EUCTR2011-003191-36-IT进行中(未招募)1 期
Dose-dense ABVD as first line therapy in early stage unfavorable Hodgkin’s Lymphoma: a phase II, prospective, multi-center study - FIL-DDABVD
FONDAZIONE ITALIANA LINFOMI ONLUS0 个研究点目标入组 86 人开始时间: 2012年3月7日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 86
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
- All
入选标准
- •Age 18-70 years • Histologically confirmed HL stage I, II unfavorable according to EORTC criteria, with exclusion of stage II B bulky. • Previously untreated • ECOG performance status 0 - 2 • Staging with FDG-PET • Written informed consent • Adequate liver and renal function (total serum bilirubin < 2.5 x ULN, AST/SGOT and/or ALT/SGPT = 2.5 x upper limit of normal (ULN) or = 5.0 x ULN if the transaminase elevation is due to disease involvement, serum creatinine < 2.5 x ULN)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 81
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 5
排除标准
- •Concomitant cardiac, pulmonary, neurologic, psychiatric or metabolic severe disease. • Uncontrolled diabetes mellitus (with fasting glucose levels above 200 mg/dl). • Other prior malignancies except for adequately treated basal cell carcinoma, squamous cell carcinoma of the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast or other cancer from which the patient has been disease-free for = 3 years • Patients with a known history of HIV seropositivity • Active HCV infection ( PCR + ; AST> 1.5-2x UN) • Woman who is pregnant or breast feeding. Fertile patients not willing to use effective contraception during the study and 3 months after the end of treatment. Women of childbearing potential (WOCBP) are defined as sexually mature women who have not undergone a hysterectomy or who have not been naturally postmenopausal for at least 12 consecutive months. Negative pregnancy test at baseline is required (serum???HCG). • Male patient whose sexual partner(s) are WOCBP who are not willing to use a effective contraception during the study and 3 months after the end of treatment • Nodular lymphocyte prevalence histological subtype
研究者
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