IP Library › Granted Patent US 9,890,381
Granted Patent B2
US 9,890,381 · App. 15/339,069 · Granted Feb 13, 2018

Antisense nucleic acids

Inventors: Naoki Watanabe (Ibaraki, JP); Haruna Seo (Tokyo, JP); Shin'ichi Takeda (Tokyo, JP); Tetsuya Nagata (Tokyo, JP)
Assignees: NIPPON SHINYAKU CO., LTD.; NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY
C12N15/113C12N15/111C12N2310/11C12N2310/314C12N2310/315C12N2310/321C12N2310/322C12N2310/3233C12N2320/33
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,890,381
App. No.
15/339,069
Granted
Feb 13, 2018
Kind
B2
Abstract

The present invention provides a pharmaceutical agent which causes skipping of the 55th, 45th, 50th or 44th exon in the human dystrophin gene with a high efficiency. The present invention provides an oligomer which efficiently enables to cause skipping of the 55th, 45th, 50th or 44th exon in the human dystrophin gene.

Claims (9)

1. An antisense oligomer which causes skipping of the 55th exon in a human dystrophin gene, wherein the base sequence of the antisense oligomer consists of the base sequence of (i) the 157th to the 177th nucleotides of SEQ ID NO: 5, or (ii) the 157th to the 176th nucleotides of SEQ ID NO: 5, and wherein the antisense oligomer is a morpholino oligomer, or an oligonucleotide in which the sugar moiety and/or the phosphate-binding region of at least one nucleotide constituting the oligonucleotide is modified.

2. The antisense oligomer according to claim 1 , wherein the sugar moiety of at least one nucleotide constituting the oligonucleotide is a ribose in which the 2′-OH group is replaced by any one selected from the group consisting of OR, R, R′OR, SH, SR, NH 2 , NHR, NR 2 , N 3 , CN, F, Cl, Br and I (wherein R is an alkyl or an aryl and R′ is an alkylene).

3. The antisense oligomer according to claim 1 , wherein the phosphate-binding region of at least one nucleotide constituting the oligonucleotide is any one selected from the group consisting of a phosphorothioate bond, a phosphorodithioate bond, an alkylphosphonate bond, a phosphoramidate bond and a boranophosphate bond.

4. The antisense oligomer according to claim 1 , which is a morpholino oligomer.

5. The antisense oligomer according to claim 4 , which is a phosphorodiamidate morpholino oligomer.

6. The antisense oligomer according to claim 4 , wherein the 5′ end of the morpholino oligomer is any one of the groups of chemical formulae (1) to (3) below:

7. A pharmaceutical composition for the treatment of muscular dystrophy, comprising as an active ingredient the antisense oligomer according to claim 1 , or a pharmaceutically acceptable salt or hydrate thereof.

8. A method of treating muscular dystrophy, comprising administering to a patient in need thereof a therapeutically effective amount of the antisense oligomer according to claim 1 .

9. A method of treating muscular dystrophy, comprising administering to a patient in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 7 .

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE CITY OF ASSIGNEE NIPPON SHINYAKU CO., LTD. FROM "KYOTO-SHI, KYOGO" TO --KYOTO-SHI, KYOTO PREVIOUSLY RECORDED AT REEL: 040177 FRAME: 0076. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Sep 22, 2020
From: WATANABE, NAOKI; SEO, HARUNA; TAKEDA, SHIN'ICHI; NAGATA, TETSUYA
To: NIPPON SHINYAKU CO., LTD.; NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY
Reel/Frame 053853/0467 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2016
From: WATANABE, NAOKI; SEO, HARUNA; TAKEDA, SHIN'ICHI; NAGATA, TETSUYA
To: NIPPON SHINYAKU CO., LTD.; NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY
Reel/Frame 040177/0076 →
Priority Claims (2)
JP 2011-288040 · Dec 28, 2011 · national
JP 2012-043092 · Feb 29, 2012 · national
Continuity (2)
Division 14368307
Related Publication 20170067052A1 · Mar 9, 2017