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    • 3. 发明授权
    • Pharmaceutical antibody compositions with resistance to soluble CEA
    • 具有抗CEA抗性的药物抗体组合物
    • US08901278B2
    • 2014-12-02
    • US13324823
    • 2011-12-13
    • Doris RauSusanne MangoldPeter KuferTobias Raum
    • Doris RauSusanne MangoldPeter KuferTobias Raum
    • C07K16/30A61K39/00
    • C07K16/3007A61K2039/505C07K2317/24C07K2317/56C07K2317/565C07K2317/622C07K2317/732
    • The present invention relates to pharmaceutical compositions for the treatment of an epithelial tumor in a human, said pharmaceutical composition comprising an IgG1 antibody specifically binding to human CEA, wherein the variable region of said IgG1 antibody comprises at least (i) a CDR-H1 having the amino acid sequence “SYWMH” (SEQ ID NO: 29) and a CDR-H2 having the amino acid sequence “FIRNKANGGTTEYAASVKG” (SEQ ID NO: 28) and a CDR-H3 having the amino acid sequence “DRGLRFYFDY” (SEQ ID NO: 27) or (ii) a CDR-H1 having the amino acid sequence “TYAMH” (SEQ ID NO: 31) and a CDR-H2 having the amino acid sequence “LISNDGSNKYYADSVKG” (SEQ ID NO: 30) and a CDR-H3 having the amino acid sequence “DRGLRFYFDY” (SEQ ID NO: 27). Furthermore, processes for the production of said pharmaceutical compositions as well as medical/pharmaceutical uses for the IgG1 antibody molecules bearing specificities for the human CEA antigen are disclosed.
    • 本发明涉及用于治疗人类上皮肿瘤的药物组合物,所述药物组合物包含与人CEA特异性结合的IgG1抗体,其中所述IgG1抗体的可变区至少包含(i)具有 氨基酸序列“SYWMH”(SEQ ID NO:29)和具有氨基酸序列“FIRNKANGGTTEYAASVKG”(SEQ ID NO:28)的CDR-H2和具有氨基酸序列“DRGLRFYFDY”(SEQ ID NO: (SEQ ID NO:31)的CDR-H1和具有氨基酸序列“LISNDGSNKYYADSVKG”(SEQ ID NO:30)的CDR-H2和CDR -H3,具有氨基酸序列“DRGLRFYFDY”(SEQ ID NO:27)。 此外,公开了用于生产所述药物组合物的方法以及具有人CEA抗原特异性的IgG1抗体分子的医疗/药物用途。