A Multicenter, Adaptive, Randomized Blinded Controlled Trial of the Safety and Efficacy of Investigational Therapeutics for the Treatment of COVID-19 in Hospitalized Adults (ACTT-4)
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 1,010
- 试验地点
- 72
- 主要终点
- The Proportion of Participants Not Meeting Criteria for One of the Following Two Ordinal Scale Categories at Any Time: 8) Death; 7) Hospitalized, on Invasive Mechanical Ventilation or Extracorporeal Membrane Oxygenation (ECMO)
研究概览
简要总结
ACTT-4 will evaluate the combination of baricitinib and remdesivir compared to dexamethasone and remdesivir. Subjects will be assessed daily while hospitalized. If the subjects are discharged from the hospital, they will have a study visit at Days 15, 22, and 29. For discharged subjects, it is preferred that the Day 15 and 29 visits are in person to obtain safety laboratory tests, oropharyngeal (OP) swabs, plasma (Day 29), and serum for secondary research as well as clinical outcome data. However, if infection control or other restrictions limit the ability of the subject to return to the clinic, these visits may be conducted by phone, and only clinical data will be obtained. The Day 22 visit does not have laboratory tests or collection of samples and is conducted by phone. The primary objective is to evaluate the clinical efficacy of baricitinib + remdesivir versus dexamethasone + remdesivir as assessed by the mechanical ventilation free survival by Day 29.
详细描述
This study is an adaptive randomized double-blind placebo-controlled trial to evaluate the safety and efficacy of novel therapeutic agents in hospitalized adults diagnosed with COVID-19. The study is a multicenter trial that will be conducted in up to approximately 100 sites globally. The study will compare different investigational therapeutic agents to a control arm. New arms can be introduced according to scientific and public health needs. There will be interim monitoring to allow early stopping for futility, efficacy, or safety. If one therapy proves to be efficacious, then this treatment may become the control arm for comparison(s) with new experimental treatment(s). Any such change would be accompanied by an updated sample size. This adaptive platform is used to rapidly evaluate different therapeutics in a population of those hospitalized with moderate to severe COVID-19. The platform will provide a common framework sharing a similar population, design, endpoints, and safety oversight. New stages with new therapeutics can be introduced. One independent Data and Safety Monitoring Board (DSMB) will actively monitor interim data in all stages to make recommendations about early study closure or changes to study arms.
ACTT-4 will evaluate the combination of baricitinib and remdesivir compared to dexamethasone and remdesivir. Subjects will be assessed daily while hospitalized. If the subjects are discharged from the hospital, they will have a study visit at Days 15, 22, and 29. For discharged subjects, it is preferred that the Day 15 and 29 visits are in person to obtain safety laboratory tests, oropharyngeal (OP) swabs, plasma (Day 29), and serum for secondary research as well as clinical outcome data. However, if infection control or other restrictions limit the ability of the subject to return to the clinic, these visits may be conducted by phone, and only clinical data will be obtained. The Day 22 visit does not have laboratory tests or collection of samples and is conducted by phone.
All subjects will undergo a series of efficacy, safety, and laboratory assessments. Safety laboratory tests and blood (serum and plasma) research samples and oropharyngeal (OP) swabs will be obtained on Days 1 (prior to infusion) and Days 3, 5, 8, and 11 (while hospitalized). OP swabs and blood (serum only) plus safety laboratory tests will be collected on Day 15 and 29 (if the subject attends an in-person visit or are still hospitalized).
The primary objective is to evaluate the clinical efficacy of baricitinib + remdesivir versus dexamethasone + remdesivir as assessed by the mechanical ventilation free survival by Day 29. The key secondary objective is to evaluate the clinical efficacy of baricitinib + remdesivir versus dexamethasone + remdesivir according to clinical status (8-point ordinal scale) at Day 15.
Contacts:
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
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 99 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Hospitalized with symptoms suggestive of COVID-
- •Subject (or legally authorized representative) provides informed consent prior to initiation of any study procedures and understands and agrees to comply with planned study procedures.
- •Male or non-pregnant female adult > / = 18 years of age at time of enrollment.
- •Illness of any duration and has laboratory-confirmed SARS-CoV-2 infection as determined by polymerase chain reaction (PCR) or other commercial or public health assay (e.g. NAAT, antigen test) in any respiratory specimen or saliva < / = 14 days prior to randomization.
- •Within the 7 days prior to randomization requiring new use of supplemental oxygen (or increased oxygen requirement if on chronic oxygen) and requires at the time of randomization low or high flow oxygen devices or use of non-invasive mechanical ventilation (ordinal scale category 5 or 6).
- •Women of childbearing potential must agree to either abstinence or use at least one primary form of contraception not including hormonal contraception from the time of screening through Day
- •Agrees not to participate in another blinded clinical trial (both pharmacologic and other types of interventions) for the treatment of COVID-19 through Day 29.
排除标准
- •Prior enrollment in ACTT-3 or ACTT-
- •Note: this includes subjects whose participation in ACTT was terminated early.
- •On invasive mechanical ventilation at the time of randomization (ordinal scale category 7).
