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CORIMUNO-19 - Tocilizumab Trial - TOCI (CORIMUNO-TOCI)

Cohort Multiple Randomized Controlled Trials Open-label of Immune Modulatory Drugs and Other Treatments in COVID-19 Patients - Tocilizumab Trial - CORIMUNO-19 - TOCI (CORIMUNO-TOCI)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04331808
Acronym
CORIMUNO-TOC
Enrollment
228
Registered
2020-04-02
Start date
2020-03-30
Completion date
2020-11-09
Last updated
2025-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corona Virus Infection

Brief summary

The overall objective of the study is to determine the therapeutic effect and tolerance of Tocilizumab in patients with moderate, severe pneumonia or critical pneumonia associated with Coronavirus disease 2019 (COVID-19). Tocilizumab (TCZ) is an anti-human IL-6 receptor monoclonal antibody that inhibits signal transduction by binding sIL-6R and mIL-6R. The study has a cohort multiple Randomized Controlled Trials (cmRCT) design. Randomization will occur prior to offering Tocilizumab administration to patients enrolled in the CORIMUNO-19 cohort. Tocilizumab will be administered to consenting adult patients hospitalized with CORVID-19 either diagnosed with moderate or severe pneumonia requiring no mechanical ventilation or critical pneumonia requiring mechanical ventilation. Patients who will chose not to receive Tocilizumab will receive standard of cares. Outcomes of Tocilizumab-treated patients will be compared with outcomes of standard of care treated patients as well as outcomes of patients treated with other immune modulators.

Interventions

DRUGTocilizumab

Tocilizumab 8mg/kg on day 1 and if no response (no decrease of oxygen requirement) a second injection at day 3 (fixed dose of 400 mg)

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients included in the CORIMUNO-19 cohort 2. Patients belonging to one of the 2 following groups: * Group 1: Cases meeting all of the following criteria * Requiring more than 3L/min of oxygen * OMS/WHO progression scale = 5 * No Non Invasive Ventilation or High flow * Group 2: Cases meeting all of the following criteria * Respiratory failure AND (requiring mechanical ventilation OR Non Invasive Ventilation OR High flow) * WHO progression scale \>=6 * No do-not-resuscitate order (DNR order)

Exclusion criteria

* Patients with

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Participants With WHO Clinical Progression Scale > 5 at Day 4 -- Severe COVID Population (WHO Clinical Progression Scale =5 at Baseline)4 daysPercentage of participants who has died or needed non-invasive or mechanical ventilation by day 4 (WHO clinical progression scale \> 5). A patient with new do-not-resuscitate order at day 4 will be considered as with a score \> 5. WHO progression scale: Uninfected; non viral RNA detected: 0 Asymptomatic; viral RNA detected: 1 Symptomatic; Independent: 2 Symptomatic; Assistance needed: 3 Hospitalized; No oxygen therapy: 4 Hospitalized; oxygen by mask or nasal prongs: 5 Hospitalized; oxygen by NIV or High flow: 6 Intubation and Mechanical ventilation, pO2/FIO2\>=150 OR SpO2/FIO2\>=200: 7 Mechanical ventilation, (pO2/FIO2\<150 OR SpO2/FIO2\<200) OR vasopressors (norepinephrine \>0.3 microg/kg/min): 8 Mechanical ventilation, pO2/FIO2\<150 AND vasopressors (norepinephrine \>0.3 microg/kg/min), OR Dialysis OR ECMO: 9 Dead: 10
Percentage of Participants With Non-invasive Ventilation, Mechanical Ventilation or Death at Day 14 (WHO Clinical Progression Scale =5 at Baseline)Day 1 to Day 14Survival without needs of ventilator utilization (including non invasive ventilation and high flow) at day 14. Percentage of non-invasive ventilation, mechanical ventilation or death. Thus, events considered are needing ventilator utilization (mechanical or non-invasive ventilation including high flow oxygen), or death. New do-not-resuscitate (DNR) order (if given after the inclusion of the patient) will be considered as an event at the date of the DNR.
Percentage of Participants With no Improvement in WHO Clinical Progression Scale at Day 4 -- Critical COVID Population ( WHO Clinical Progression Scale >5 at Baseline)4 daysResults are presented as the percentage not improved, so that an effective treatment would be associated with a decrease in percentage WHO progression scale: Uninfected; non viral RNA detected: 0 Asymptomatic; viral RNA detected: 1 Symptomatic; Independent: 2 Symptomatic; Assistance needed: 3 Hospitalized; No oxygen therapy: 4 Hospitalized; oxygen by mask or nasal prongs: 5 Hospitalized; oxygen by NIV or High flow: 6 Intubation and Mechanical ventilation, pO2/FIO2\>=150 OR SpO2/FIO2\>=200: 7 Mechanical ventilation, (pO2/FIO2\<150 OR SpO2/FIO2\<200) OR vasopressors (norepinephrine \>0.3 microg/kg/min): 8 Mechanical ventilation, pO2/FIO2\<150 AND vasopressors (norepinephrine \>0.3 microg/kg/min), OR Dialysis OR ECMO: 9 Dead: 10
Cumulative Incidence (Percentage of Participants) With Successful Tracheal Extubation at Day 14 -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 1 to Day 14Cumulative incidence of successful tracheal extubation (defined as duration extubation \> 48h) at day 14 if patients have been intubated before day 14 ; or removal of Non Invasive Ventilation or high flow (for \> 48h) if they were included under oxygen by Non Invasive Ventilation or High flow (score 6) and remained without intubation. Death or new do-not-resuscitate order (if given after the inclusion of the patient) will be considered as a competing event.

