跳至主要内容
临床试验/NCT02265393
NCT02265393已完成2 期

A 6-Month, Prospective, Randomized, Multicenter, Placebo-Controlled Safety Study of OTO-104 Given at 3-Month Intervals by Intratympanic Injection in Subjects With Unilateral Meniere's Disease Followed by a 6-Month Open-Label Extension

Otonomy, Inc.15 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2014年10月最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
Otonomy, Inc.
入组人数
128
试验地点
15
主要终点
Safety

研究概览

简要总结

This is a 2-part study of OTO-104 in subjects with unilateral Meniere's disease in the United Kingdom. The first part is a randomized, placebo-controlled study comparing the safety profile of 2 injections of OTO-104 or placebo spaced 3 months apart. The second part is an open-label extension where all subjects will receive an additional 2 intratympanic injections of OTO-104 spaced 3 months apart. Each subject will participate on the study for a total of 1 year.

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, 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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

OTO-104

Active Comparator

12 mg OTO-104 (dexamethasone)

干预措施: OTO-104 (Drug)

Placebo

Placebo Comparator

OTO-104 vehicle

干预措施: Placebo (Drug)

结局指标

主要结局

Safety

时间窗: Up to 1 Year

Otoscopy, audiometry, tympanometry, adverse events

次要结局

  • Meniere's Symptom Questionnaire(Up to 1 Year)

研究者

发起方
Otonomy, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (15)

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