- •Anticipated discharge from the hospital or transfer to another hospital which is not a study site within 72 hours of randomization.
- •Positive test for influenza virus during the current illness (influenza testing is not required by protocol).
- •Subjects with a low glomerular filtration rate (eGFR), specifically:
- •Subjects with an eGFR 15-30 mL/min are excluded unless in the opinion of the PI, the potential benefit of participation outweighs the potential risk of study participation.
- •All subjects with an eGFR <15 mL/min
- •All subjects on hemodialysis and/or hemofiltration at screening, irrespective of eGFR are excluded.
- •Neutropenia (absolute neutrophil count <700 cells/microliter, 0.7 x 10^3/microliter).
- •Lymphopenia (absolute lymphocyte count <200 cells/microliter, 0.20 x 10^3/microliter).
- •Received five or more doses of remdesivir including the loading dose, outside of the study as treatment for COVID-
- •Pregnancy or breast feeding (lactating women who agree to discard breast milk from Day 1 until two weeks after the last study product is given are not excluded).
- •Allergy to any study medication.
- •Received convalescent plasma or intravenous immunoglobulin [IVIg] for COVID-19, the current illness for which they are being enrolled.
- •Received any of the following in the two weeks prior to screening as treatment of COVID-19:
- •More than one dose of baricitinib for the treatment of COVID-19;
- •Other small molecule tyrosine kinase inhibitors (e.g. imatinib, gefitinib, acalabrutinib, etc.);
- •monoclonal antibodies targeting cytokines (e.g., TNF inhibitors, anti-interleukin-1 [IL-1], anti-IL-6 [tocilizumab or sarilumab], etc.);
- •monoclonal antibodies targeting T-cells or B-cells as treatment for COVID-
- •Note: receipt of anti-SARS-CoV-2 monoclonal antibody (mAb) prior to enrollment (e.g. bamlanivimab) for their current COVID-19 illness is not exclusionary
- •Use of probenecid that cannot be discontinued at study enrollment.
- •Received 6 mg or more of dexamethasone by mouth (po) or Intravenous (IV) (or equivalent for other glucocorticoids) in one day, on more than one day, in the 7 days prior to time of randomization. Note: 6 mg dexamethasone dose equivalents include 40 mg prednisone, 32 mg methylprednisolone and 160 mg hydrocortisone.
- •Received > / = 20 mg/day of prednisone po or IV (or equivalent for other glucocorticoids) for > / = 14 consecutive days in the 4 weeks prior to screening.
- •Have diagnosis of current active or latent tuberculosis (TB), if known, treated for less than 4 weeks with appropriate therapy (by history only, no screening required).
- •Serious infection (besides COVID-19), immunosuppressive state, or immunosuppressive medications that in the opinion of the investigator could constitute a risk when taking baricitinib or dexamethasone.
- •Have received any live vaccine (that is, live attenuated) within 4 weeks before screening, or intend to receive a live vaccine (or live attenuated) during the study. Note: Use of non-live (inactivated) vaccinations including SARS-CoV-2 vaccine is allowed for all subjects.
- •Had a known Venous thromboembolism (VTE)(deep vein thrombosis [DVT] or pulmonary embolism [PE]) during the current COVID-19 illness.
研究组 & 干预措施
Remdesivir plus Baricitinib
200 mg of remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of remdesivir while hospitalized for up to a 10-day total course; 4 mg of baricitinib administered as 2 tablets taken orally daily while hospitalized for up to a 14-day total course; and dexamethasone placebo administered as an intravenous injection daily while hospitalized for up to a 10-day total course.
干预措施: Baricitinib (Drug)
Remdesivir plus Baricitinib
200 mg of remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of remdesivir while hospitalized for up to a 10-day total course; 4 mg of baricitinib administered as 2 tablets taken orally daily while hospitalized for up to a 14-day total course; and dexamethasone placebo administered as an intravenous injection daily while hospitalized for up to a 10-day total course.
干预措施: Placebo (Other)
Remdesivir plus Baricitinib
200 mg of remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of remdesivir while hospitalized for up to a 10-day total course; 4 mg of baricitinib administered as 2 tablets taken orally daily while hospitalized for up to a 14-day total course; and dexamethasone placebo administered as an intravenous injection daily while hospitalized for up to a 10-day total course.
干预措施: Remdesivir (Drug)
Remdesivir plus Dexamethasone
200 mg of remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of remdesivir while hospitalized for up to a 10-day total course; baricitinib placebo administered as 2 tablets taken orally daily while hospitalized for up to a 14-day total course; and 6 mg of dexamethasone administered as an intravenous injection daily while hospitalized for up to a 10-day total course.
干预措施: Dexamethasone (Drug)
Remdesivir plus Dexamethasone
200 mg of remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of remdesivir while hospitalized for up to a 10-day total course; baricitinib placebo administered as 2 tablets taken orally daily while hospitalized for up to a 14-day total course; and 6 mg of dexamethasone administered as an intravenous injection daily while hospitalized for up to a 10-day total course.