Secondary

MeasureTime frameDescription
Cumulative Incidence (Percentage of Participants) of Discharge From Hospital28, 90 daysTime to discharge from hospital
Percentage of Participants Surviving (Overall Survival)14, 28 and 90 daysPercentage of participants surviving at 14, 28 and 90 days
PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)day 1 to day 14Evolution of PaO2/FiO2 ratio PaO2 is partial pressure of arterial oxygen expressed in mmHg. FiO2 is fraction of inspired oxygen (for instance, 0.33 for 33% oxygen) with no units. PaO2/FiO2 ratio is expressed in mmHg.
Cumulative Incidence (Percentage of Participants) of Intensive Care Unit Discharge -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)28, 90 daysTime to discharge from Intensive Care Unit
WHO Progression Scale4, 7 and 14 daysWHO progression scale: Uninfected; non viral RNA detected: 0 Asymptomatic; viral RNA detected: 1 Symptomatic; Independent: 2 Symptomatic; Assistance needed: 3 Hospitalized; No oxygen therapy: 4 Hospitalized; oxygen by mask or nasal prongs: 5 Hospitalized; oxygen by NIV or High flow: 6 Intubation and Mechanical ventilation, pO2/FIO2\>=150 OR SpO2/FIO2\>=200: 7 Mechanical ventilation, (pO2/FIO2\<150 OR SpO2/FIO2\<200) OR vasopressors (norepinephrine \>0.3 microg/kg/min): 8 Mechanical ventilation, pO2/FIO2\<150 AND vasopressors (norepinephrine \>0.3 microg/kg/min), OR Dialysis OR ECMO: 9 Dead: 10
Mean of Ventilator Free-days at Day 28 -- Critical COVID Population (WHO-clinical Progression Scale >5 at Baseline)28 days28-day ventilator free-days
Cumulative Incidence (Percentage of Participants) of Oxygen Supply IndependencyDay 28, 90Time to oxygen supply independency

Countries

France

Participant flow

Participants by arm

ArmCount
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)
Tocilizumab 8mg/kg on day 1 and if no response (no decrease of oxygen requirement) a second injection at day 3 (fixed dose of 400 mg)
63
Standard of Care -- Severe COVID Population (WHO-CPS =5)
Usual care was provided at the discretion of the clinicians
67
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)
Tocilizumab 8mg/kg on day 1 and if no response (no decrease of oxygen requirement) a second injection at day 3 (fixed dose of 400 mg)
49
Standard of Care -- Critical COVID Population (WHO-CPS >5)
Usual care was provided at the discretion of the clinicians
43
Total222

