Tocilizumab to Prevent Clinical Decompensation in Hospitalized, Non-critically Ill Patients With COVID-19 Pneumonitis

University of Chicago32 enrolled

Overview

Coronavirus disease-2019 (COVID-19) has a quoted inpatient mortality as high as 25%. This high mortality may be driven by hyperinflammation resembling cytokine release syndrome (CRS), offering the hope that therapies targeting the interleukin-6 (IL-6) axis therapies commonly used to treat CRS can be used to reduce COVID-19 mortality. Retrospective analysis of severe to critical COVID-19 patients receiving tocilizumab demonstrated that the majority of patients had rapid resolution (i.e., within 24-72 hours following administration) of both clinical and biochemical signs (fever and CRP, respectively) of hyperinflammation with only a single tocilizumab dose. Hypotheses: 1. Tocilizumab is effective in decreasing signs, symptoms, and laboratory evidence of COVID-19 pneumonitis in hospitalized, non-critically ill patients with clinical risk factors for clinical decompensation, intensive care utilization, and death. 2. Low-dose tocilizumab is effective in decreasing signs, symptoms, and laboratory evidence of COVID-19 pneumonitis in hospitalized, non-critically ill patients with and without clinical risk factors for clinical decompensation, intensive care utilization, and death. Objectives: 1. To establish proof of concept that tocilizumab is effective in decreasing signs, symptoms, and laboratory evidence of COVID-19 pneumonitis in hospitalized, non-critically ill patients with clinical risk factors for clinical decompensation, intensive care utilization, and death, as determined by the clinical outcome of resolution of fever and the biochemical outcome measures of time to CRP normalization for the individual patient and the rate of patients whose CRP normalize. 2. To establish proof of concept that low-dose tocilizumab is effective in decreasing signs, symptoms, and laboratory evidence of COVID-19 pneumonitis in hospitalized, non-critically ill patients without clinical risk factors for clinical decompensation, intensive care utilization, and death, as determined by the clinical outcome of resolution of fever and the biochemical outcome measures of time to CRP normalization for the individual patient and the rate of patients whose CRP normalize.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Interventions

TocilizumabDRUG

Group A: Tocilizumab (beginning dose 200mg) Single dose is provisioned, patient is eligible to receive up to two doses, with re-evaluation of clinical and biochemical responses performed every 24 hours. Second dose is provisioned if: 1. Increasing supplemental oxygen requirement or Tmax higher than baseline in the 24h following initial tocilizumab administration AND 2. CRP decrease is \< 25% at 24 hours following tocilizumab administration and CRP \> 40mg/L

TocilizumabDRUG

Group B: Low-dose tocilizumab (beginning dose 80mg) Single dose is provisioned, patient is eligible to receive up to two doses, with re-evaluation of clinical and biochemical responses performed every 24 hours. Second dose is provisioned if: 1. Increasing supplemental oxygen requirement or Tmax higher than baseline in the 24h following initial tocilizumab administration AND 2. CRP decrease is \< 25% at 24 hours following tocilizumab administration and CRP \> 40mg/L

