[EN] EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY<br/>[FR] CONJUGUÉS OLIGOMÈRES DE SAUTS D'EXONS POUR LA DYSTROPHIE MUSCULAIRE
申请人:SAREPTA THERAPEUTICS INC
公开号:WO2018118662A1
公开(公告)日:2018-06-28
Antisense oligomer conjugates complementary to a selected target site in the human dystrophin gene to induce exon 53 skipping are described.
与人类肌营养不良基因中选择的靶位点互补的反义寡核苷酸共轭物用于诱导外显子53跳跃。
FATTY ACID ACETYLATED SALICYLATES AND THEIR USES
申请人:Milne Jill C.
公开号:US20100041748A1
公开(公告)日:2010-02-18
The invention relates to Fatty Acid Acetylated Salicylate Derivatives; compositions comprising an effective amount of a Fatty Acid Acetylated Salicylate Derivative; and methods for treating or preventing an inflammatory disorder comprising the administration of an effective amount of a Fatty Acid Acetylated Salicylate Derivative.
EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY
申请人:Sarepta Therapeutics, Inc.
公开号:US20180177814A1
公开(公告)日:2018-06-28
Antisense oligomer conjugates complementary to a selected target site in the human dystrophin gene to induce exon 51 skipping are described.
抗义核苷酸寡聚体结合到人类肌营养不良基因中的特定靶位点,诱导外显子51跳跃。
EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPY
申请人:Sarepta Therapeutics, Inc.
公开号:US20200190516A1
公开(公告)日:2020-06-18
Antisense oligomers complementary to a selected target site in the human dystrophin gene to induce exon 50 skipping are described. In various aspects, antisense oligomers are described according to Formula (I):
or a pharmaceutically acceptable salt thereof, wherein T, Nu, n, and R
100
are defined herein.
[EN] COMBINATION THERAPIES FOR TREATING MUSCULAR DYSTROPHY<br/>[FR] POLYTHÉRAPIES POUR TRAITER UNE DYSTROPHIE MUSCULAIRE
申请人:SAREPTA THERAPEUTICS INC
公开号:WO2019067979A1
公开(公告)日:2019-04-04
The present disclosure relates to methods of treating Duchenne's Muscular Dystrophy by administering an antisense oligonucleotide that induces exon skipping and a non-steroidal anti- inflammatory compound.