Randomized, Double-Masked, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of IRX-101 Versus 5% Povidone-Iodine as an Ocular Surface Sterilizer
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 5
- 试验地点
- 1
- 主要终点
- Incidence of infectious endophthalmitis after topical use of IRX-101 combined with IVT
研究概览
简要总结
This is a randomized, double-masked, multicenter, study to evaluate the efficacy, safety, and tolerability of IRX-101 versus 5% povidone-iodine (PI) in subjects receiving intravitreal anti-VEGF injections. The study will be conducted in up to 30 centers in the United States (US).
详细描述
Intravitreal injection therapy (IVT) of anti-vascular endothelial growth factor (VEGF) agents has transformed the treatment landscape of several retinal diseases, including exudative (wet) macular degeneration, retinal vein occlusion, diabetic macular edema, and choroidal neovascularization. The most common adverse effects of IVT occur due to the side effects of Povidone-Iodine 5% (PI; brand name: Betadine® 5%; Alcon, Fort Worth, TX), the antiseptic placed on the ocular surface prior to each injection. PI is nearly universally used to prevent ocular infection (endophthalmitis). PI leads to marked corneal epithelial toxicity in humans,6, 7 resulting in debilitating side effects including decreased visual acuity and pain that can last more than 3 days post-IVT. Post-IVT pain is severe enough to require oral analgesics in up to 30% of patients and is a frequent cause of treatment discontinuation. Therefore, there is an unmet need in ophthalmology for a potent ocular antiseptic with a superior safety profile.
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
- Double (Participant, Care Provider)
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Capable of giving informed consent
- •Stated willingness to comply with all study procedures and availability for the duration of the study
- •Male or female, ≥ 18 years of age and receiving intravitreal anti-VEGF injections in one or both eyes
排除标准
- •Current or past diagnosis of endophthalmitis
- •Current diagnosis of uveitis
- •Current use of viscous lidocaine products for ocular anesthesia prior to IVT
- •Currently receiving intravitreal steroid injections
- •Concurrent participation in another clinical trial
研究组 & 干预措施
Test Drug
IRX-101 drops instilled prior to intravitreal injection
干预措施: IRX-101 (Drug)
Control
Povidone-Iodine/Betadine drops instilled prior to intravitreal injection
干预措施: Control (Drug)
结局指标
主要结局
Incidence of infectious endophthalmitis after topical use of IRX-101 combined with IVT
时间窗: 2 hours post-injection
To evaluate the rate of infectious endophthalmitis after topical use of IRX-101 following intravitreal injection therapy (IVT) (% occurrence or rate of population randomized to IRX-101 test arm)
次要结局
- Telephone questionnaire regarding patient-reported post-injection pain(2 hours post-injection)