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003
Overall StudyWithdrew consent1023

Baseline characteristics

CharacteristicTOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Standard of Care -- Severe COVID Population (WHO-CPS =5)TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Standard of Care -- Critical COVID Population (WHO-CPS >5)Total
Age, Continuous64 years63.3 years63.2 years65.4 years64 years
Body Mass Index27.9 kg/m²27.4 kg/m²27.8 kg/m²28.7 kg/m²27.8 kg/m²
Race and Ethnicity Not Collected0 Participants
Sex: Female, Male
Female
19 Participants23 Participants16 Participants10 Participants68 Participants
Sex: Female, Male
Male
44 Participants44 Participants33 Participants33 Participants154 Participants
SPO295 %95 %94 %91 %95 %
Temperature37.3 °c37.9 °c37.7 °c38 °c37.7 °c
Weight80 kg78 kg80 kg81 kg80 kg

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
7 / 6311 / 6712 / 4913 / 43
other
Total, other adverse events
0 / 00 / 00 / 00 / 0
serious
Total, serious adverse events
20 / 6329 / 6731 / 4927 / 43

Outcome results

Primary

Cumulative Incidence (Percentage of Participants) With Successful Tracheal Extubation at Day 14 -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)

Cumulative incidence of successful tracheal extubation (defined as duration extubation \> 48h) at day 14 if patients have been intubated before day 14 ; or removal of Non Invasive Ventilation or high flow (for \> 48h) if they were included under oxygen by Non Invasive Ventilation or High flow (score 6) and remained without intubation. Death or new do-not-resuscitate order (if given after the inclusion of the patient) will be considered as a competing event.

Time frame: Day 1 to Day 14

Population: Critical COVID Population (WHO clinical progression scale \>5 at baseline)

ArmMeasureValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) With Successful Tracheal Extubation at Day 14 -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)47 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) With Successful Tracheal Extubation at Day 14 -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)42 percentage of participants
90% CI: [0.71, 2.04]Bayesian analysis
Primary

Percentage of Participants With no Improvement in WHO Clinical Progression Scale at Day 4 -- Critical COVID Population ( WHO Clinical Progression Scale >5 at Baseline)

Results are presented as the percentage not improved, so that an effective treatment would be associated with a decrease in percentage WHO progression scale: Uninfected; non viral RNA detected: 0 Asymptomatic; viral RNA detected: 1 Symptomatic; Independent: 2 Symptomatic; Assistance needed: 3 Hospitalized; No oxygen therapy: 4 Hospitalized; oxygen by mask or nasal prongs: 5 Hospitalized; oxygen by NIV or High flow: 6 Intubation and Mechanical ventilation, pO2/FIO2\>=150 OR SpO2/FIO2\>=200: 7 Mechanical ventilation, (pO2/FIO2\<150 OR SpO2/FIO2\<200) OR vasopressors (norepinephrine \>0.3 microg/kg/min): 8 Mechanical ventilation, pO2/FIO2\<150 AND vasopressors (norepinephrine \>0.3 microg/kg/min), OR Dialysis OR ECMO: 9 Dead: 10

Time frame: 4 days

Population: Critical COVID population ( WHO Clinical Progression Scale \>5 at baseline)

ArmMeasureValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Percentage of Participants With no Improvement in WHO Clinical Progression Scale at Day 4 -- Critical COVID Population ( WHO Clinical Progression Scale >5 at Baseline)71 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Percentage of Participants With no Improvement in WHO Clinical Progression Scale at Day 4 -- Critical COVID Population ( WHO Clinical Progression Scale >5 at Baseline)70 percentage of participants
90% CI: [-13.6, 17.1]Bayesian analysis
Primary

Percentage of Participants With Non-invasive Ventilation, Mechanical Ventilation or Death at Day 14 (WHO Clinical Progression Scale =5 at Baseline)

Survival without needs of ventilator utilization (including non invasive ventilation and high flow) at day 14. Percentage of non-invasive ventilation, mechanical ventilation or death. Thus, events considered are needing ventilator utilization (mechanical or non-invasive ventilation including high flow oxygen), or death. New do-not-resuscitate (DNR) order (if given after the inclusion of the patient) will be considered as an event at the date of the DNR.

