IP Library Granted Patent US 10,329,319
Granted Patent B2
US 10,329,319 · App. 15/619,996 · Granted Jun 25, 2019

Antisense nucleic acids

Inventors: Naoki Watanabe (Tsukuba, JP); Youhei Satou (Tsukuba, JP); Shin'ichi Takeda (Kodaira, JP); Tetsuya Nagata (Kodaira, JP)
Assignees: NIPPON SHINYAKU CO., LTD.; NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY
C07H21/04C07H21/00C12N15/111C12N15/113C12N2310/11C12N2310/315C12N2310/3145C12N2310/321C12N2310/3525C12N2320/33
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Quick Facts
Patent No.
US 10,329,319
App. No.
15/619,996
Granted
Jun 25, 2019
Kind
B2
Abstract

The present invention provides an oligomer which efficiently enables to cause skipping of the 53rd exon in the human dystrophin gene. Also provided is a pharmaceutical composition which causes skipping of the 53rd exon in the human dystrophin gene with a high efficiency.

Claims (10)

1. An antisense oligomer consisting of any one nucleotide sequence selected from the group consisting of SEQ ID NOS: 8, 15, 32, 34, and 36, or pharmaceutically acceptable salt or hydrate thereof,

wherein the antisense oligomer is a morpholino oligomer, a peptide nucleic acid (PNA), or an oligonucleotide comprising at least one nucleotide having:

(i) a modified sugar moiety, wherein the 2′—OH group of a ribose is replaced by any one selected from the group consisting of 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), or

(ii) a modified phosphate-binding region selected from the group consisting of a phosphorothioate bond, a phosphorodithioate bond, an alkylphosphonate bond, a phosphoramidate bond, and a boranophosphate bond.

2. The antisense oligomer according to claim 1 , or pharmaceutically acceptable salt or hydrate thereof, wherein the antisense oligomer is an oligonucleotide.

3. The antisense oligomer according to claim 1 , or pharmaceutically acceptable salt or hydrate thereof, wherein the antisense oligomer is a morpholino oligomer.

4. The antisense oligomer according to claim 3 , or pharmaceutically acceptable salt or hydrate thereof, wherein the antisense oligomer is a phosphorodiamidate morpholino oligomer.

5. The antisense oligomer according to claim 3 , or pharmaceutically acceptable salt or hydrate thereof, wherein the 5′ end of the antisense oligomer is any one of the groups of chemical formulae (1) to (3) below:

6. 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.

7. The pharmaceutical composition for the treatment of muscular dystrophy of claim 6 , which is administered for the treatment of Duchenne muscular dystrophy.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2017
From: WATANABE, NAOKI; SATOU, YOUHEI; TAKEDA, SHIN'ICHI; NAGATA, TETSUYA
To: NIPPON SHINYAKU CO., LTD.; NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY
Reel/Frame 042677/0613 →
Priority Claims (1)
JP 2010-196032 · Sep 1, 2010 · national
Continuity (3)
Continuation 14615504 · Feb 6, 2015
Continuation 13819520
Related Publication 20170320903A1 · Nov 9, 2017
Cited By (13)
US 12,239,716 US 12,239,717 US 12,263,225 US 12,325,753 US 12,329,824 US 12,329,825 US 12,357,703 US 12,397,062 US 12,403,203 US 12,428,487 US 12,440,575 US 12,478,687 US 12,662,545