JP2020510039A5 - - Google Patents

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JP2020510039A5
JP2020510039A5 JP2019548920A JP2019548920A JP2020510039A5 JP 2020510039 A5 JP2020510039 A5 JP 2020510039A5 JP 2019548920 A JP2019548920 A JP 2019548920A JP 2019548920 A JP2019548920 A JP 2019548920A JP 2020510039 A5 JP2020510039 A5 JP 2020510039A5
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antibody
pharmaceutical combination
chain variable
variable region
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Claims (21)

  1. 以下を含む、医薬組合せ:
    (A)配列番号1に示されるアミノ酸配列を含む重鎖可変領域および配列番号2に示されるアミノ酸配列を含む軽鎖可変領域を含む抗体とLY75への結合をめぐって競合する抗LY75抗体、またはその抗原結合部分;
    あるいは
    以下を含む抗LY75抗体、またはその抗原結合部分:
    a)以下を含む、重鎖可変領域:
    i)配列番号5を含む第1のvhCDRと;
    ii)配列番号6を含む第2のvhCDRと;
    iii)配列番号7を含む第3のvhCDR;および
    b)以下を含む、軽鎖可変領域:
    i)配列番号8を含む第1のvlCDRと;
    ii)配列番号9を含む第2のvlCDRと;
    iii)配列番号10を含む第3のvlCDR;
    (任意に、上記配列番号のいずれか1つもしくは複数は、独立して1、2、3、4もしくは5つのアミノ酸置換、付加または欠失を含む);
    ならびに
    (B)以下を含む、抗CD20抗体、もしくはその抗原結合部分:
    a)以下を含む、重鎖可変領域:
    i)配列番号40を含む第1のvhCDRと;
    ii)配列番号41を含む第2のvhCDRと;
    iii)配列番号42を含む第3のvhCDR;および
    b)以下を含む、軽鎖可変領域:
    i)配列番号43を含む第1のvlCDRと;
    ii)配列番号44を含む第2のvlCDRと;
    iii)配列番号45を含む第3のvlCDR;
    (任意に、上記配列番号のいずれか1つもしくは複数は、独立して1、2、3、4もしくは5つのアミノ酸置換、付加または欠失を含む);

