Methods for treatment of cancer with an anti-tigit antagonist antibody
US-2024424092-A1 · Dec 26, 2024 · US
US2018201678A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018201678-A1 |
| Application number | US-201615743764-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 15, 2016 |
| Priority date | Jul 16, 2015 |
| Publication date | Jul 19, 2018 |
| Grant date | — |
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The present disclosure relates to antibody molecules comprising a binding domain specific to CD79, said binding domain comprising SEQ ID NO: 1, 2, 3 or 4, and/or SEQ ID NO: 5, 6 and 7. The disclosure also extends to pharmaceutical compositions comprising said antibody molecules and use of the antibody molecules/compositions in treatment.
Opening claim text (preview).
1 . An antibody molecule comprising a binding domain specific to CD79 wherein the binding domain comprises a heavy chain variable domain (VH) comprising: CDRH1 of formula (I): (SEQ ID NO: 1) GFSLX 1 NYX 2 X 3 X 4 wherein X 1 is S or N, X 2 is V or A, X 3 is V or M and X 4 is S or V, CDRH2 of formula (II): (SEQ ID NO: 2) IIYX 5 X 6 X 7 X 8 X 9 X 10 X 11 YAX 12 WAKG wherein X 5 is V or I, X 6 is S or E, X 7 is T or G and X 8 is N or G, X 9 is T or A, X 10 is T or Y, X 11 is W or absent, X 12 is N or S, CDHR3 is (SEQ ID NO: 3) EPYEPYDDSNIYYGMDP or (SEQ ID NO: 4) DAGHSDVDVLDI, and a light chain variable domain (VL), wherein the light chain variable domain (VL) comprises: a CDRL1 of formula (III): (SEQ ID NO: 5) QX 13 SQSX 14 X 15 X 16 X 17 NX 18 LA wherein X 13 is A or S, X 14 is V or I, X 15 is V or Y and X 16 is N or S, X 17 is G or N, and X 18 is Y or D; a CDRL2 of formula (IV): (SEQ ID NO: 6) X 19 ASX 20 LAS wherein X 19 is S or E, and X 20 T or K; a CDRL3 has a formula (V): (SEO ID NO: 7) X 21 GX 22 X 23 SX 24 X 25 X 26 X 27 X 28 X 29 X 30 A wherein X 21 is L or Q, X 22 is G or E, X 23 is G or F, X 24 is C, S or G (particularly S or G), X 25 is S or G, X 26 is D, S or E, X 27 is H, G, A, S or C (particularly H, G, A or S), X 28 is I or D, X 29 is C, S or absent and X 30 is N or absent. 2 . (canceled) 3 . The antibody molecule according to claim 1 wherein formula (I) is SEQ ID NO: 8 or 11, such as SEQ ID NO: 8. 4 . The antibody molecule according to claim 1 , wherein formula (II) is SEQ ID NO: 9 or 12, such as SEQ ID NO: 9. 5 . The antibody molecule according to claim 1 , wherein CDRH3 is SEQ ID NO: 3 or 4. 6 . (canceled) 7 . The antibody molecule according to claim 1 , wherein formula (III) is SEQ ID NO: 13 or 19. 8 . The antibody molecule according to claim 1 , wherein formula (IV) is SEQ ID NO: 14 or 20. 9 . The antibody molecule according to claim 1 , wherein formula (V) is independently selected from the group comprising SEQ ID NO: 15, 16, 17, 18, 21, 22, 23 and 24. 10 . The antibody molecule according to claim 1 wherein CDR H1 is SEQ ID NO:8, CDR H2 is SEQ ID NO:9, CDRH3 is SEQ ID NO:4, CDRL1 is SEQ ID NO:13, CDRL2 is SEQ ID NO:14 and CDRL3 is independently selected from SEQ ID NO:15, 16, 17 or 18. 11 . The antibody molecule according to claim 1 wherein CDR H1 is SEQ ID NO:11, CDR H2 is SEQ ID NO:12, CDRH3 is SEQ ID NO:3, CDRL1 is SEQ ID NO:19, CDRL2 is SEQ ID NO:20 and CDRL3 is independently selected from SEQ ID NO:21, 22, 23 or 24. 12 . The antibody molecule according to any one of claim 1 , 3 - 5 , or 7 - 11 wherein VH and VL are humanised. 13 . The antibody molecule according to claim 12 wherein the variable domain of the heavy chain (VH) comprises a human framework region wherein the residue at at least one of positions 24, 37, 48, 49, 67, 71, 73 and 78 is a donor residue and the variable domain of the light chain (VL) comprises a human framework region wherein the residue at at least one of positions 2, 3, 36, 46, 49 and 70 is a donor residue. 14 . The antibody molecule according to claim 12 comprising a. a VH having the sequence given in SEQ ID NO:34 or 35 and a VL having the sequence given in SEQ ID NO:33 or 250 or b. a VH having the sequence given in SEQ ID NO:41 or 42 and a VL having the sequence given in SEQ ID NO:40, 341, 342 or 343. 15 . (canceled) 16 . The antibody molecule according to claim 12 , wherein the variable domain of the light chain comprises a sequence having at least 80% identity or similarity to the light chain variable domain of SEQ ID NO:33, 40 or 250 and wherein the variable domain of the heavy chain comprises a sequence having at least 80% identity or similarity to the heavy chain variable domain of SEQ ID NO:34, 35, 41 or 42. 17 . The antibody molecule according to any one of claims 1 to 16 wherein the antibody is: a. a full length antibody or b. a scFv, Fv, Fab or Fab′ fragment or c. a multispecific molecule such as a bispecific or trispecific. 18 - 19 . (canceled) 20 . The antibody molecule according to claim 1 , wherein the molecule format is selected from diabody, scdiabody, triabody, tandem scFv, FabFv, Fab′Fv, FabdsFv, Fab-scFv, Fab-dsscFv, Fab-(dsscFv) 2 diFab, diFab′, tribody, tandem scFv-Fc, scFv-Fc-scFv, scdiabody-Fc, scdiabody-CH3, Ig-scFv, scFv-Ig, V-Ig, Ig-V, Duobody and DVD-Ig. 21 . The antibody molecule according to claim 17 comprising one binding domain which is specific to CD79 and one binding domain which is specific to CD22 or CD45. 22 . The antibody molecule according to claim 21 wherein each binding domain is monospecific. 23 . The antibody molecule according to claim 21 wherein: a. the bispecific or trispecific molecule comprises no more than one binding domain which is specific to CD22 and no more than one binding domain which is specific to CD79a and/or CD79b; or b. the bispecific or trispecific molecule comprises no more than one binding domain which is specific to CD45 and no more than one binding domain which is specific to CD79a and/or CD79b, or c. the binding domain which is specific to CD22 or CD45 and the binding domain which is specific to CD79a and/or CD79b are independently selected from a Fab, scFv, Fv, dsFv and dsscFv.
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the tumour determinant being from a cell of a blood cancer · CPC title
against molecules with a "CD"-designation, not provided for elsewhere · CPC title
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