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临床试验/NCT04377711
NCT04377711已完成3 期

A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety and Efficacy of Ciclesonide Metered-Dose Inhaler in Non-hospitalized Patients 12 Years of Age and Older With Symptomatic COVID-19 Infection

Covis Pharma S.à.r.l.1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2020年6月8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
已完成
发起方
入组人数
400
试验地点
1
主要终点
Time to Alleviation of COVID-19-related Symptoms by Day 30

研究概览

简要总结

The purpose of this study is to assess the safety and efficacy of Alvesco (ciclesonide) Inhalation Aerosol in non hospitalized patients with symptomatic COVID-19 infection in a multicenter, randomized, double-blind, placebo controlled study

详细描述

This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group, efficacy, and safety study of ciclesonide MDI for the treatment of symptomatic COVID-19 infection. Enrolled patients were male and female adults and adolescents 12 years of age or older with confirmed COVID-19 infection who were currently exhibiting symptoms of the disease and who were not currently hospitalized or under immediate consideration for hospitalization at the time of enrollment. The study consisted of an initial screening/enrollment/randomization visit, a 30-day treatment period, and a follow-up period.

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, Investigator)

盲法说明

Double Blind

入排标准

年龄范围
12 Years 至 100 Years(Child, 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

Group 1

Active Comparator

Participants receive Alvesco 320mcg, twice daily for 30 days via pMDI

干预措施: Ciclesonide (Drug)

Group 2

Placebo Comparator

Participants receive Placebo matching Alvesco , twice daily for 30 days via pMDI

干预措施: Placebo (Drug)

结局指标

主要结局

Time to Alleviation of COVID-19-related Symptoms by Day 30

时间窗: Day 30

Time to alleviation of COVID-19-related symptoms of cough, dyspnea, chills, feeling feverish, repeated shaking with chills, muscle pain, headache, sore throat, and new loss of taste or smell, defined as symptom-free for a continuous period of more than 24 hours (ie, later than 3 AM/PM assessments) by day 30

次要结局

  • Percentage of Patients With Subsequent Emergency Department Visit or Hospital Admission for Reasons Attributable to COVID-19 by Day 30(Day 30)
  • Percentage of Patients With Hospital Admission or Death by Day 30(Day 30)
  • All-cause Mortality by Day 30(Day 30)
  • COVID-19-related Mortality by Day 30(Day 30)
  • Percentage of Patients With Alleviation of COVID-19-related Symptoms Defined as Symptom-free for a Continuous Period of More Than 24 Hours (ie, Later Than 3 AM/PM Assessments) by Day 7, by Day 14, and by Day 30(By day 30)

研究者

发起方
Covis Pharma S.à.r.l.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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