干预措施: Placebo (Other)
Remdesivir plus Dexamethasone
200 mg of remdesivir administered intravenously on Day 1, followed by a 100 mg once-daily maintenance dose of remdesivir while hospitalized for up to a 10-day total course; baricitinib placebo administered as 2 tablets taken orally daily while hospitalized for up to a 14-day total course; and 6 mg of dexamethasone administered as an intravenous injection daily while hospitalized for up to a 10-day total course.
干预措施: Remdesivir (Drug)
结局指标
主要结局
The Proportion of Participants Not Meeting Criteria for One of the Following Two Ordinal Scale Categories at Any Time: 8) Death; 7) Hospitalized, on Invasive Mechanical Ventilation or Extracorporeal Membrane Oxygenation (ECMO)
时间窗: Day 1 through Day 29
Mechanical ventilation-free survival was assessed through Day 29, defined as the proportion of participants who had not died nor were hospitalized on invasive mechanical ventilation or ECMO as of Day 29. Results are reported as Kaplan Meier estimates.
The Proportion of Participants Not Meeting Criteria for One of the Following Two Ordinal Scale Categories at Any Time: 8) Death; 7) Hospitalized, on Invasive Mechanical Ventilation or Extracorporeal Membrane Oxygenation (ECMO) by Race
时间窗: Day 1 through Day 29
Mechanical ventilation-free survival was assessed through Day 29, defined as the proportion of participants who had not died nor were hospitalized on invasive mechanical ventilation or ECMO as of Day 29. Results are reported as Kaplan Meier estimates.
The Proportion of Participants Not Meeting Criteria for One of the Following Two Ordinal Scale Categories at Any Time: 8) Death; 7) Hospitalized, on Invasive Mechanical Ventilation or Extracorporeal Membrane Oxygenation (ECMO) by Ethnicity
时间窗: Day 1 through Day 29
Mechanical ventilation-free survival was assessed through Day 29, defined as the proportion of participants who had not died nor were hospitalized on invasive mechanical ventilation or ECMO as of Day 29. Results are reported as Kaplan Meier estimates.
The Proportion of Participants Not Meeting Criteria for One of the Following Two Ordinal Scale Categories at Any Time: 8) Death; 7) Hospitalized, on Invasive Mechanical Ventilation or Extracorporeal Membrane Oxygenation (ECMO) by Sex
时间窗: Day 1 through Day 29
Mechanical ventilation-free survival was assessed through Day 29, defined as the proportion of participants who had not died nor were hospitalized on invasive mechanical ventilation or ECMO as of Day 29. Results are reported as Kaplan Meier estimates.
次要结局
- Change From Baseline in Alanine Aminotransferase (ALT)(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Glucose(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Hemoglobin(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Prothrombin International Normalized Ratio (INR)(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Total Bilirubin(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Aspartate Aminotransferase (AST)(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Platelets(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in C-reactive Protein (CRP)(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Creatinine(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in White Blood Cell Count (WBC)(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in D-dimer Concentration(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Neutrophils(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Lymphocytes(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Monocytes(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Basophils(Days 1, 3, 5, 8, 11, 15 and 29)
- Change From Baseline in Eosinophils(Days 1, 3, 5, 8, 11, 15 and 29)
- Percentage of Participants Reporting Grade 3 and 4 Clinical and/or Laboratory Adverse Events (AEs)(Day 1 through Day 29)
- Percentage of Participants Reporting Serious Adverse Events (SAEs)(Day 1 through Day 29)
- Days of Invasive Mechanical Ventilation / Extracorporeal Membrane Oxygenation (ECMO)(Day 1 through Day 29)
- Days of Non-invasive Ventilation/High Flow Oxygen(Day 1 through Day 29)
- Duration of Supplemental Oxygen Use(Day 1 through Day 29)
- Desirability of Outcome Ranking (DOOR) at Day 15(Day 1 through Day 15)
- Desirability of Outcome Ranking (DOOR) at Day 29(Day 1 through Day 29)
- Duration of Hospitalization(Day 1 through Day 29)
- Number of Participants With Discontinuation or Temporary Suspension of Study Product Administration(Day 1 through Day 10)
- 14-day Participant Mortality(Day 1 through Day 15)
- 28-day Participant Mortality(Day 1 through Day 29)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 1(Day 1)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 3(Day 3)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 5(Day 5)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 8(Day 8)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 11(Day 11)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 15(Day 15)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 22(Day 22)
- Percentage of Participants at Each Clinical Status Using Ordinal Scale at Day 29(Day 29)
- Percentage of Participants Meeting Criteria for Each of the 8 Ordinal Scale Categories(Day 15)
- The Proportion of Participants Not Meeting Criteria for One of the Three Most Severe Ordinal Scale Categories at Any Time.(Day 1 through Day 29)
- Time to an Improvement of One Category From Baseline Using an Ordinal Scale(Day 1 through Day 29)
- Time to an Improvement of Two Categories From Baseline Using an Ordinal Scale(Day 1 through Day 29)
- Time to Recovery(Day 1 through Day 29)