Time frame: Day 1 to Day 14

Population: Severe COVID Population (WHO clinical progression scale =5 at baseline)

ArmMeasureValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Percentage of Participants With Non-invasive Ventilation, Mechanical Ventilation or Death at Day 14 (WHO Clinical Progression Scale =5 at Baseline)24 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Percentage of Participants With Non-invasive Ventilation, Mechanical Ventilation or Death at Day 14 (WHO Clinical Progression Scale =5 at Baseline)36 percentage of participants
90% CI: [0.33, 1]Bayesian analysis
Primary

Percentage of Participants With WHO Clinical Progression Scale > 5 at Day 4 -- Severe COVID Population (WHO Clinical Progression Scale =5 at Baseline)

Percentage of participants who has died or needed non-invasive or mechanical ventilation by day 4 (WHO clinical progression scale \> 5). A patient with new do-not-resuscitate order at day 4 will be considered as with a score \> 5. WHO progression scale: Uninfected; non viral RNA detected: 0 Asymptomatic; viral RNA detected: 1 Symptomatic; Independent: 2 Symptomatic; Assistance needed: 3 Hospitalized; No oxygen therapy: 4 Hospitalized; oxygen by mask or nasal prongs: 5 Hospitalized; oxygen by NIV or High flow: 6 Intubation and Mechanical ventilation, pO2/FIO2\>=150 OR SpO2/FIO2\>=200: 7 Mechanical ventilation, (pO2/FIO2\<150 OR SpO2/FIO2\<200) OR vasopressors (norepinephrine \>0.3 microg/kg/min): 8 Mechanical ventilation, pO2/FIO2\<150 AND vasopressors (norepinephrine \>0.3 microg/kg/min), OR Dialysis OR ECMO: 9 Dead: 10

Time frame: 4 days

Population: Severe COVID Population (WHO clinical progression scale =5 at baseline)

ArmMeasureValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Percentage of Participants With WHO Clinical Progression Scale > 5 at Day 4 -- Severe COVID Population (WHO Clinical Progression Scale =5 at Baseline)19 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Percentage of Participants With WHO Clinical Progression Scale > 5 at Day 4 -- Severe COVID Population (WHO Clinical Progression Scale =5 at Baseline)28 percentage of participants
90% CI: [-21, 3.1]Bayesian analysis
Secondary

Cumulative Incidence (Percentage of Participants) of Discharge From Hospital

Time to discharge from hospital

Time frame: 28, 90 days

Population: No assessment in Severe COVID Population (WHO Clinical Progression Scale =5 at baseline) at Day 90

ArmMeasureGroupValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Discharge From HospitalDay 2883 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Discharge From HospitalDay 2873 percentage of participants
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Discharge From HospitalDay 2855 percentage of participants
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Discharge From HospitalDay 9070 percentage of participants
Standard of Care -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Discharge From HospitalDay 2842 percentage of participants
Standard of Care -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Discharge From HospitalDay 9060 percentage of participants
Comparison: Day 2895% CI: [1.02, 2.27]Fine-Gray model
Comparison: Day 2895% CI: [0.8, 2.63]Fine-Gray model
Comparison: Day 9095% CI: [0.84, 2.17]Fine-Gray model
Secondary

Cumulative Incidence (Percentage of Participants) of Intensive Care Unit Discharge -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)

Time to discharge from Intensive Care Unit

Time frame: 28, 90 days

Population: Critical COVID Population (WHO clinical progression scale \>5 at baseline) Patients in intensive care unit at inclusion

ArmMeasureGroupValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Intensive Care Unit Discharge -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 2872 percentage of participants
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Intensive Care Unit Discharge -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 9084 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Intensive Care Unit Discharge -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 2860 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Intensive Care Unit Discharge -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 9083 percentage of participants
Comparison: Day 2895% CI: [0.73, 1.81]Fine-Gray model
Comparison: Day 9095% CI: [0.73, 2.24]Fine-Gray model
Secondary

Cumulative Incidence (Percentage of Participants) of Oxygen Supply Independency

Time to oxygen supply independency

Time frame: Day 28, 90

Population: No assessment in Severe COVID Population (WHO Clinical Progression Scale =5 at baseline) at Day 90

ArmMeasureGroupValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Oxygen Supply IndependencyDay 2889 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Cumulative Incidence (Percentage of Participants) of Oxygen Supply IndependencyDay 2875 percentage of participants
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Oxygen Supply IndependencyDay 2859 percentage of participants
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Oxygen Supply IndependencyDay 9069 percentage of participants
Standard of Care -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Oxygen Supply IndependencyDay 2849 percentage of participants
Standard of Care -- Critical COVID Population (WHO-CPS >5)Cumulative Incidence (Percentage of Participants) of Oxygen Supply IndependencyDay 9064 percentage of participants
Comparison: Day 2895% CI: [0.98, 2.01]Fine-Gray model
Comparison: Day 2895% CI: [0.82, 2.52]Fine-Gray model
Comparison: Day 9095% CI: [0.8, 2.03]Fine-Gray model
Secondary

Mean of Ventilator Free-days at Day 28 -- Critical COVID Population (WHO-clinical Progression Scale >5 at Baseline)

28-day ventilator free-days

Time frame: 28 days

Population: Critical COVID Population (WHO clinical progression scale \>5 at baseline)

ArmMeasureValue (MEAN)Dispersion
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Mean of Ventilator Free-days at Day 28 -- Critical COVID Population (WHO-clinical Progression Scale >5 at Baseline)12.8 daysStandard Deviation 10.7
Standard of Care -- Severe COVID Population (WHO-CPS =5)Mean of Ventilator Free-days at Day 28 -- Critical COVID Population (WHO-clinical Progression Scale >5 at Baseline)10.3 daysStandard Deviation 11.1
95% CI: [-6.9, 1.7]
Secondary

PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)

Evolution of PaO2/FiO2 ratio PaO2 is partial pressure of arterial oxygen expressed in mmHg. FiO2 is fraction of inspired oxygen (for instance, 0.33 for 33% oxygen) with no units. PaO2/FiO2 ratio is expressed in mmHg.

Time frame: day 1 to day 14

Population: No statistical comparison was performed due to the limited number of patients with available follow-up data.

ArmMeasureGroupValue (MEDIAN)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 1155.1 mmHg
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 4144.0 mmHg
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day7126.0 mmHg
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 14153.7 mmHg
Standard of Care -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 1494.0 mmHg
Standard of Care -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 1135.0 mmHg
Standard of Care -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day7142.8 mmHg
Standard of Care -- Severe COVID Population (WHO-CPS =5)PaO2/FIO2 Ratio -- Critical COVID Population (WHO Clinical Progression Scale >5 at Baseline)Day 4143.8 mmHg
Secondary

Percentage of Participants Surviving (Overall Survival)

