...
首页> 外文期刊>IDrugs: the investigational drugs journal >American Society of Hematology--48th Annual Meeting and Exposition. Updates on therapies. 9-12 December 2006 Orlando, FL, USA.
【24h】

American Society of Hematology--48th Annual Meeting and Exposition. Updates on therapies. 9-12 December 2006 Orlando, FL, USA.

机译:美国血液学会-第48届年会和博览会。治疗方法的更新。 2006年12月9日至12日,美国佛罗里达州奥兰多。

获取原文
获取原文并翻译 | 示例
           

摘要

In late 2005, MethylGene Inc reported the initiation of a phase I/II clinical trial to assess the histone deacetylase (HDAC) inhibitor MGCD-0103 (MethylGene Inc/Pharmion Corp/Taiho Pharmaceutical Co Ltd) in combination with the DNA methyltransferase inhibitor azacitidine in patients with advanced myelodysplastic syndrome (MDS) and acute myelogenous leukemia (AML). Guillermo Garcia-Manero (MD Anderson Cancer Center, USA) and colleagues presented results from the phase I portion of the clinical trial. This ongoing trial recruited 23 patients, 18 with AML and 5 with MDS, to receive 35, 60, 90, 110 or 135 mg of MGCD-0103 orally three times weekly (n = 3, 3, 8, 6 and 3, respectively; first dose on day 5 of the first cycle) plus 75 mg/m2/day of azacitidine subcutaneously for the first 7 days of each 28-day treatment cycle. At the time of this meeting, six of these patients were still being dosed, and one patient with AML had completed seven cycles.
机译:在2005年下半年,MethylGene Inc.报告开始了一项I / II期临床试验,以评估组蛋白脱乙酰基酶(HDAC)抑制剂MGCD-0103(MethylGene Inc / Pharmion Corp / Taiho Pharmaceutical Co Ltd)与DNA甲基转移酶抑制剂azacitidine的组合。患有晚期骨髓增生异常综合症(MDS)和急性骨髓性白血病(AML)的患者。 Guillermo Garcia-Manero(美国MD安德森癌症中心)及其同事介绍了该临床试验第一阶段的结果。这项正在进行的试验招募了23名患者,其中AML为18例,MDS为5例,每周三次口服35、60、90、110或135 mg MGCD-0103(n = 3、3、8、6和3;在每个28天治疗周期的前7天中,皮下注射75mg / m2 /天的阿扎胞苷,并在第一个周期的第5天服用第一剂。在会议召开之时,这些患者中有6名仍在服药,一名AML患者已完成7个周期。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号