EUCTR2004-001103-35-DK进行中(未招募)不适用
Exemestane in Advanced or Recurrent Endometrial Carcinoma.A multicentre non-randomized Phase II study
ordic Society for Gynecologic Oncology0 个研究点目标入组 70 人开始时间: 2007年1月26日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 70
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Advanced endometrial cancer (stage III-IV), not considered for treatment modalities apart from hormonal treatment
- •Relapse after primary treatment with interval > 1 month
- •Measurable tumour by X-ray examination and/or CT and/or MRI outside irradiated area.
- •Histological verified endometrial cancer. Only patients with tumors of endometrioid type will be accepted.
- •Post-menopausal women
- •Expected survival > 6 month
- •Age must be at least 18 years
- •Performance status must be 0-2 (WHO/ECOG, appendix I)
- •Informed consent given according to ICH/EU GCP guidelines and local or national laws
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Congestive heart failure grade III-IV
- •Severe hepatic or renal impairment not allowing for adequate use of the proposed regimens. ASAT or ALAT > 4 times of the upper limit of the normal values. S-Creatinine >150 mmol/l
- •Other malignancies within the last 5 years apart from cancer in situ cervicis uteri or basal cell carcinoma of the skin.
- •History of tromboembolic signs.
- •Any treatment that interact with the study drug like carbamazepine or cyclosporine.
- •Other primary hormonal therapy.
- •Tumors consisting of or with elements of serous papillary (UPSC) or clear cell type.
- •Inclusion in other trials.
- •Any cancer treatment or use of any investigation agent within one month of the study entry.
- •Circumstances at the time of the entry that would not permit completion of the study or follow-up.
- •Patients with symptomatic brain metastases.
- •Pregnancy, lactation or child bearing potential patients without adequate contraception
- •Dementia or significantly altered status that would prohibit the understanding and giving of informed consent.
研究者
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