摘要:
This present invention describes the derivation and selection of antibodies capable of neutralising the major exotoxins; TcdA and TcdB of Clostridium difficile. The invention also describes novel neutralisation and antigen binding properties of individual Mabs and mixtures thereof.
摘要:
This present invention describes the derivation and selection of antibodies capable of neutralising the major exotoxins; TcdA and TcdB of Clostridium difficile. The invention also describes novel neutralisation and antigen binding properties of individual Mabs and mixtures thereof.
摘要:
The invention relates to antibody molecules having specificity for antigenic determinants of human IL-13, therapeutic uses of the antibody molecules and methods for producing said antibody molecules.
摘要:
The invention relates to antibody molecules having specificity for antigenic determinants of human IL-13, therapeutic uses of the antibody molecules and methods for producing said antibody molecules.
摘要:
A humanised agonistic antibody which binds human PD-1 comprising a heavy chain and a light chain wherein the variable domain of the heavy chain comprises the sequence given in SEQ ID NO:1 for CDR-H1, the sequence given in SEQ ID NO:2 for CDR-H2 and the sequence given in SEQ ID NO:3 for CDR-H3 and the variable domain of the light chain comprises the sequence given in SEQ ID NO:4 for CDR-L1, the sequence given in SEQ ID NO:5 for CDR-L2 and the sequence given in SEQ ID NO:7 for CDR-L3. The invention also extends to therapeutic uses of the antibody molecules, compositions and methods for producing said antibody molecules.
摘要翻译:结合包含重链和轻链的人PD-1的人源化激动抗体,其中重链的可变结构域包含SEQ ID NO:1中针对CDR-H1给出的序列,SEQ ID NO:2中给出的序列 对于CDR-H2和CDR-H3的SEQ ID NO:3中给出的序列,轻链的可变结构域包含SEQ ID NO:4中针对CDR-L1给出的序列,SEQ ID NO:5中给出的序列 对于CDR-L2和针对CDR-L3的SEQ ID NO:7中给出的序列。 本发明还延伸到抗体分子的治疗用途,用于产生所述抗体分子的组合物和方法。
摘要:
The present invention relates to improved methods for the selection of appropriate human acceptor framework regions for non-human (donor) antibodies and methods for obtaining humanized antibodies of high affinity using such acceptor frameworks.
摘要:
The present invention relates to improved methods for the selection of appropriate human acceptor framework regions for non-human (donor) antibodies and methods for obtaining humanized antibodies of high affinity using such acceptor frameworks.
摘要:
A humanised agonistic antibody which binds human PD-1 comprising a heavy chain and a light chain wherein the variable domain of the heavy chain comprises the sequence given in SEQ ID NO:1 for CDR-H1, the sequence given in SEQ ID NO:2 for CDR-H2 and the sequence given in SEQ ID NO:3 for CDR-H3 and the variable domain of the light chain comprises the sequence given in SEQ ID NO:4 for CDR-L1, the sequence given in SEQ ID NO:5 for CDR-L2 and the sequence given in SEQ ID NO:7 for CDR-L3. The invention also extends to therapeutic uses of the antibody molecules, compositions and methods for producing said antibody molecules.
摘要翻译:结合包含重链和轻链的人PD-1的人源化激动抗体,其中重链的可变结构域包含SEQ ID NO:1中针对CDR-H1给出的序列,SEQ ID NO:2中给出的序列 对于CDR-H2和CDR-H3的SEQ ID NO:3中给出的序列,轻链的可变结构域包含SEQ ID NO:4中针对CDR-L1给出的序列,SEQ ID NO:5中给出的序列 对于CDR-L2和针对CDR-L3的SEQ ID NO:7中给出的序列。 本发明还延伸到抗体分子的治疗用途,用于产生所述抗体分子的组合物和方法。