发明名称 Methods of treating Kawasaki disease using IL-1beta antibodies
摘要 This invention relates to a novel use of IL-1β-ligand/IL-1 receptor disrupting compounds (herein referred to as “IL-1beta Compounds”); such as small molecular compounds disrupting IL-1b ligand-IL-1 receptor interaction, IL-1b antibodies or IL-1 receptor antibodies, e.g. IL-1b binding molecules described herein, e.g. antibodies disclosed herein, e.g. IL-1b binding compounds or IL-1 receptor binding compounds, and/or RNA compounds decreasing either IL-1b ligands or IL-1 receptor protein levels, in the treatment and/or prevention of auto-inflammatory syndromes, e.g. Juvenile rheumatoid arthritis or adult rheumatoid arthritis syndrome and to methods of treating and/or preventing auto-inflammatory syndromes, e.g. Juvenile rheumatoid arthritis or adult rheumatoid arthritis syndrome, in mammals, particularly humans.
申请公布号 US9534047(B2) 申请公布日期 2017.01.03
申请号 US201514861191 申请日期 2015.09.22
申请人 Novartis AG 发明人 Gram Hermann;Jung Thomas
分类号 C07K16/24;A61K39/395;A61K39/00 主分类号 C07K16/24
代理机构 Leslie Fischer 代理人 Leslie Fischer
主权项 1. A method of treating Kawasaki Disease in a patient in need thereof, comprising administering to said patient an effective amount of a human IL-1 beta binding antibody comprising an antigen binding site comprising: a) at least one immunoglobulin heavy chain variable domain (VH) which comprises in sequence hypervariable regions CDR1, CDR2 and CDR3, said CDR1 comprising the amino acid sequence set forth as SEQ ID NO:3, said CDR2 comprising the amino acid sequence set forth as SEQ ID NO:4, and said CDR3 comprising the amino acid sequence set forth as SEQ ID NO:5; and b) at least one immunoglobulin light chain variable domain (VL) which comprises in sequence hypervariable regions CDR1′, CDR2′ and CDR3′, said CDR1 comprising the amino acid sequence set forth as SEQ ID NO:6, said CDR2′ comprising the amino acid sequence set forth as SEQ ID NO:7, said CDR3′ comprising the amino acid sequence set forth as SEQ ID NO:8,wherein said antibody is parenterally administered at a dose between 0.1-50 mg of said antibody per kg body weight of the patient.
地址 Basel CH