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临床试验/NCT03511066
NCT03511066终止2 期

A Phase IIb, Randomized, Double-blind, Multicenter, Placebo-controlled Study Evaluating the Efficacy and Safety of CT-P27 in Subjects With Acute Uncomplicated Influenza A Infection

Celltrion1 个研究点 分布在 1 个国家目标入组 228 人开始时间: 2016年12月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
Celltrion
入组人数
228
试验地点
1
主要终点
Time to Resolution of Influenza Symptoms and Fever

研究概览

简要总结

This study is a Phase IIb, Randomized, Double-blind, Multicenter, Placebo-controlled study evaluating the efficacy and safety of CT-P27 in subjects with acute uncomplicated influenza A infection.

详细描述

This study is a Phase IIb, Randomized, Double-blind, Multicenter, Placebo-controlled study. All enrolled subjects will be given a single dose of 90 mg/kg CT-P27, 45 mg/kg CT-P27, or placebo intravenously over 90 minutes (±15 minutes) on Day 1 and then followed by Day 110.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
19 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male or Female subjects between the ages of 19 and 64 years, both inclusive
  • Diagnosed with influenza A at screening using rapid influenza diagnostic test
  • Onset of influenza symptoms and fever is within 48 hours at screening
  • At least 2 of symptoms (moderate to severe in intensity)
  • ≥38.0'C body temperature at screening

排除标准

  • Taking antiviral treatment for influenza or has a history of using these antivirals within 14 days prior to the administration of study drug
  • Positive influenza B or A+B infection

研究组 & 干预措施

CT-P27 90 mg/kg

Experimental

CT-P27 will be administrated once in IV infusion.

干预措施: CT-P27 90 mg/kg (Drug)

CT-P27 45mg/kg

Experimental

CT-P27 will be administrated once in IV infusion.

干预措施: CT-P27 45 mg/kg (Drug)

Placebo

Placebo Comparator

Placebo will be administrated once in IV infusion.

干预措施: Placebo (Drug)

结局指标

主要结局

Time to Resolution of Influenza Symptoms and Fever

时间窗: Twice a day (Morning and Evening) from Day 1 to Day 8

Time to resolution of influenza symptoms (cough, sore throat, nasal congestion, headache, feeling feverish, body aches and pains, and fatigue) and fever (\<37.8)

次要结局

未报告次要终点

研究者

发起方
Celltrion
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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