IP Library Granted Patent US 10,994,020
Granted Patent B2
US 10,994,020 · App. 16/128,450 · Granted May 4, 2021

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 10,994,020
App. No.
16/128,450
Granted
May 4, 2021
Kind
B2
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 (28)

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

administering to the subject a phosphorodiamidate morpholino oligonucleotide (PMO) conjugate to deliver the PMO conjugate preferentially into a muscle cell, wherein the PMO conjugate is a PMO conjugated to an anti-transferrin receptor antibody, wherein the anti-transferrin receptor antibody comprises two light chain variable domains and two heavy chain variable domains;

wherein the PMO targets an acceptor splice site, a donor splice site, or an exonic splice enhancer element of a pre-mRNA of the DMD gene;

wherein the PMO conjugate induces splicing out of an exon to generate a mRNA transcript; and wherein the mRNA transcript encodes a truncated dystrophin protein,

thereby treating the Duchenne muscular dystrophy in the subject.

2. The method of claim 1 , wherein the splicing event is of exon 8 of DMD gene.

3. The method of claim 1 , wherein the splicing event is of exon 44.

4. The method of claim 1 , wherein the splicing event is of exon 45.

5. The method of claim 1 , wherein the anti-transferrin receptor antibody comprises a humanized antibody, chimeric antibody, monoclonal antibody, divalent Fab2, diabody, or minibody.

6. The method of claim 1 , wherein the PMO is an antisense oligonucleotide.

7. The method of claim 1 , wherein the PMO comprises at least from about 10 to about 30 nucleotides in length.

8. The method of claim 1 , wherein the PMO comprises a sequence that hybridizes to a portion of exon 51 of DMD gene.

9. The method of claim 1 , wherein the PMO comprises a sequence that hybridizes to a portion of exon 44 of DMD gene.

10. The method of claim 1 , wherein the PMO is conjugated to the anti-transferrin receptor antibody via a linker.

11. The method of claim 10 , wherein the linker is a cleavable linker.

12. The method of claim 10 , wherein the linker is a non-cleavable linker.

13. The method of claim 10 , 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, or a combination thereof.

14. The method of claim 1 , wherein the PMO conjugate has a PMO to antibody ratio of about 1:1, 2:1, 3:1, or 4:1.

15. The method of claim 1 , wherein the subject is a human.

16. The method of claim 1 , wherein the PMO comprises at least 90%, 95%, 99%, or 100% sequence identity to a sequence that 17 hybridizes to SEQ ID NO: 59.

17. The method of claim 1 , wherein the splicing event is of exon 23 of DMD gene.

18. The method of claim 1 , wherein the splicing event is of exon 35 of DMD gene.

19. The method of claim 1 , wherein the splicing event is of exon 43 of DMD gene.

20. The method of claim 1 , wherein the splicing event is of exon 50 of DMD gene.

21. The method of claim 1 , wherein the splicing event is of exon 51 of DMD gene.

22. The method of claim 1 , wherein the splicing event is of exon 52 of DMD gene.

23. The method of claim 1 , wherein the splicing event is of exon 53 of DMD gene.

24. The method of claim 1 , wherein the splicing event is of exon 55 of DMD gene.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY PREVIOUSLY RECORDED AT REEL: 050018 FRAME: 0456. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Sep 12, 2019
From: AVIDITY BIOSCIENCES LLC
To: AVIDITY BIOSCIENCES, INC.
Reel/Frame 050371/0483 →
CHANGE OF NAME Recorded Aug 9, 2019
From: AVIDITY BIOSCIENCES LLC
To: AVIDITY BIOSCIENCES LLC; AVIDITY BIOSCIENCES, INC.
Reel/Frame 050018/0456 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 25, 2018
From: LEVIN, ARTHUR A.; GEALL, ANDREW JOHN; DOPPALAPUDI, VENKATA RAMANA; COCHRAN, MICHAEL CARAMIAN; HUANG, HANHUA; BURKE, ROB
To: AVIDITY BIOSCIENCES LLC
Reel/Frame 047315/0356 →
Continuity (4)
Continuation PCTUS2018012672 · Jan 5, 2018
Provisional Application 62561939 · Sep 22, 2017
Provisional Application 62443514 · Jan 6, 2017
Related Publication 20180369400A1 · Dec 27, 2018
Cited By (25)
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