USE OF HISTONE DEACETYLASE INHIBITORS FOR THE CARE OF PHILADELPHIA-NEGATIVE MYELOPROLIFERATIVE SYNDROMES
    1.
    发明申请
    USE OF HISTONE DEACETYLASE INHIBITORS FOR THE CARE OF PHILADELPHIA-NEGATIVE MYELOPROLIFERATIVE SYNDROMES 审中-公开
    乙酰脱乙酰基酶抑制剂用于治疗儿童肾上腺髓质增生综合征

    公开(公告)号:US20170049740A1

    公开(公告)日:2017-02-23

    申请号:US15346926

    申请日:2016-11-09

    Abstract: The use of substances capable of inhibiting one or more enzymes of the histone deacetylase family (histone deacetylase inhibitors) for the therapeutic treatment of Philadelphia-negative myeloproliferative syndromes (polycythemia vera, essential thrombocythemia or idiopathic myelofibrosis) is described. The dosage of the above-mentioned substances is significantly lower than that normally used for the care of other tumour syndromes and may be from 10 to 150 mg/day/patient.

    Abstract translation: 描述了能够抑制组蛋白脱乙酰酶家族的一种或多种酶(组蛋白脱乙酰酶抑制剂)用于费城阴性骨髓增生综合征(真性红细胞增多症,原发性血小板增多症或特发性骨髓纤维化)的治疗性治疗的物质的使用。 上述物质的剂量明显低于通常用于其他肿瘤综合征的治疗剂量,并且可以为10至150mg /天/患者。

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