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临床试验/EUCTR2021-006056-13-DE
EUCTR2021-006056-13-DE进行中(未招募)1 期

Open-Label, Uncontrolled, Single dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Safety of AZD7442 in Pediatric Participants Aged = 29 weeks Gestational Age to < 18 years - TRUST

AstraZeneca AB0 个研究点目标入组 100 人开始时间: 2022年3月28日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
100

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

  • Participant must be aged = 29 weeks to < 18 years of age.
  • Participant must weigh a minimum of 1.5 kg.
  • Increased risk of severe COVID-19 because of immunocompromised state or one or more comorbid conditions that increase the risk of severe COVID-19.
  • Medically stable (disease not requiring significant change in therapy or hospitalization for worsening disease during the one month prior to enrollment).
  • A negative RT-PCR test collected = 3 days before Day 1 or a negative rapid SARS-CoV-2 antigen test at screening.
  • No COVID-19 symptoms prior to enrollment within 10 days of dosing.
  • Increased risk for SARS-CoV-2 infection.
  • Increased risk of severe COVID-19 because of immunocompromised state or one or more comorbid conditions that increase the risk of severe COVID-19.
  • Medically stable (disease not requiring significant change in therapy or hospitalization for worsening disease during the one month prior to enrollment).
  • A positive RT-PCR test collected = 3 days before Day 1 or a positive rapid SARS-CoV-2 antigen test at screening.
  • Symptomatic participants must be dosed with IMP no more than 7 days from the self-reported date of first reported sign/symptom.
  • = 92% oxygen saturation at rest within 24 hours before Day 1 unless the participant is a regular receiver of chronic supplementary oxygen for a lung condition.
  • Participants hospitalized with COVID-19 between the onset of symptoms and dosing AZD7442 of = 7 days.
  • A positive RT-PCR test collected = 3 days before Day 1 or a positive rapid SARS-CoV-2 antigen test at screening.
  • Spontaneous blood Alanine Aminotransferase (ALT)/Aspartate Transaminase (AST) levels = 5 times the ULN.
  • Glomerular Filtration Rate (GFR) = 30 mL/min.
  • ROUTE OF ADMINISTRATION
  • - Participants will receive IM AZD7442 unless they meet any of the following criteria for IV
  • administration:
  • Severe COVID-19.
  • Contraindication of intramuscular (IM) dose due to thrombocytopenia, coagulation defects or any other condition that would compromise the absorption of AZD7442 or safety of the participant.
  • A central intravenous (IV) line.
  • Physician considers IV the appropriate route.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 100
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • MEDICAL CONDITIONS
  • Cohort 1: Significant infection or other acute illnesses including fever on or the day prior to or day of receiving AZD7442.
  • History of SARS-CoV-1 or Middle East Respiratory Syndrome Coronavirus (MERS-CoV).
  • Cohorts 1 and 2: Current need for immediate medical attention in an emergency room service or current need for hospitalization.
  • Mechanical ventilation or extracorporeal membrane oxygenation requirement for COVID-19.
  • History of allergic or reaction to any component of the study drug formulation.
  • History of hypersensitivity, injection/infusion-relation reactions or severe adverse reactions following administration of a mAb.
  • Co-morbidity requiring surgery within 7 days prior to study entry or is deemed life-threatening within 30 days prior to study entry.
  • THERAPY PRIOR ENROLLMENT
  • Prior receipt of convalescent COVID-19 plasma/sera or hyperimmune globulin therapy.
  • Prior receipt of mAb/biologic indicated for the prevention of SARS-CoV-2, treatment of COVID-19, or expected receipt during the period of study follow-up.
  • Prior receipt of a COVID-19 vaccine = 14 days before screening or plan to receive a COVID-19 vaccination = 14 days after IMP administration at study Visit 1.
  • History of alcohol or drug abuse within the past 2 years.
  • Vulnerable persons (ward of the state, kept in detention).

研究者

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