    (ここで、前記医薬組合せは、同時、個別または逐次使用のための、組合せ製剤の形態である)。
  2. 以下を含む、医薬組合せ:
    (A)配列番号1に示されるアミノ酸配列を含む重鎖可変領域および配列番号2に示されるアミノ酸配列を含む軽鎖可変領域を含む抗体とLY75への結合をめぐって競合する抗LY75抗体、またはその抗原結合部分;
    あるいは
    以下を含む抗LY75抗体、またはその抗原結合部分:
    a)以下を含む、重鎖可変領域:
    i)配列番号5を含む第1のvhCDRと;
    ii)配列番号6を含む第2のvhCDRと;
    iii)配列番号7を含む第3のvhCDR;および
    b)以下を含む、軽鎖可変領域:
    i)配列番号8を含む第1のvlCDRと;
    ii)配列番号9を含む第2のvlCDRと;
    iii)配列番号10を含む第3のvlCDR;
    (任意に、上記配列番号のいずれか1つもしくは複数は、独立して1、2、3、4もしくは5つのアミノ酸置換、付加または欠失を含む);
    ならびに
    (B)イブルチニブまたはその薬学的に許容される塩
    (ここで、前記医薬組合せは、同時、個別または逐次使用のための、組合せ製剤の形態である)。
  3. 配列番号5〜10のいずれか1つまたは複数が、独立して1、2、3、4または5つの保存的アミノ酸置換を含む、請求項1または請求項2に記載の医薬組合せ。
  4. 前記抗LY75抗体またはその抗原結合部分が、配列番号1と少なくとも80%、85%、90%、95%、99%または100%のアミノ酸配列同一性を有する重鎖可変領域、および配列番号2と少なくとも80%、85%、90%、95%、99%または100%のアミノ酸配列同一性を有する軽鎖可変領域を含む、請求項1〜のいずれか一項に記載の医薬組合せ。
  5. 前記抗LY75抗体がヒトIgG1モノクローナル抗体である、請求項1〜のいずれか一項に記載の医薬組合せ。
  6. 前記抗LY75抗体またはその抗原結合部分が、共有結合した部位をさらに含む、請求項1〜のいずれか一項に記載の医薬組合せ。
  7. 前記部位が薬物である、請求項6に記載の医薬組合せ。
  8. 前記薬物がメイタンシノイドまたはその誘導体である、請求項に記載の医薬組合せ。
  9. 前記薬物がDM4またはDM1である、請求項に記載の医薬組合せ。
  10. 配列番号40〜45のいずれか1つまたは複数が、独立して1、2、3、4または5つの保存的アミノ酸置換を含む、請求項1または3〜のいずれか一項に記載の医薬組合せ。
  11. 前記抗CD20抗体が、マウス/ヒトキメラ抗体、ヒト化抗体またはヒト抗体である、請求項1または3〜10のいずれか一項に記載の医薬組合せ。
  12. 前記抗CD20抗体がリツキシマブである、請求項1または3〜11のいずれか一項に記載の医薬組合せ。
  13. (A)および/または(B)が、1つもしくは複数の薬学的に許容される希釈剤、賦形剤または担体をさらに含む、請求項1〜12のいずれか一項に記載の医薬組合せ。
  14. 前記医薬組合せが、びまん性大細胞型B細胞リンパ腫(DLBCL)または非ホジキンリンパ腫の治療における同時、個別もしくは逐次使用のための組合せ製剤の形態である、請求項1〜13のいずれか一項に記載の医薬組合せ。
  15. がんの治療への使用のための請求項1〜13のいずれか一項に記載の医薬組合せであって、成分(A)および(B)が、前記がんの治療のために前記患者に同時に、個別にまたは逐次的に投与される医薬組合せ。
  16. 前記抗LY75抗体またはその抗原結合部分が、LY75を発現する細胞に取り込まれる、請求項15に記載の使用のための医薬組合せ。
  17. 前記抗LY75抗体または抗原結合部分が、共有結合した薬物を含む、請求項15または16に記載の使用のための医薬組合せ。
  18. 前記共有結合した薬物がメイタンシノイドである、請求項17に記載の使用のための医薬組合せ。
  19. 前記メイタンシノイドがDM4である、請求項18に記載の使用のための医薬組合せ。
  20. 前記がんがびまん性大細胞型B細胞リンパ腫(DLBCL)または非ホジキンリンパ腫である、請求項15〜19のいずれか一項に記載の使用のための医薬組合せ。
  21. 治療における使用のための、または薬剤としての使用のための、請求項1〜14のいずれか一項に記載の医薬組合せ。
JP2019548920A 2017-03-10 2018-03-09 抗ly75抗体を含む医薬組合せ Active JP7220153B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1703876.1A GB201703876D0 (en) 2017-03-10 2017-03-10 Pharmaceutical combinations
GB1703876.1 2017-03-10
PCT/EP2018/055939 WO2018162727A1 (en) 2017-03-10 2018-03-09 Pharmaceutical combinations comprising an anti-ly75 antibody

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JP2020510039A JP2020510039A (ja) 2020-04-02
JP2020510039A5 true JP2020510039A5 (ja) 2021-04-08
JP7220153B2 JP7220153B2 (ja) 2023-02-09

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US (2) US11365258B2 (ja)
EP (2) EP4257614A3 (ja)
JP (1) JP7220153B2 (ja)
KR (1) KR102538294B1 (ja)
CN (2) CN116808198A (ja)
AR (1) AR111265A1 (ja)
AU (2) AU2018232886B2 (ja)
CA (1) CA3054904A1 (ja)
CO (1) CO2019009815A2 (ja)
CR (1) CR20190422A (ja)
EA (1) EA201991845A1 (ja)
GB (1) GB201703876D0 (ja)
IL (1) IL269140A (ja)
MA (1) MA49977A (ja)
MX (2) MX2019010673A (ja)
MY (1) MY197735A (ja)
PH (1) PH12019502000A1 (ja)
SG (1) SG11201907207UA (ja)
TW (2) TWI789379B (ja)
UA (1) UA128081C2 (ja)
UY (1) UY37630A (ja)
WO (1) WO2018162727A1 (ja)
ZA (2) ZA201905021B (ja)

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