CTRI/2012/11/003145招募中2 期
A Multicenter, Randomized Study of the Efficacy and Safety of NVC-422 Ophthalmic Solution for the Treatment of Adenoviral Conjunctivitis
ovaBay Pharmaceutical Inc0 个研究点目标入组 440 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 440
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Subjects must be >= 18 years of age and <= 65 years of age
- •2. At least 1 eye (and in that same eye) must have onset and development of ocular symptoms and/or signs of conjunctivitis <= 3 days prior to enrollment (Day 1)
- •3. Females who are not pregnant and are not lactating.
- •4. Other inclusion criteria per protocol.
排除标准
- •1.Presence of subepithelial infiltrates (SEIs) at the Day 1 visit in either eye.
- •2.Suspected bacterial, fungal, herpes, Chlamydia or Acanthamoeba co-infection, based on clinical observation.
- •3.Subjects with ocular condition(s) that may interfere with the conduct of the study as outlined in the protocol.
- •4.Other exclusion criteria per protocol.
研究者
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