A Multicenter, Randomized, Double-blind, Parallel-controlled Phase I Trial Comparing the Safety, Pharmacokinetics and Efficacy of 9MW0813 and Aflibercept (EYLEA®) After a Single Dose in Patients With Diabetic Macular Edema (DME)
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 24
- 试验地点
- 1
- 主要终点
- Incidence of adverse events
研究概览
简要总结
A multicenter, randomized, double-blind, parallel-controlled phase I trial comparing the safety, pharmacokinetics and efficacy of 9MW0813 and aflibercept (EYLEA®) after a single dose in patients with diabetic macular edema (DME).
详细描述
This is a multi-center, randomized, double-blind, parallel controlled Phase I clinical trial.
The primary objective is to compare the safety of a single intravitreal injection (IVT) of 9MW0813 injection and aflibercept intraocular injection solution (EYLEA®) in DME patients.
The secondary objectives are to comparing the pharmacokinetic profile, immunogenicity and efficacy of a single intravitreal injection (IVT) of 9MW0813 injection and aflibercept intraocular injection solution (EYLEA®) in DME patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
9MW0813
干预措施: 9MW0813 (Drug)
aflibercept
干预措施: Aflibercept (Drug)
结局指标
主要结局
Incidence of adverse events
时间窗: baseline to week 6
次要结局
- Area under the plasma concentration versus time curve (AUC) of 9MW0813 and aflibercept(baseline to week 6)
- Change from Baseline in Best Corrected Visual Acuity (BCVA)(baseline to week 6)
- Peak Plasma Concentration（Cmax） of 9MW0813 and aflibercept(baseline to week 6)
- Immunogenicity of IVT injection of 9MW0813 and aflibercept(baseline to week 6)