Charité Trial of Cenicriviroc (CVC) Treatment for COVID-19 Patients
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 入组人数
- 45
- 试验地点
- 1
- 主要终点
- Subject´s Responder status (score on the 7-point ordinal scale on Day 15)
研究概览
简要总结
The aim of this study is to test Cenicriviroc (CVC) as a means to reduce the severity of the lung disease COVID-19 caused by an infection with SARS-CoV-2. The safety of CVC, when administered to COVID-19 patients, will also be assessed. Furthermore, the clinical trial aims to answer the question of whether patients with pre-existing conditions, who have an increased risk of severe COVID-19 progression, benefit more and particularly from CVC. CVC is an orally available dual inhibitor of the chemokine receptors CCR2 and CCR5, which is expected to reduce (hyper-) inflammation in COVID-19.
The main goal of the study is to determine whether CVC helps increase the number of patients who are symptom-free and not hospitalized after 14 days compared to a placebo. Approximately 66.7% of the patients enrolled in the study will receive CVC and 33.3% will get an optically identical pill (placebo).
Subjects will be assessed daily while hospitalized. Discharged patients will be asked to attend study visits at Days 8, 15, 22, and 29 and 85. All subjects will undergo a series of clinical, safety, and laboratory assessments. Blood samples and oropharyngeal (OP) swabs will be obtained on Day 1; 3, 5 (while hospitalized); and Day 8, 15 and 29 (if able to return to clinic or still hospitalized). The presence of anti-SARS-CoV-2 antibodies will be determined on Days 29 and 85.
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
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subject provides written informed consent prior to initiation of any study procedures. Understands and agrees to comply with planned study procedures.
- •Male or non-pregnant female adult ≥18 years of age at time of enrolment.
- •Has laboratory-confirmed SARS-CoV-2 infection as determined by PCR and fulfils the case criteria of COVID-19 (One or more of the following must be met in lieu of a positive PCR test: fever [defined as a temperature ≥ 100.0°F / 37.8°C documented within 24 hr. of randomization] , absolute and relative lymphopenia and leukopenia, new typical infiltrates in x-ray of the chest or chest CT scan [only if obtained for clinical reasons; not required by study], no improvement on antibiotics).
- •Scoring a "3" or "4" (or "5", at the Investigator's discretion) on the 7-Point Ordinal Scale (see Outcome Measures) at enrolment. Note, if scoring a "2" at screening, inclusion will be met if the patient is in the process of being hospitalized or admitted to an inpatient setting. Such a patient would be assigned a "3" at enrolment for Baseline assessment purposes.
- •No participation in other clinical trials according to the German Medicines Act (AMG) (3 months before) at the time of this trial.
排除标准
- •ALT/AST > 5 times the upper limit of normal.
- •Patients with severe hepatic impairment (defined as liver cirrhosis Child stage B or C)
- •Stage 4 chronic kidney disease or requiring dialysis (i.e. eGFR < 30 ml/min)
- •Advanced cardiac (eg, severe heart failure [NYHA III-IV]) or pulmonary diseases which, in the Investigator's judgment, would not make participation appropriate.
- •Pregnancy or breast feeding.
- •Anticipated transfer to another hospital which is not a study site within 72 hours.
- •Known allergy or hypersensitivity to CVC or its components.
- •Use of medications that are contraindicated with CVC and that could not be replaced or stopped during the trial period
- •Administration of specified drugs which interfere with the metabolism of CVC.
- •Patients immediately or imminently requiring mechanical ventilation.
- •Patients unwilling to consent to saving and propagation of pseudonymised medical data for study reasons.
- •Subjects who are legally detained in an official institution.
- •Subjects that are unsuitable to understand or to comply with the study requirements in the opinion of the investigator.
- •Subjects who may be dependent on the sponsor, the investigator or the trial sites.
研究组 & 干预措施
Cenicriviroc (CVC)
Approximately 122 patients. Day 1: CVC 450 mg (300 mg AM; 150 mg PM; if patients receive their first dose on Day 1 past 2 PM, then their evening dose will be 300 mg and their next dose will be the following AM.) Days 2-28: CVC BID 150 mg (AM/PM). Every dose should be taken with food (within 30 min).
干预措施: Cenicriviroc (CVC) (Drug)
Placebo
Approximately 61 patients. A matching placebo will be given to the patients in the Placebo group at an equal volume and at the same schedule.
干预措施: Placebo (Drug)
结局指标
主要结局
Subject´s Responder status (score on the 7-point ordinal scale on Day 15)
时间窗: 14 days after enrollment (Day 15)
The Primary Endpoint will be the subject's responder status defined by achieving a score of "1" or "2" (discharged from hospital e.g.) on Day 15 on the following 7-point scale: 1. Not hospitalized, no limitations on activities; 2. Not hospitalized, limitation on activities; 3. Hospitalized, not requiring supplemental oxygen; 4. Hospitalized, requiring supplemental oxygen; 5. Hospitalized, on non-invasive ventilation or high-flow oxygen devices; 6. Hospitalized, on invasive mechanical ventilation or ECMO (Extracorporeal membrane oxygenation); 7. Death.
次要结局
- Evaluation of change in clinical condition based on the 7-point ordinal scale(day of enrollment and 15 days after enrollment)
- Evaluation of change in clinical condition based on the 7-point ordinal scale and Responder Status(day of enrollment, 8 days, 22 days and 29 days after enrollment)
- Hospital resource utilization comparison(29 days after enrollment, 85 days after enrollment)
研究者
Prof. Dr. med. Frank Tacke
Prof. Dr. med., PhD, MHBA
Charite University, Berlin, Germany