TEVA PHARMACEUTICAL INDUSTRIES LTD.;YEDA RESEARCH AND DEVELOPMENT CO. LTD.
发明人:
申请号：
IL16957405
公开号：
IL169574A
申请日:
2005.07.06
申请国别(地区):
IL
年份:
2015
代理人:
摘要：
The subject invention provides a pharmaceutical composition comprising: an aqueous carrier； from 0.1 mg/ml to 20 mg/ml of the composition of a pharmaceutically acceptable salt of a) a peptide comprising at least 12 and at most 30 consecutive amino acids having a sequence corresponding to (i) a sequence of amino acids found within a complementarity-determining region (CDR) of a heavy or a light chain of a human monoclonal anti-DNA 16/6 Id antibody, or (ii) a sequence of amino acids found within a complementarity-determining region (CDR) of a heavy or a light chain of a pathogenic anti-DNA monoclonal antibody that induces a systemic lupus erythematosus (SLE)-like disease response in mice, or b) a peptide comprising consecutive amino acids having the sequence shown by any of SEQ ID NOS. 8-17, or c) a peptide comprising consecutive amino acids having a sequence of any of a) and b), or at least two of the sequences in (a)(i), (a)(ii) and (b)(i) through (b)(x), or d) a peptide comprising consecutive amino acids having a sequence comprising at least two identical sequences included in (a)(i), (a)(ii) and (b)(i) through (b)(x)； and a solubility enhancer, wherein both the peptide and the solubility enhancer are dissolved in the aqueous carrier； and wherein the composition has a pH between 4 and 9, and a method of alleviating symptoms of SLE in a human by administering an effective amount of the composition.
