jRCT2051200159招募中不适用
A Randomized, Double Blind, Placebo Controlled Study to Evaluate the Safety and Efficacy of Aerosolized JH509 in Hospitalized Adult Patients with Mild to Moderate COVID 19
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- Genova Inc.
- 入组人数
- 385
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Double Blind
入排标准
- 年龄范围
- 20age old over 至 No limit(—)
- 性别
- All
入选标准
- •1.Written informed consent has been obtained from the participants with the age of over 20 years at the time of signing the informed consent.
- •2.SARS-CoV-2 infection is diagnosed by RT-PCR within 72 hours before starting drug administration.
- •3.Less than 6 days from onset of COVID-19 symptoms to starting the administration of the investigational drug. The symptoms are defined as one or more of the following: fever (37.5 or higher), respiratory symptoms (cough, shortness of breath, chest pain, sore throat, running nose, nasal congestion, etc.), headache, malaise, abdominal pain, diarrhea, nausea, vomiting, loss of smell, loss of taste, or other COVID-19 symptoms defined by investigators or physicians.
- •4.Have at least one of the following findings.
- •Oxygen saturation (SpO2) measured by pulse oximeter is less than 96% but more than 93%.
- •Chest X-ray or CT scan shows pneumonia findings suggestive of COVID-19 infection
排除标准
- •History of hypersensitivity to interferon or Novaferon or any excipients of interferon or Novaferon.
- •Having received other antiviral treatments (Favipiravir, Remdesivir, interferon, etc.)
- •CTCAE Grade 3 or higher liver dysfunction (ALT / AST> 5ULN) or renal dysfunction (eGFR <30 mL / min / 1.73 m2)
- •Active infections or other medical conditions that contraindicate inhalation therapy
结局指标
主要结局
-
Time to clinical improvement by two points on a 7-point ordinal scale
次要结局
- Rate of clinical improvement by at least 1point on a 7-point ordinal scale(Day1 to Day10, Day14, and Day28)
- Rate of clinical deterioration by at least 1 point on a 7-point ordinal scale(Day1 to Day10, Day14, and Day28)
- Time to negative RT-PCR testofSARS-CoV-2 in nasopharyngeal swap or in other samples from respiratory system
- Rate of negative RT-PCR testofSARS-CoV-2 in nasopharyngeal swap or in other samples from respiratory system
- Post-baseline changes of SARS-CoV-2viral loads in nasopharyngeal swap or in other samples from respiratory system
- Rate of mortality(Day 28)
- Duration of hospital stay for treatment of new coronavirus infection
- Time to resolution of symptoms defined as a (National Early Warning Score 2) NEWS2 of 0 maintained for 24hours
- Rate and duration of requiring supplemental oxygen
- Rate and duration of requiring mechanical ventilator (invasive or non-invasive)
- Rate of alive patients without using invasive ventilator or ECMO(Day 28)
- Adverse events
研究者
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A Randomized, Double Blind, Placebo Controlled Study to Evaluate the Safety and Efficacy of Aerosolized JH509 in Hospitalized Adult Patients with Mild to Moderate COVID 19COVID-19 infections diseaseJPRN-jRCT2051200159Shoji Hashimoto385
