跳至主要内容
临床试验/NCT05127525
NCT05127525终止3 期

Randomized, Double-Masked, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of IRX-101 Versus 5% Povidone-Iodine as an Ocular Surface Sterilizer

iRenix Medical, Inc.1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2021年11月15日最近更新:
适应症
干预措施
相关药物

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

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

Experimental

IRX-101 drops instilled prior to intravitreal injection

干预措施: IRX-101 (Drug)

Control

Active Comparator

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)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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