跳至主要内容
临床试验/NCT00327535
NCT00327535已完成2 期

A Multicenter, Randomized, Open Label Dose Finding Study of Mircera in Anemic Patients With Stage IIIB or IV Non-small Cell Lung Cancer Receiving First Line Myelosuppressive Chemotherapy

Hoffmann-La Roche0 个研究点目标入组 153 人开始时间: 2006年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
153
主要终点
Average Hb change from baseline

研究概览

简要总结

This 4 arm study will assess the optimal starting dose of Mircera in the treatment of anemia in patients with non-small cell lung cancer receiving first line myelosuppressive chemotherapy. Patients will be randomized to receive either Mircera 6.3 micrograms/kg, 9 micrograms/kg or 12 micrograms/kg s.c. every 3 weeks or darbepoetin alfa according to the approved local label (either 6.75 micrograms/kg s.c. every 3 weeks, or 2.25 micrograms/kg every week). The anticipated time on study treatment is <3 months and the target sample size is 100-500 individuals.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • >=18 years of age;
  • stage III or IV non-small cell lung cancer receiving first line myelosuppressive chemotherapy;
  • myelosuppressive chemotherapy scheduled for at least 9 weeks;
  • anemia at screening visit.

排除标准

  • transfusion of red blood cells during the 4 weeks prior to first planned dose of study medication;
  • iron deficiency anemia, or anemia caused by gastrointestinal bleeding;
  • prior treatment with Mircera.

研究组 & 干预措施

Mircera 6.3 micrograms/kg

Experimental

干预措施: methoxy polyethylene glycol-epoetin beta [Mircera] (Drug)

Mircera 9 micrograms/kg

Experimental

干预措施: methoxy polyethylene glycol-epoetin beta [Mircera] (Drug)

Mircera 12 micrograms/kg

Experimental

干预措施: methoxy polyethylene glycol-epoetin beta [Mircera] (Drug)

Darbepoetin alfa

Active Comparator

干预措施: Darbepoetin alfa (Drug)

结局指标

主要结局

Average Hb change from baseline

时间窗: Weeks 5-13

次要结局

  • Target Hb therapeutic range, average Hb values, hematopoietic response.(Days 2-85)
  • Red blood cell (RBC) transfusions(Weeks 5-13)
  • Adverse events (AEs), laboratory parameters, premature withdrawals(Throughout study)

研究者

申办方类型
Industry
责任方
Sponsor

相似试验