CoVPN 3002 A Phase III Randomized, Double-blind, Placebo-controlled Multicenter Study in Adults to Determine the Safety, Efficacy, and Immunogenicity of AZD1222 for the Prevention of COVID-19 LC2

CoVPN 3002 一项针对成人的 III 期随机、双盲、安慰剂对照多中心研究，以确定 AZD1222 预防 COVID-19 LC2 的安全性、有效性和免疫原性

• 批准号: 10570741
• 负责人: Margaret Juliana McElrath
• 金额: $ 53.2万
• 依托单位: FRED HUTCHINSON CANCER CENTER
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-06-29 至 2023-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10570741
• 关键词: 18 year old; 2019-nCoV; Address; Adenoviruses; Adult; Age-Years; Antibody Response; Antigens; AstraZeneca COVID-19 vaccine; Binding; Biological Assay; Biometry; COVID-19; COVID-19 Prevention Network; COVID-19 outbreak; COVID-19 pandemic; COVID-19 prevention; COVID-19 screening; COVID-19 severity; COVID-19 vaccine; Cellular Assay; Clinical; Clinical Trials; Clinical Trials Network; Cohort Studies; Communicable Diseases; Constitution; Country; Data Analytics; Development; Diagnosis; Disease; Dose; Double-Blind Method; Emergency department visit; End Point Assay; Eye; Future; Goals; HIV Vaccine Trials Network; HIV vaccine; Health; Hospitalization; Immune; Immune response; Immunity; Immunologic Monitoring; Immunology; Individual; Infection; Infection Control; Infection prevention; Injections; International; Intervention; Knowledge; Laboratories; Lead; Leadership; Malaria; Mediating; Membrane Glycoproteins; Monitor; Morbidity - disease rate; Multicenter Studies; Pan Genus; Participant; Persons; Phase; Physicians; Placebo Control; Placebos; Population; Preparation; Prevention; Preventive; Protocols documentation; Quality Control; Randomized; Randomized Clinical Trials; Recombinants; Research Methodology; Risk; SARS-CoV-2 infection; SARS-CoV-2 spike protein; Safety; Sampling; Scientist; Serology test; Serum; Site; System; Testing; Therapeutic Monoclonal Antibodies; Typhoid Fever; United States; United States National Institutes of Health; Vaccines; Validation; adaptive immune response; base; clinical trial analysis; design; efficacy study; efficacy testing; efficacy trial; experience; high risk; immune function; immunogenicity; improved; mortality; neutralizing antibody; operation; prevent; programs; quality assurance; racial and ethnic; racial diversity; rational design; recruit; remote monitoring; response; severe COVID-19; symptomatic COVID-19; vaccine trial; vector vaccine

