EUCTR2013-000133-12-IT进行中（未招募）1 期
A randomized controlled multicentre open-label parallel arm study to assess the non-inferiority of the safety of bevacizumab compared to ranibizumab (allocation 4:1) administered by intravitreal injection in patients with macular degeneration or other exudative not age-related macular - SBR-ITA13
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 1,780
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
- •1. Age-related macular degeneration
- •or Diabetic retinal oedema
- •or Retinal perivascular sheathing
- •or Choroidal neovascularisation
- •2. Men/woman
- •3. age = 18 years
- •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 280
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 1500
排除标准
- •1. Patients treated with anti-VEGF intravitreal within the last six months
- •prior the inclusion in the study
- •2. Pregnancy or breast-feending
- •3. Patients in emergency situation
- •4. Subjects inable to give informed consent
研究者
相似试验
进行中（未招募）
不适用
A controlled randomized open-label multicentre study evaluating if early initiation of everolimus (Certican®) and early elimination of cyclosporine (Sandimmun Neoral®) in de novo heart transplant recipients can improve long-term renal function and slow down the progression of chronic allograft vasculopathy. - SCHEDULEHeart transplantationMedDRA version: 14.1Level: PTClassification code 10019314Term: Heart transplantSystem Organ Class: 10042613 - Surgical and medical proceduresEUCTR2009-013074-41-DKovartis Healthcare A/S100
进行中（未招募）
1 期
A controlled randomized open-label multicentre study evaluating if early initiation of everolimus (Certican®)and early elimination of cyclosporine (Sandimmun Neoral®) in de novo heart transplant recipients can improve long-term renal function and slow down the progression of chronic allograft vasculopathy. - ScheduleHeart transplantationMedDRA version: 12.1Level: LLTClassification code 10019314Term: Heart transplantEUCTR2009-013074-41-NOovartis Norge AS
进行中（未招募）
不适用
A controlled randomized open-label multicentre study evaluating if early initiation of everolimus (Certican®)and early elimination of cyclosporine (Sandimmun Neoral®) in de novo heart transplant recipients can improve long-term renal function and slow down the progression of chronic allograft vasculopathy. - ScheduleEUCTR2009-013074-41-SEovartis Norge AS100
进行中（未招募）
不适用
A controlled randomized open-label multicentre study evaluatiing if early conversion to everolimus (Certican) from cyclosporine (Neoral) in de novo renal transplant receipients can improve long-term renal function and slow down the progression of chronic allograft nephropathy - CENTRAEUCTR2007-000771-42-SEovartis Pharma Services250
进行中（未招募）
不适用
A controlled randomized open-label multicentre study evaluatiing if early conversion to everolimus (Certican) from cyclosporine (Neoral) in de novo renal transplant receipients can improve long-term renal function and slow down the progression of chronic allograft nephropathy - CENTRAEUCTR2007-000771-42-DKovartis Pharma Services200