跳至主要内容
临床试验/EUCTR2020-001784-88-FI
EUCTR2020-001784-88-FI进行中(未招募)1 期

WHO SOLIDARITY Finland: The multicenter trial on the efficacy of different anti-viral drugs in SARS-CoV-2 infected patients (COVID-19) - SOLIDARITY Finland

niversity of Helsinki0 个研究点目标入组 582 人开始时间: 2020年4月17日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
582

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Adult patients, 18 years and above
  • 2. Confirmed SARS-2-CoV-2 infection by PCR
  • 3. Admitted to the hospital ward or the ICU
  • 4. Subjects (or legally authorized representative) provides written
  • informed consent prior to initiation of the study
  • 5. No anticipated transfer within 72 hours to a non-study hospital
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 291
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 291

排除标准

  • 1.Severe co-morbidity with life expectancy <3 months according to investigators assessment
  • 2.ASAT/ALAT > 5 times the upper limit of normal
  • 3.Acute co-morbidity within 7 days before inclusion such as myocardial infarction or UAP (not including troponin elevation due to infection)
  • 4.Known intolerance to the available study drugs
  • 5.Pregnancy or breast feeding
  • 6.Any reason why, in the opinion of the investigators, the patient should not participate
  • 7.Subject participates in a potentially confounding drug or device trial during the course of the study
  • 8.Already receiving any of the study drugs
  • 9.Renal failure (eGRF < 30 mL/min) or dialysis or continuous veno-venous hemofiltration

研究者

发起方
niversity of Helsinki

相似试验

进行中(未招募)
1 期
A clinical study to evaluate the efficacy of different anti-viral drugs in SARS-CoV-2 infected patients (COVID-19).SARS-COV-2 infectionMedDRA version: 21.1Level: LLTClassification code 10037373Term: Pulmonary disorderSystem Organ Class: 100000004855
EUCTR2020-000982-18-SEKarolinska University hospital1,218
进行中(未招募)
不适用
Multi-center, Multi-national Clinical Trial of the Application of Tissue Repair Cell (TRC) Therapy of Osteonecrosis in the Femur Head
EUCTR2006-001286-42-ESAastrom Biosciences, Inc15
进行中(未招募)
1 期
Trial of efficacy and safety of tisotumab vedotin (HuMax®-TF-ADC) in patients with previously treated, advanced cervical cancerrecurrent or metastatic cervical cancerMedDRA version: 21.1Level: PTClassification code 10008342Term: Cervix carcinomaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2017-003413-25-CZGenmab A/S100
进行中(未招募)
1 期
Trial of efficacy and safety of tisotumab vedotin (HuMax®-TF-ADC) in patients with previously treated, advanced cervical cancerrecurrent or metastatic cervical cancerMedDRA version: 21.1Level: PTClassification code 10008342Term: Cervix carcinomaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2017-003413-25-DKGenmab A/S100
进行中(未招募)
1 期
Trial of efficacy and safety of tisotumab vedotin (HuMax®-TF-ADC) in patients with previously treated, advanced cervical cancerrecurrent or metastatic cervical cancerMedDRA version: 20.0Level: PTClassification code 10008342Term: Cervix carcinomaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2017-003413-25-ESGenmab A/S100