This proposal outlines the scientific agenda for the COVID-19 Prevention Network (CoVPN) Vaccines Leadership Operations Center (LOC) for implementation of the first COVID-19 vaccine efficacy trial “A Phase III Randomized, Double-blind, Placebo-controlled Multicenter Study in Adults to Determine the Safety, Efficacy, and Immunogenicity of AZD1222, A Non-replicating ChAdOx1 Vector Vaccine, for the Prevention of COVID- 19.” With the global COVID-19 pandemic, we recognize a significant need for vaccines that modify COVID-19 in SARS-CoV-2 infected individuals. Addressing this gap, the National Institute of Health (NIH) led rapid constitution of the CoVPN, partnering 5 NIH supported clinical trial networks, to create an enhanced network of physician scientists at 64 United States (US) and 55 international clinical trial sites in 15 countries dedicated to developing globally effective vaccines for SARS-CoV-2. Due to its extensive experience implementing global HIV vaccine trials over the last 20 years, the HIV Vaccine Trials Network (HVTN) LOC was selected as the LOC for CoVPN vaccine trials. This trial, a phase 3, placebo-controlled, double-blinded study will test the efficacy of AZD1222, a recombinant replication-defective chimpanzee adenovirus expressing the SARS-CoV-2 spike (S) surface glycoprotein, to modify COVID-19 disease in adults 18 year of age and older. Participants will be recruited from up to 100 clinical trial sites across the US, using data analytics to target high risk individuals with a diverse racial and ethnic profile. Participants will receive symptomatic screening for SARS-CoV-2 infection, and if they become infected will be monitored with frequent clinical check-ins and remote monitoring of vital signs. Infected individuals who progress to moderate-severe COVID-19 will be referred for hospitalization. All trial endpoint assays will be done at CoVPN laboratories, using qualified and validated assays for diagnosis and immune monitoring. Specific aims of this study are to demonstrate efficacy of AZD1222 to prevent COVID-19, to evaluate the safety, tolerability and reactogenicity of 2 injections given 4 weeks apart, to assess the ability to prevent infection with SARS-CoV-2, to assess the ability to modify COVID-19 disease, to assess the ability to prevent emergency room visits, and to evaluate the binding and neutralizing antibody responses. This efficacy trial will tell us much about the adaptive immune response in persons who receive a SARS-CoV-2 S protein based vaccine and about their ability to modify the disease course of COVID-19. In addition, it will improve our understanding of the dynamics and duration of these responses and will inform rational design and testing of preventive and therapeutic monoclonal antibody interventions. Lastly, the results of this trial will be used to assess registration of this vaccine product as well as to modify future COVID-19 vaccine trials planned over the next 12 months.

该提案概述了COVID-19预防网络（CoVPN）疫苗的科学议程 领导运营中心（COVID-19疫苗有效性试验“A阶段”）的实施 III.在成人中进行的随机、双盲、安慰剂对照、多中心研究，以确定安全性、疗效、 AZD 1222（一种非复制型ChAdOx 1载体疫苗）用于预防COVID-1的免疫原性 十九岁。" 随着全球COVID-19大流行，我们认识到对修饰COVID-19的疫苗的巨大需求， SARS-CoV-2感染者。为了解决这一差距，美国国家卫生研究院（NIH）迅速 CoVPN的组成，与5个NIH支持的临床试验网络合作，以创建一个增强的网络， 美国64家临床试验机构和15个国家的55家国际临床试验机构的医生科学家致力于 研发全球有效的SARS-CoV-2疫苗。由于其在实施全球 在过去20年的艾滋病毒疫苗试验中，艾滋病毒疫苗试验网络（HVTN）被选为 用于CoVPN疫苗试验。 本试验是一项III期、安慰剂对照、双盲研究，将检测AZD 1222（一种重组 表达SARS-CoV-2刺突（S）表面糖蛋白的复制缺陷型黑猩猩腺病毒， 在18岁及以上的成年人中改变COVID-19疾病。参与者将从最多100人中招募 美国各地的临床试验站点，使用数据分析针对具有不同种族和 种族特征 参与者将接受SARS-CoV-2感染的症状筛查，如果他们被感染， 通过频繁的临床检查和远程监测生命体征进行监测。受感染的人， 发展至中重度COVID-19将被转介住院。所有试验终点测定均将 在CoVPN实验室完成，使用合格和经验证的检测方法进行诊断和免疫监测。 本研究的具体目的是证明AZD 1222预防COVID-19的有效性，评估 间隔4周进行2次注射的安全性、耐受性和反应原性，以评估预防 SARS-CoV-2感染，评估改变COVID-19疾病的能力，评估预防 急诊室就诊，并评估结合和中和抗体应答。这项疗效试验将 告诉我们很多关于接受基于SARS-CoV-2S蛋白的人的适应性免疫反应的信息， 疫苗以及它们改变COVID-19病程的能力。此外，它还将改善我们的 了解这些响应的动态和持续时间，并将为合理设计和测试提供信息， 预防性和治疗性单克隆抗体干预。最后，这项试验的结果将用于 评估该疫苗产品的注册情况，并修改未来计划在2019年进行的COVID-19疫苗试验。 未来12个月