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Adults ≥ 18 years of age * Approval from the patient's primary service * Admitted as an inpatient to University of Chicago Medicine * Fever, documented in electronic medical record and defined as: T ≥ 38\*C by any conventional clinical method (forehead, tympanic, oral, axillary, rectal) * Positive test for active SARS-CoV-2 infection * Radiographic evidence of infiltrates on chest radiograph (CXR) or computed tomography (CT) * Ability to provide written informed consent on the part of the subject or, in the absence of decisional capacity of the subject, an appropriate surrogate (e.g. a legally authorized representative). Exclusion Criteria: * Concurrent use of invasive mechanical ventilation (patients receiving non-invasive mechanical ventilation \[CPAP, BiPap, HHFNC\] are eligible) * Concurrent use of vasopressor or inotropic medications * Previous receipt of tocilizumab or another anti-IL6R or IL-6 inhibitor. * Known history of hypersensitivity to tocilizumab. * Patients who are actively being considered for a study of an antiviral agent that would potentially exclude concurrent enrollment on this study. * Patients actively receiving an investigational antiviral agent in the context of a clinical research study. * Diagnosis of end-stage liver disease or listed for liver transplant. * Elevation of AST or ALT in excess of 5 times the upper limit of normal. * Neutropenia (Absolute neutrophil count \< 500/uL). * Thrombocytopenia (Platelets \< 50,000/uL). * On active therapy with a biologic immunosuppressive agent, which include the following biologics and any biosimilar versions thereof: * Alemtuzumab * Blinatumomab * Brentuximab * Daratumumab * Elotuzumab * Ibritumomab * Obinutuzumab * Ofatumumab * Ocrelizumab * Rituximab * Inotuzumab * Gemtuzumab * Tositumumab * Moxetumomab * Polatuzumab * Abatacept * Adalimumab * Belimumab * Certolizumab * Eculizumab * Etanercept * Golimumab * Infliximab * Ixekizumab * Rituximab * Sarilumab * Secukinumab * Tocilizumab * Ustekinumab * On active therapy with a JAK2-targeted agent, which include the following: * Tofacitinib * Baricitinib * Upadacitinib * Ruxolitinib * History of bone marrow transplantation or solid organ transplant. * Known history of Hepatitis B or Hepatitis C. * Known history of mycobacterium tuberculosis infection at risk for reactivation. * Known history of gastrointestinal perforation or active diverticulitis. * Multi-organ failure as determined by primary treating team * Any other documented serious, active infection besides COVID-19. * Pregnant patients * Patients who are unable to discontinue scheduled antipyretic medications, either as monotherapy (e.g., acetaminophen or ibuprofen \[aspirin is acceptable\]) or as part of combination therapy (e.g., hydrocodone/acetaminophen, aspirin/acetaminophen/caffeine \[Excedrin®\]) * CRP \< 40 mg/L (or ug/mL) Patients will be assigned to Group A if: ● C-reactive protein (CRP) ≥ 75 ug/mL AND Any one of the following criteria are met: * Previous ICU admission * Previous non-elective intubation * Admission for heart failure exacerbation within the past 12 months * History of percutaneous coronary intervention (PCI) * History of coronary artery bypass graft (CABG) surgery * Diagnosis of pulmonary hypertension * Baseline requirement for supplemental O2 * Diagnosis of interstitial lung disease (ILD) * Admission for chronic obstructive pulmonary disease (COPD) exacerbation within the past 12 months * Asthma with use of daily inhaled corticosteroid * History of pneumonectomy or lobectomy * History of radiation therapy to the lung * History of HIV * Cancer of any stage and receiving active treatment (excluding hormonal therapy) * Any history of diagnosed immunodeficiency * End-stage renal disease (ESRD) requiring peritoneal or hemodialysis * History of cerebrovascular accident with residual, patient-reported neurologic deficit * BMI \>30 kg/m2 * Supplemental O2 requirement \> 6L in the 24 hours prior to enrollment and tocilizumab administration All other eligible patients assigned to Group B

Outcomes

Primary Outcomes

Number of Participants With Clinical Response in Maximum Temperature (Tmax)

Number of Participants with Clinical Response in Maximum Temperature (Tmax)

Time frame: Assessed for the 24 hour period after tocilizumab administration

Number of Participants With Biochemical Response as Determined by CRP Response

Number of Participants with Biochemical Response as determined by CRP Response. Defined as at least 25% decrease in CRP from baseline at least 16 hours after administration of drug.

Time frame: Assessed every 24 hours during patient's hospitalization, up to 4 weeks after tocilizumab administration

Secondary Outcomes

Overall Survival

28-Day Overall Survival is defined as the status of the patient at the end of 28 days, beginning from the time of the first dose of tocilizumab.

Time frame: 28 days

Survival to Hospital Discharge

This will be defined as the percentage of patients who are discharged in stable condition compared to the percentage of patients who die in the hospital. Patients who are discharged to hospice will be excluded from this calculation.