THERAPEUTIC CHEMOKINE RECEPTOR ANTAGONISTS
    5.
    发明授权
    THERAPEUTIC CHEMOKINE RECEPTOR ANTAGONISTS 有权
    治疗性趋化因子受体拮抗剂

    公开(公告)号:EP1061944B1

    公开(公告)日:2004-01-28

    申请号:EP99908703.4

    申请日:1999-03-12

    摘要: The invention provides a variety of therapeutic uses for CXCR4 antagonists. In various embodiments, CXCR4 antagonists may be used as therapeutically as follows, or to manufacture a medicament for such therapeutic treatments: reducing interferon gamma production by T-cells, treatment of an autoimmune disease, treatment multiple sclerosis, treatment of cancer, inhibition of angiogenesis. The invention provides corresponding methods of medical treatment, in which a therapeutic dose of a CXCR4 antagonist is administered in a pharmacologically acceptable formulation. Accordingly, the invention also provides therapeutic compositions comprising a CXCR4 antagonist and a pharmacologically acceptable excipient or carrier. The CXCR4 antagonists for use in the invention may be peptide compounds comprising a substantially purified peptide fragment, modified fragment, analogue or pharmacologically acceptable salt of SDF-1.

    THERAPEUTIC CHEMOKINE RECEPTOR ANTAGONISTS
    6.
    发明公开
    THERAPEUTIC CHEMOKINE RECEPTOR ANTAGONISTS 有权
    治疗性趋化因子受体拮抗剂

    公开(公告)号:EP1061944A2

    公开(公告)日:2000-12-27

    申请号:EP99908703.4

    申请日:1999-03-12

    IPC分类号: A61K38/21 C07K14/52

    摘要: The invention provides a variety of therapeutic uses for CXCR4 antagonists. In various embodiments, CXCR4 antagonists may be used as therapeutically as follows, or to manufacture a medicament for such therapeutic treatments: reducing interferon gamma production by T-cells, treatment of an autoimmune disease, treatment multiple sclerosis, treatment of cancer, inhibition of angiogenesis. The invention provides corresponding methods of medical treatment, in which a therapeutic dose of a CXCR4 antagonist is administered in a pharmacologically acceptable formulation. Accordingly, the invention also provides therapeutic compositions comprising a CXCR4 antagonist and a pharmacologically acceptable excipient or carrier. The CXCR4 antagonists for use in the invention may be peptide compounds comprising a substantially purified peptide fragment, modified fragment, analogue or pharmacologically acceptable salt of SDF-1.