发明名称 Pharmaceutical compositions for binding sphingosine-1-phosphate
摘要 The present invention relates to compositions that comprise an anti-S1P monoclonal antibody, antibody fragment, or derivative in a carrier, particularly a buffered, hypertonic aqueous solution, as well as to kits containing such compositions, and methods for using such compositions for treatment of diseases and conditions associated with S1P.
申请公布号 US9181331(B2) 申请公布日期 2015.11.10
申请号 US200912418597 申请日期 2009.04.05
申请人 Lpath, Inc. 发明人 Sabbadini Roger A.;Pancoast Scott R.;Hansen Genevieve;Garland William A.;Safonov Marina
分类号 A61K39/395;C07K16/00;C07K16/18 主分类号 A61K39/395
代理机构 Acuity Law Group, P.C. 代理人 Acuity Law Group, P.C. ;Chambers Daniel M.
主权项 1. A composition comprising a pharmaceutically acceptable carrier and an antibody or an antigen-binding antibody fragment that binds sphingosine-1-phosphate (S1P) under physiological conditions, wherein the composition is hypertonic and the antibody or an antigen-binding antibody fragment comprises at least one heavy chain variable domain and at least one light chain variable domain, wherein: A. each heavy chain variable domain comprises: (i) a first sequence of amino acid residues of sequence DHTIH (SEQ ID NO: 4);(ii) a second sequence of amino acid residues selected from the group consisting of AISPRHDITKYNEMFRG (SEQ ID NO: 6); and(iii) a third sequence of amino acid residues of sequence GGFYGSTIWFDF (SEQ ID NO: 5); and B. each light chain variable domain comprises the following: (i) a first sequence of amino acid residues of sequence ITTTDIDDDMN (SEQ ID NO: 1);(ii) a second sequence of amino acid residues of sequence EGNILRP (SEQ ID NO: 2); and(iii) a third sequence of amino acid residues of sequence LQSDNLPFT (SEQ ID NO: 3),wherein the composition comprises a buffered hypertonic solution having a pH between about pH 5.5 and about pH 6.5 and comprising sodium chloride in a concentration of at least about 250mM.
地址 San Diego CA US
您可能感兴趣的专利