跳至主要内容
临床试验/CTRI/2008/091/000016
CTRI/2008/091/000016招募中3 期

Phase III Randomized Trial of Maintenance Pegylated Liposomal Doxorubicin (PLD) / Carboplatin versus without in Patients with Advanced Ovarian Cancer

TTY Biopharm Company Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • •a.histologically proven ovarian cancer of FIGO stage III/IV
  • •b.treatment with five to six cycles of Paclitaxel / Platinum regimen
  • •c.attainment of a clinical defined complete response (ie, no cancer-related symptom ; normal physical examination, CT scan of the abdominal/pelvis and chest x-ray ; CA-125 level  35 U/mL)
  • •d.performance status of ECOG 0, 1, 2
  • •e.adequate hematopoietic function is defined as below:
  • •ANC  1,500/uL
  • •Platelets  100,000/uL
  • •f.adequate organ function is defined as below:
  • •Total bilirubin  1.5  ULN
  • •ALT / AST  1.5  ULN (5.0 x ULN if hepatic metastasis)
  • •Serum creatinine ≦ 1.5 × ULN
  • •g.age 20-75 years old
  • •h.life expectancy equal or longer than 3 months
  • •i.ability to understand and willingness to sign a written informed consent document

排除标准

  • •a.presence of CNS metastases (including clinical suspicion)
  • •b.other malignancy with exception of curative treated non-melanoma skin cancer or cervical carcinoma in situ within 5 years prior to entering the study
  • •c.presence of other serious concomitant illness which can affect or elevate the value of CA-125, e.g.;
  • •Autoimmune disease
  • •Sarcoidosis
  • •Chronic active hepatitis
  • •Pericarditis
  • •Cirrhosis of liver
  • •Abdominal tuberculosis
  • •Pancratitis
  • •d.presence of other serious concomitant illness which might be aggravated by study medication:
  • •Uncontrolled infection (active serious infections that are not controlled by antibiotics)
  • •Active cardiac disease e.g. decompensate myocardial infarction within the 6-month period preceding entry into the study.
  • •History of ventricular arrhythmia or congestive heart failure.
  • •e.surgery within 2 weeks prior to entering the study
  • •f.radiotherapy within 4 weeks prior to entering the study
  • •g.concurrent chemotherapy, radiotherapy, or other investigational drug except non-disease related conditions (e.g. insulin for diabetes) during study period
  • •h.mental status is not fit for clinical trial
  • •i.pregnant or breast feeding women
  • •j.potential child-bearing women unless using a reliable and appropriate contraceptive method.

研究者

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