JP2012525128A5 - - Google Patents

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JP2012525128A5
JP2012525128A5 JP2012507695A JP2012507695A JP2012525128A5 JP 2012525128 A5 JP2012525128 A5 JP 2012525128A5 JP 2012507695 A JP2012507695 A JP 2012507695A JP 2012507695 A JP2012507695 A JP 2012507695A JP 2012525128 A5 JP2012525128 A5 JP 2012525128A5
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antibody
seq
igf
antigen
binding fragment
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JP2012525128A (ja
JP5766179B2 (ja
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Priority claimed from PCT/EP2010/055458 external-priority patent/WO2010125003A1/en
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Claims (23)

  1. 配列番号:9のアミノ酸配列を含む重鎖可変領域CDR1;
    配列番号:23のアミノ酸配列を含む重鎖可変領域CDR2;
    配列番号:37のアミノ酸配列を含む重鎖可変領域CDR3;
    配列番号:51のアミノ酸配列を含む軽鎖可変領域CDR1;
    配列番号:65のアミノ酸配列を含む軽鎖可変領域CDR2;および
    配列番号:79のアミノ酸配列を含む軽鎖可変領域CDR3を含む、
    抗ActRIIB抗体またはそれらの抗原結合断片
  2. 配列番号:93の可変軽鎖配列および配列番号:107の可変重鎖
    含む、ActRIIB結合抗体またはそれらの抗原結合断片
  3. (a)配列番号:146の重鎖配列および配列番号:141の軽鎖配列;または
    (b)配列番号:156の重鎖配列および配列番号:151の軽鎖配列
    を含む、ActRIIB結合抗体またはそれらの抗原結合断片
  4. 前記抗体が、IgG1アイソタイプである、請求項1〜3のいずれかに記載の抗ActRIIB抗体またはそれらの抗原結合断片
  5. Fc領域の変異を介して改変されたエフェクター機能を有する、請求項1〜4のいずれかに記載の抗ActRIIB抗体。
  6. 請求項1〜5のいずれかに記載の抗体またはそれらの抗原結合断片をコードする単離されたポリヌクレオチド配列。
  7. 配列番号:121、135、141、146、151、156、161、166、171、または176の1つまたはそれ以上を含む、請求項に記載の単離されたポリヌクレオチド配列。
  8. 1つまたはそれ以上の請求項または請求項に記載の単離されたポリヌクレオチド配列を含むクローニングまたは発現ベクター。
  9. 請求項に記載の1つまたはそれ以上のベクターを含む、単離された宿主細胞。
  10. 請求項1−のいずれかに記載の抗体またはそれらの抗原結合断片の生産のための方法であって、請求項に記載の宿主細胞を培養し、該抗体またはそれらの抗原結合断片を単離することを含む方法。
  11. 請求項1−のいずれかに記載の抗体またはそれらの抗原結合断片または請求項または請求項7に記載のポリヌクレオチド配列を含む医薬組成物。
  12. 薬学的に許容される希釈剤または担体をさらに含む、請求項11に記載の医薬組成物。
  13. 1つまたはそれ以上のさらなる活性剤をさらに含む、請求項11または12に記載の医薬組成物。
  14. 前記さらなる活性剤がIGF−1、IGF−2またはIGF−1もしくはIGF−2の変異体、抗ミオスタチン抗体、ミオスタチンプロペプチド、ActRIIBに結合するが、それを活性化しないミオスタチンデコイタンパク質、ベータ2アゴニスト、Ghrelinアゴニスト、SARM、GHアゴニスト/模擬物またはフォリスタチンから選択される請求項13に記載の医薬組成物。
  15. 医薬として使用するための、請求項1−のいずれかに記載の抗体またはそれらの抗原結合断片、請求項または請求項に記載のポリヌクレオチド配列、または請求項1114のいずれかに記載の医薬組成物。
  16. 筋骨格疾患または障害の処置のための医薬の製造における、請求項1−のいずれかに記載の抗体またはそれらの抗原結合断片、請求項または請求項に記載のポリヌクレオチド配列、または請求項1114のいずれかに記載の医薬組成物の使用。
  17. 筋骨格疾患または障害の処置における使用のための、請求項1−のいずれかに記載の抗体またはそれらの抗原結合断片、請求項または請求項に記載のポリヌクレオチド配列、または請求項1114のいずれかに記載の医薬組成物。
  18. 前記筋骨格疾患または障害が、筋萎縮である、請求項16または17に記載の使用。
  19. 処置される患者が、IGF−1、IGF−2またはIGF−1もしくはIGF−2の変異体、抗ミオスタチン抗体、ミオスタチンプロペプチド、ActRIIBに結合するが、それを活性化しないミオスタチンデコイタンパク質、ベータ2アゴニスト、Ghrelinアゴニスト、SARM、GHアゴニスト/模擬物またはフォリスタチンで以前に処置されている、請求項18に記載の使用。
  20. 処置される患者が、IGF−1、IGF−2またはIGF−1もしくはIGF−2の変異体、抗ミオスタチン抗体、ミオスタチンプロペプチド、ActRIIBに結合するが、それを活性化しないミオスタチンデコイタンパク質、ベータ2アゴニスト、Ghrelinアゴニスト、SARM、GHアゴニスト/模擬物またはフォリスタチンでの処置に対して以前に屈折性であった、請求項18に記載の使用。
  21. 処置される患者が、高齢者であるか、無重力状態で過ごしているか、または不活化の期間を経験している、請求項18に記載の使用。
  22. 強化された不活化の期間または無重力状態の時間の前に、有効用量の請求項1−のいずれかの抗体またはそれらの抗原結合断片を投与することを含む、強化された不活化または無重力状態の時間の筋肉疲労効果を改善する方法。
  23. BW524(DSM2287)によってコードされるActRIIB抗体。
JP2012507695A 2009-04-27 2010-04-23 筋肉増殖を増加させるための組成物および方法 Active JP5766179B2 (ja)

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US17300409P 2009-04-27 2009-04-27
US61/173,004 2009-04-27
US30613710P 2010-02-19 2010-02-19
US61/306,137 2010-02-19
PCT/EP2010/055458 WO2010125003A1 (en) 2009-04-27 2010-04-23 Compositions and methods for increasing muscle growth

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JP2012525128A5 true JP2012525128A5 (ja) 2014-05-08
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EP (2) EP2424895B1 (ja)
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KR (1) KR101836501B1 (ja)
CN (2) CN102753578B (ja)
AR (1) AR076402A1 (ja)
AU (1) AU2010243697B2 (ja)
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CA (2) CA2993053A1 (ja)
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