JP2015533141A5 - - Google Patents

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JP2015533141A5
JP2015533141A5 JP2015536139A JP2015536139A JP2015533141A5 JP 2015533141 A5 JP2015533141 A5 JP 2015533141A5 JP 2015536139 A JP2015536139 A JP 2015536139A JP 2015536139 A JP2015536139 A JP 2015536139A JP 2015533141 A5 JP2015533141 A5 JP 2015533141A5
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Claims (17)

  1. 以下の式A:
    Figure 2015533141
    式B:
    Figure 2015533141
    および式C:
    Figure 2015533141
    から選択される化合物、ならびにその塩および溶媒和物。
  2. 以下の式ConjA:
    Figure 2015533141
    式ConjB:
    Figure 2015533141
    または式ConjC:
    Figure 2015533141
    (上記の式中、CBAは細胞結合剤を表す)
    である複合体。
  3. 前記細胞結合剤は、抗体またはその活性断片である、請求項2に記載の複合体。
  4. 前記抗体または抗体断片は、腫瘍関連抗原の抗体または抗体断片である、請求項3に記載の複合体。
  5. 前記抗体または抗体断片は、以下の(1)〜(88)から選択される1種または複数の腫瘍関連抗原または細胞表面受容体に結合する抗体である、請求項3に記載の複合体:
    (1)BMPR1B;
    (2)E16;
    (3)STEAP1;
    (4)0772P;
    (5)MPF;
    (6)Napi3b;
    (7)Sema 5b;
    (8)PSCA hlg;
    (9)ETBR;
    (10)MSG783;
    (11)STEAP2;
    (12)TrpM4;
    (13)CRIPTO;
    (14)CD21;
    (15)CD79b;
    (16)FcRH2;
    (17)HER2;
    (18)NCA;
    (19)MDP;
    (20)IL20R−α;
    (21)ブレビカン;
    (22)EphB2R;
    (23)ASLG659;
    (24)PSCA;
    (25)GEDA;
    (26)BAFF−R;
    (27)CD22;
    (28)CD79a;
    (29)CXCR5;
    (30)HLA−DOB;
    (31)P2X5;
    (32)CD72;
    (33)LY64;
    (34)FcRH1;
    (35)IRTA2;
    (36)TENB2;
    (37)PSMA−FOLH1;
    (38)SST;
    (38.1)SSTR2;
    (38.2)SSTR5;
    (38.3)SSTR1;
    (38.4)SSTR3;
    (38.5)SSTR4;
    (39)ITGAV;
    (40)ITGB6;
    (41)CEACAM5;
    (42)MET;
    (43)MUC1;
    (44)CA9;
    (45)EGFRvIII;
    (46)CD33;
    (47)CD19;
    (48)IL2RA;
    (49)AXL;
    (50)CD30−TNFRSF8;
    (51)BCMA−TNFRSF17;
    (52)CT Ags−CTA;
    (53)CD174(ルイス式Y)−FUT3;
    (54)CLEC14A;
    (55)GRP78−HSPA5;
    (56)CD70;
    (57)幹細胞特異的抗原;
    (58)ASG−5;
    (59)ENPP3;
    (60)PRR4;
    (61)GCC−GUCY2C;
    (62)Liv−1−SLC39A6;
    (63)5T4;
    (64)CD56−NCMA1;
    (65)CanAg;
    (66)FOLR1;
    (67)GPNMB;
    (68)TIM−1−HAVCR1;
    (69)RG−1/前立腺腫瘍標的ミンディン−ミンディン/RG−1;
    (70)B7−H4−VTCN1;
    (71)PTK7;
    (72)CD37;
    (73)CD138−SDC1;
    (74)CD74;
    (75)クローディン−CL;
    (76)EGFR;
    (77)Her3;
    (78)RON−MST1R;
    (79)EPHA2;
    (80)CD20−MS4A1;
    (81)テネイシンC−TNC;
    (82)FAP;
    (83)DKK−1;
    (84)CD52;
    (85)CS1−SLAMF7;
    (86)エンドグリン−ENG;
    (87)アネキシンA1−ANXA1;
    (88)V−CAM(CD106)−VCAM1。
  6. 前記抗体または抗体断片は、システイン操作した抗体である、請求項2から5のいずれか1項に記載の複合体。
  7. 抗体(Ab)に対する薬物(D)の薬物積載量(p)は、1〜約8の整数である、請求項2から6のいずれか1項に記載の複合体。
  8. pは、1、2、3、または4である、請求項7に記載の複合体。
  9. 請求項2から8のいずれか1項に記載の薬物複合体化合物の混合物を含む組成物であって、抗体薬物複合体化合物の該混合物中の抗体あたりの前記薬物積載量の平均は約1〜約8である、組成物。
  10. 治療に用いるための、請求項2から8のいずれか1項に記載の複合体または請求項9に記載の組成物。
  11. 治療対象の増殖性疾患を治療するのに用いるための、請求項2から8のいずれか1項に記載の複合体または請求項9に記載の組成物。
  12. 前記疾患は癌である、請求項11に記載の複合体または組成物。
  13. 請求項2から8のいずれか1項に記載の複合体または請求項9に記載の組成物、および薬学的に許容可能な希釈剤、キャリア、または賦形剤を含む、医薬組成物。
  14. 治療上有効量の化学療法薬をさらに含む、請求項13に記載の医薬組成物。
  15. 治療対象における増殖性疾患を治療するために用いる医薬の調製における、請求項2から8のいずれか1項に記載の複合体または請求項9に記載の組成物の使用。
  16. 求項14に記載の医薬組成物を含む、癌治療剤
  17. 請求項2から8のいずれか1項に記載の複合体を調製する方法であって、細胞結合剤を、請求項1に定義されるとおりの化合物A、B、またはCと反応させる工程を含む、方法。
JP2015536139A 2012-10-12 2013-10-11 ピロロベンゾジアゼピン類およびその複合体 Active JP6367811B2 (ja)

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US201261712924P 2012-10-12 2012-10-12
US61/712,924 2012-10-12
PCT/EP2013/071235 WO2014057073A1 (en) 2012-10-12 2013-10-11 Pyrrolobenzodiazepines and conjugates thereof

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KR (3) KR20200003278A (ja)
CN (2) CN110256469B (ja)
AU (1) AU2013328674B2 (ja)
BR (1) BR112015008251B1 (ja)
CA (2) CA2885315C (ja)
CY (2) CY1121390T1 (ja)
DK (2) DK2906248T3 (ja)
ES (2) ES2847050T3 (ja)
HK (1) HK1213183A1 (ja)
HR (2) HRP20190366T1 (ja)
HU (2) HUE043738T4 (ja)
LT (2) LT2906248T (ja)
MX (2) MX362004B (ja)
NZ (2) NZ745069A (ja)
PL (2) PL2906248T3 (ja)
PT (2) PT2906248T (ja)
RS (2) RS58203B1 (ja)
SI (2) SI2906248T1 (ja)
TR (1) TR201902494T4 (ja)
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