跳至主要内容
临床试验/ISRCTN52817670
ISRCTN52817670已完成3 期

A randomised two-arm, prospective, multi-centre, open-label phase III trial comparing the activity and safety of a weekly versus a three-weekly paclitaxel treatment schedule in patients with advanced or metastatic breast cancer

Anglo Celtic Cooperative Oncology Group (UK)0 个研究点目标入组 600 人开始时间: 2002年10月15日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
600

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

性别
Female

入选标准

  • 1. Histologically proven breast cancer
  • 2. Locally advanced or metastatic disease
  • 3. Presence of measurable or evaluable lesions
  • 4. Prior treatment with anthracyclines (either in the adjuvant setting or for metastatic disease) or contraindication to anthracyclines
  • 5. Aged 18 years or greater
  • 6. World Health Organization (WHO)/Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 2
  • 7. Adequate haematological, renal and hepatic function
  • 8. Written informed consent

排除标准

  • Not provided at time of registration

研究者

发起方
Anglo Celtic Cooperative Oncology Group (UK)

相似试验

进行中(未招募)
不适用
A prospective, multi-centre, randomised, double-blind, placebo-controlled comparison of intravenous dexmedetomidine with haloperidol in treatment of hyperactive delirium after heart surgery. - Dex-in-delirPostoperative hyperactive deliriumMedDRA version: 12.0Level: LLTClassification code 10000702Term: Acute deliriumMedDRA version: 12.0Level: LLTClassification code 10049989Term: Agitation postoperativeMedDRA version: 12.0Level: LLTClassification code 10056436Term: Psychomotor agitationMedDRA version: 12.0Level: LLTClassification code 10049987Term: Confusion postoperative
EUCTR2008-007384-17-SESten Walther75
进行中(未招募)
1 期
Randomized, multicentre, prospective, two-arm, open-label Phase II study to investigate the efficacy and safety of two ZK219477 i.v. infusions (3-hour infusion of 16mg/m2 versus 0.5-hour infusion of 16mg/m2) in patients with recurrent ovarian cancer progressing during, or within 6 months of the end of platinum-based chemotherapy
EUCTR2005-000635-15-GBSchering AG
进行中(未招募)
3 期
A comparative clinical trial to understand efficacy and safety of R-TPR-012/ Metalyse® in Patients with heart attack
CTRI/2016/09/007230Reliance Life sciences Pvt Ltd
已完成
3 期
Efficacy of strontium ranelate versus placebo on the time to fracture healing in osteoporotic men and osteoporotic post-menopausal womeRadius fracture, OsteoporosisMusculoskeletal DiseasesOsteoporosis with pathological fracture
ISRCTN51868986Institut de Recherches Internationales Servier (France)217
进行中(未招募)
不适用
A multi-centre, open-label, randomised, two-arm Phase III trial of bevacizumab plus chemotherapy versus chemotherapy alone in patients with platinum-resistant, epithelial ovarian, fallopian tube or primary peritoneal cancer. - AureliaPlatinum-resistant, epithelial ovarian, fallopian tube or primary peritoneal cancer.MedDRA version: 9.1Level: LLTClassification code 10033128MedDRA version: 9.1Level: LLTClassification code 10016180MedDRA version: 9.1Level: LLTClassification code 10061344
EUCTR2009-011400-33-ITF. Hoffmann - La Roche Ltd300