EUCTR2020-005875-10-BG进行中（未招募）1 期
An Extension Study to Evaluate the Long-Term Outcomes of Patients Who Received Treatment for Retinopathy of Prematurity in the VGFTe-ROP-1920 Study - BUTTERFLEYE NEXT
Regeneron Pharmaceuticals. Inc.0 个研究点目标入组 112 人开始时间: 2021年12月3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
- 112
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
- •Key Inclusion Criteria:
- •1. Patient was treated in study VGFTe-ROP-1920
- •2. Age <13 months of chronological age
- •3. Signed informed consent from parent(s)/legal guardian(s), which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 112
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Patient has a condition preventing participation in the study, or performance of study
研究者
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