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    • 3. 发明申请
    • USE OF SAPACITABINE TO TREAT PROLIFERATIVE DISEASE
    • 使用SAPACITABINE治疗增殖性疾病
    • WO2008132443A1
    • 2008-11-06
    • PCT/GB2008/001424
    • 2008-04-24
    • CYCLACEL LIMITEDCHIAO, Judy
    • CHIAO, Judy
    • A61K31/513A61P35/00
    • A61K31/7068A61K31/513
    • One aspect of the present invention relates to the use of sapacitabine, or a metabolite thereof, in the preparation of a medicament for treating a proliferative disorder, wherein the sapacitabine or metabolite thereof is administered in a dosing regimen comprising at least one treatment cycle, wherein said treatment cycle comprises administering a therapeutically effective amount of sapacitabine or metabolite thereof for about 2 to about 6 days per week, for 2 weeks out of 3 weeks. Another aspect of the invention relates to the use of sapacitabine, or a metabolite thereof, in the preparation of a medicament for treating cutaneous T-cell lymphoma (CTCL).
    • 本发明的一个方面涉及用于制备用于治疗增殖性病症的药物中的西他滨或其代谢物的用途,其中所述的沙美他滨或其代谢物以包含至少一个治疗周期的给药方案施用,其中 所述治疗周期包括在3周内给予治疗有效量的每周约2至约6天的治疗有效量的沙美他滨或其代谢物2周。 本发明的另一方面涉及用于制备用于治疗皮肤T细胞淋巴瘤(CTCL)的药物的西他滨或其代谢物的用途。
    • 4. 发明申请
    • DOSAGE REGIMEN FOR SAPACITABINE AND DECITABINE IN COMBINATION FOR TREATING ACUTE MYELOID LEUKEMIA
    • 用于治疗急性髓性白血病的组合中的SAPACITABINE和组合的剂量
    • WO2012140436A1
    • 2012-10-18
    • PCT/GB2012/050815
    • 2012-04-13
    • CYCLACEL LIMITEDCHIAO, Judy
    • CHIAO, Judy
    • A61K31/706A61K31/7068A61P35/02
    • A61K31/7068A61K31/706A61K2300/00
    • A first aspect of the invention relates to a method of treating AML in a subject, said method comprising administering to a subject a therapeutically effective amount of (i) sapacitabine, or a metabolite thereof; and (ii) decitabine; in accordance with a dosing regimen comprising at least one first treatment cycle and at least one second treatment cycle, wherein said first treatment cycle comprises administering a therapeutically effective amount of decitabine for 5 to 10 consecutive days followed by a rest period of from 3 to 5 weeks, or until treatment-related toxicities are resolved, whichever is longer; and wherein said second treatment cycle comprises administering a therapeutically effective amount of sapacitabine, or a metabolite thereof, for 3 consecutive days per week, for 2 weeks followed by a rest period of from 2 to 4 weeks, or until treatment- related toxicities are resolved, whichever is longer.
    • 本发明的第一方面涉及一种在受试者中治疗AML的方法,所述方法包括向受试者施用治疗有效量的(i)西他滨或其代谢物; 和(ii)地西他滨; 根据包含至少一个第一治疗​​周期和至少一个第二治疗周期的给药方案,其中所述第一治疗周期包括施用治疗有效量的地西他滨连续5至10天,随后休息期为3至5 周,或直到治疗相关毒性得到解决,以较长者为准; 并且其中所述第二治疗周期包括每周连续3天施用治疗有效量的沙美他滨或其代谢物2周,然后2至4周的休息期,或直到治疗相关毒性被解决 ,以较长者为准。