THERAPEUTIC USES OF ALLOGENEIC MYELOID PROGENITOR CELLS
    3.
    发明申请
    THERAPEUTIC USES OF ALLOGENEIC MYELOID PROGENITOR CELLS 有权
    治疗性甲状腺激素原细胞的治疗方法

    公开(公告)号:US20150174167A1

    公开(公告)日:2015-06-25

    申请号:US14642254

    申请日:2015-03-09

    Abstract: Myeloid function is enhanced by transplantation or infusion of allogeneic myeloid progenitor cells, including CMP, GMP, MEP and MKP cell subsets. Myeloid progenitors ameliorate sequelae of anemia and thrombocytopenia, and can prevent or treat gastrointestinal mucositis associated with chemotherapy, radiotherapy, and the like. The transplantation or infusion may be performed in the absence of HLA typing, and the cells may be mismatched at one or more Class I HLA loci. The transplantation may provide for treatment of ongoing disease, or prevention of disease in high risk patients.

    Abstract translation: 通过移植或输注同种异体骨髓祖细胞(包括CMP,GMP,MEP和MKP细胞亚群)增强骨髓功能。 骨髓祖细胞改善贫血和血小板减少症的后遗症,并可预防或治疗与化疗,放疗等相关的胃肠道粘膜炎。 可以在不存在HLA分型的情况下进行移植或输注,并且细胞可能在一个或多个I类HLA基因座处不匹配。 该移植可以提供治疗正在进行的疾病或预防高危患者的疾病。

    Method of reducing deleterious effects of ischemia by administration of a thrombopoietin receptor ligand
    6.
    发明授权
    Method of reducing deleterious effects of ischemia by administration of a thrombopoietin receptor ligand 有权
    通过给予血小板生成素受体配体减少缺血的有害作用的方法

    公开(公告)号:US08518883B2

    公开(公告)日:2013-08-27

    申请号:US12971678

    申请日:2010-12-17

    CPC classification number: A61K38/196

    Abstract: A therapeutic or prophylactic treatment method of ischemia, such as due to myocardial infarction, by administering thrombopoietin, alone or in combination with other drugs, to a patient suffering from or at risk of cardiac injury, such as myocardial ischemia. The thrombopoietin is administered in a concentration such that the subject's platelet count or production of platelets is not significantly affected.

    Abstract translation: 通过将血小板生成素单独或与其它药物组合施用于患有或有心脏损伤风险的患者(例如心肌缺血)的局部缺血的治疗或预防治疗方法,例如由于心肌梗塞。 血小板生成素的给药浓度使得受试者的血小板计数或血小板的产生不受显着影响。

Patent Agency Ranking