Percentage of participants surviving at 14, 28 and 90 days

Time frame: 14, 28 and 90 days

ArmMeasureGroupValue (NUMBER)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Percentage of Participants Surviving (Overall Survival)Day 9089 percentage of participants
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Percentage of Participants Surviving (Overall Survival)Day 1489 percentage of participants
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)Percentage of Participants Surviving (Overall Survival)Day 2889 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Percentage of Participants Surviving (Overall Survival)Day 1491 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Percentage of Participants Surviving (Overall Survival)Day 9084 percentage of participants
Standard of Care -- Severe COVID Population (WHO-CPS =5)Percentage of Participants Surviving (Overall Survival)Day 2888 percentage of participants
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Percentage of Participants Surviving (Overall Survival)Day 2884 percentage of participants
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Percentage of Participants Surviving (Overall Survival)Day 1490 percentage of participants
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)Percentage of Participants Surviving (Overall Survival)Day 9076 percentage of participants
Standard of Care -- Critical COVID Population (WHO-CPS >5)Percentage of Participants Surviving (Overall Survival)Day 1479 percentage of participants
Standard of Care -- Critical COVID Population (WHO-CPS >5)Percentage of Participants Surviving (Overall Survival)Day 9070 percentage of participants
Standard of Care -- Critical COVID Population (WHO-CPS >5)Percentage of Participants Surviving (Overall Survival)Day 2877 percentage of participants
Comparison: Day 1495% CI: [0.4, 3.55]Regression, Cox
Comparison: Day 2895% CI: [0.33, 2.53]Regression, Cox
Comparison: Day 9095% CI: [0.25, 1.65]Regression, Cox
Comparison: Day 1495% CI: [0.12, 1.15]Regression, Cox
Comparison: Day 2895% CI: [0.32, 1.47]Regression, Cox
Comparison: Day 9095% CI: [0.3, 1.49]Regression, Cox
Secondary

WHO Progression Scale

WHO progression scale: Uninfected; non viral RNA detected: 0 Asymptomatic; viral RNA detected: 1 Symptomatic; Independent: 2 Symptomatic; Assistance needed: 3 Hospitalized; No oxygen therapy: 4 Hospitalized; oxygen by mask or nasal prongs: 5 Hospitalized; oxygen by NIV or High flow: 6 Intubation and Mechanical ventilation, pO2/FIO2\>=150 OR SpO2/FIO2\>=200: 7 Mechanical ventilation, (pO2/FIO2\<150 OR SpO2/FIO2\<200) OR vasopressors (norepinephrine \>0.3 microg/kg/min): 8 Mechanical ventilation, pO2/FIO2\<150 AND vasopressors (norepinephrine \>0.3 microg/kg/min), OR Dialysis OR ECMO: 9 Dead: 10

Time frame: 4, 7 and 14 days

Population: Missing data are possible

ArmMeasureGroupValue (MEDIAN)
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)WHO Progression ScaleDay 45 units on a scale
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)WHO Progression ScaleDay 142 units on a scale
TOCILIZUMAB -- Severe COVID Population (WHO-CPS =5)WHO Progression ScaleDay 75 units on a scale
Standard of Care -- Severe COVID Population (WHO-CPS =5)WHO Progression ScaleDay 45 units on a scale
Standard of Care -- Severe COVID Population (WHO-CPS =5)WHO Progression ScaleDay 144 units on a scale
Standard of Care -- Severe COVID Population (WHO-CPS =5)WHO Progression ScaleDay 75 units on a scale
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)WHO Progression ScaleDay 77 units on a scale
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)WHO Progression ScaleDay 47 units on a scale
TOCILIZUMAB -- Critical COVID Population (WHO-CPS >5)WHO Progression ScaleDay 147 units on a scale
Standard of Care -- Critical COVID Population (WHO-CPS >5)WHO Progression ScaleDay 48 units on a scale
Standard of Care -- Critical COVID Population (WHO-CPS >5)WHO Progression ScaleDay 147 units on a scale
Standard of Care -- Critical COVID Population (WHO-CPS >5)WHO Progression ScaleDay 78 units on a scale
Comparison: Day 495% CI: [0.27, 1.28]Proportionnal odds model
Comparison: Day 795% CI: [0.43, 1.71]Proportionnal odds model
Comparison: Day 1495% CI: [0.4, 1.42]Proportionnal odds model
Comparison: Day 495% CI: [0.39, 1.82]Proportionnal odds model
Comparison: Day 795% CI: [0.32, 1.47]Proportionnal odds model
Comparison: Day 1495% CI: [0.32, 1.43]Proportionnal odds model

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026