IP Library Patent Application 19062474
Patent Application
App. No. 19/062,474

ANTIBODIES CAPABLE OF BINDING TO OX40, VARIANTS THEREOF AND USES THEREOF

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Patent No.
US None
App. No.
19/062,474
Abstract

The present invention relates to antibodies capable of binding to human OX40 and to variants thereof comprising a modified Fc region comprising at least one mutation that enhances the Fc-Fc interaction of the antibody and at least one mutation that reduces the Fc effector functions of the antibody. The invention further provides pharmaceutical compositions comprising the antibodies and use of the antibodies for therapeutic and diagnostic procedures, in particular in cancer therapy.

Claims (25)

1 - 54 . (canceled)

55 . A nucleic acid or a set of nucleic acids encoding an antibody capable of binding to human OX40, wherein the antibody comprises,

a. an antigen-binding region comprising a heavy chain variable (VH) region wherein the CDR1, CDR2, and CDR3 comprising the sequences as set forth in SEQ ID NOs: 12, 13, and 14, respectively, and a light chain variable (VL) region wherein the CDR1, CDR2, and CDR3 comprising the sequences as set forth in SEQ ID NO: 16, DAS and 17, respectively, and

b. a human IgG1 Fc region comprising a P329R mutation and an E345R mutation, wherein the amino acid positions are numbered according to Eu numbering.

56 . An expression vector comprising the nucleic acids or set of nucleic acids of claim 55 .

57 . A recombinant host cell comprising the expression vector of claim 56 .

58 . The recombinant host cell of claim 57 , which is a eukaryotic cell.

59 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the Fc region is of the human IgG1mf, human IgG1ma, human IgG1mx or human IgG1mz allotype.

60 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the Fc region comprises the sequence set forth in SEQ ID NO: 3.

61 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the antibody is bivalent.

62 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the antibody is a monospecific, bispecific or multi-specific antibody.

63 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the antibody is a full-length antibody.

64 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the antibody has a heavy chain constant region comprising a sequence selected from the group comprising SEQ ID NOs: 58, 59, 60, and 61.

65 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the antibody has a heavy chain constant region comprising the sequence set forth in SEQ ID NO: 58.

66 . The nucleic acid or a set of nucleic acids of claim 55 , wherein the antibody comprises a heavy chain (HC) as set forth in SEQ ID NO: 18 and a light chain (LC) as set forth in SEQ ID NO: 19.

67 . A method of producing an antibody capable of binding to human OX40, the method comprising cultivating a recombinant host cell, the host cell comprising a nucleic acid or set of nucleic acids encoding the antibody, in a culture medium and under condition suitable for producing the antibody, and purifying or isolating the antibody from the culture medium, wherein the antibody comprises,

a. an antigen-binding region comprising a heavy chain variable (VH) region wherein the CDR1, CDR2, and CDR3 comprising the sequences as set forth in SEQ ID NOs: 12, 13, and 14, respectively, and a light chain variable (VL) region wherein the CDR1, CDR2, and CDR3 comprising the sequences as set forth in SEQ ID NO: 16, DAS and 17, respectively, and

b. a human IgG1 Fc region comprising a P329R mutation and an E345R mutation, wherein the amino acid positions are numbered according to Eu numbering.

68 . The method of claim 67 , wherein the Fc region is of the human IgG1mf, human IgG1ma, human IgG1mx or human IgG1mz allotype.

69 . The method of claim 67 , wherein the Fc region comprises the sequence set forth in SEQ ID NO: 3.

70 . The method of claim 67 , wherein the antibody is a full-length antibody.

71 . The method of claim 67 , wherein the antibody has a heavy chain constant region comprising a sequence selected from the group comprising SEQ ID NOs: 58, 59, 60, and 61.

72 . The method of claim 67 , wherein the antibody has a heavy chain constant region comprising the sequence set forth in SEQ ID NO: 58.

73 . The method of claim 67 , wherein the antibody comprises a heavy chain (HC) as set forth in SEQ ID NO: 18 and a light chain (LC) as set forth in SEQ ID NO: 19.

74 . A method of producing an antibody capable of binding to human OX40, the method comprising cultivating a recombinant host cell, the host cell comprising a nucleic acid or set of nucleic acids encoding the antibody, in a culture medium and under condition suitable for producing the antibody, and purifying or isolating the antibody from the culture medium, wherein the antibody comprises a heavy chain (HC) as set forth in SEQ ID NO: 18 and a light chain (LC) as set forth in SEQ ID NO: 19.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2025
From: BREIJ, ESTHER C. W.; GORLANI, ANDREA; GUELEN, LARS; KEMPER, KRISTEL; SATIJN, DAVID; VERZIJL, DENNIS; DE GOEJE, PAULINE LINDA; VAN DER KROEF, MAARTEN
To: GENMAB A/S
Reel/Frame 071626/0966 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2025
From: FELLERMEIER-KOPF, SINA; KÖHNE, MAREN; SAHIN, UGUR
To: BIONTECH SE
Reel/Frame 071627/0033 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2025
From: FELLERMEIER-KOPF, SINA; KÖHNE, MAREN; SAHIN, UGUR
To: BIONTECH SE
Reel/Frame 071627/0071 →