JP2020022483A5 - - Google Patents

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JP2020022483A5
JP2020022483A5 JP2019190648A JP2019190648A JP2020022483A5 JP 2020022483 A5 JP2020022483 A5 JP 2020022483A5 JP 2019190648 A JP2019190648 A JP 2019190648A JP 2019190648 A JP2019190648 A JP 2019190648A JP 2020022483 A5 JP2020022483 A5 JP 2020022483A5
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modified oligonucleotide
pharmaceutical composition
pharmaceutically acceptable
pbs
buffered saline
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JP2020022483A (ja
JP6924242B2 (ja
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  1. 以下の化学構造:
    Figure 2020022483
    (配列番号49)
    またはその塩に従う、修飾オリゴヌクレオチド。
  2. 以下の化学構造:
    Figure 2020022483
    (配列番号49)
    に従う、修飾オリゴヌクレオチド。
  3. ナトリウム塩又はカリウム塩である、請求項1に記載の修飾オリゴヌクレオチド。
  4. 請求項1〜3のいずれか1項に記載の修飾オリゴヌクレオチド、及び薬学的に許容される担体又は希釈剤を含む、医薬組成物。
  5. 薬学的に許容される希釈剤を含み、該薬学的に許容される希釈剤がリン酸緩衝生理食塩水(PBS)である、請求項4に記載の医薬組成物。
  6. 医薬組成物が、本質的に前記修飾オリゴヌクレオチド及びリン酸緩衝生理食塩水(PBS)からなる、請求項4に記載の医薬組成物。
  7. 修飾オリゴヌクレオチドを含む化合物であって、
    該修飾オリゴヌクレオチドが、5’ウイングセグメント、中央のギャップセグメント、及び3’ウイングセグメントからなるギャップマーであり、
    5’ウイングセグメントが、6個の2’−O−メトキシエチルヌクレオシドからなり、
    中央のギャップセグメントが、10個のβ−D−デオキシリボヌクレオシドからなり、
    3’ウイングセグメントが、4個の2’−O−メトキシエチルヌクレオシドからなり、
    該修飾オリゴヌクレオチドが核酸塩基配列5’−GGTTAATCTTTATCAGGTCT−3’(配列番号49)を有し、各シトシンが5−メチルシトシンであり、該修飾オリゴヌクレオチドのヌクレオシド間結合が、5’から3’に、sooooossssssssssossであり、ここで、各sはホスホロチオエート結合であり、各oはホスホジエステル結合である、上記化合物。
  8. 修飾オリゴヌクレオチドが共役基に共有結合している、請求項7に記載の化合物。
  9. 請求項7又は8に記載の化合物、及び薬学的に許容される担体又は希釈剤を含む、医薬組成物。
  10. 薬学的に許容される希釈剤を含み、該薬学的に許容される希釈剤がリン酸緩衝生理食塩水(PBS)である、請求項9に記載の医薬組成物。
  11. 医薬組成物が、本質的に前記修飾オリゴヌクレオチド及びリン酸緩衝生理食塩水(PBS)からなる、請求項9に記載の医薬組成物。
JP2019190648A 2015-04-16 2019-10-18 C9orf72発現を調節するための組成物 Active JP6924242B2 (ja)

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US201562148691P 2015-04-16 2015-04-16
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US201562239400P 2015-10-09 2015-10-09
US62/239,400 2015-10-09
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EP (2) EP3283080B1 (ja)
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KR (2) KR102258516B1 (ja)
CN (2) CN113265404A (ja)
AU (2) AU2016249002B2 (ja)
BR (1) BR112017016068A2 (ja)
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