DOPPALAPUDI, VENKATA RAMANA; COCHRAN, MICHAEL CARAMIAN; HUANG, HANHUA; BURKE, ROB
To: AVIDITY BIOSCIENCES LLC
Reel/Frame 061374/0098 →
CHANGE OF NAME Recorded Oct 11, 2022
From: AVIDITY BIOSCIENCES LLC
To: AVIDITY BIOSCIENCES, INC.
Reel/Frame 061639/0584 →
Continuity (7)
Continuation 17463484 · Aug 31, 2021
Continuation 16129696 · Sep 12, 2018
Continuation 16128450 · Sep 11, 2018
Continuation PCTUS2018012672 · Jan 5, 2018
Provisional Application 62561939 · Sep 22, 2017
Provisional Application 62443514 · Jan 6, 2017
Related Publication 20220313833A1 · Oct 6, 2022
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