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TerminatedNCT04322773TOCIVIDUpdated Oct 9, 2020

Anti-il6 Treatment of Serious COVID-19 Disease With Threatening Respiratory Failure

A Phase 2 interventional study of RoActemra iv and RoActemra sc in Corona Virus Disease, sponsored by Marius Henriksen. Terminated at 2 sites in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-10-09.

Sponsored by Marius Henriksen · Phase 2, Interventional, and Treatment

Why this study was terminated
The study has been terminated due to changed clinical conditions and too few patients available
Phase
Phase 2
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Coronavirus disease 2019 (COVID-19) is caused by the newly discovered coronavirus, SARS-CoV-2. The median time from onset of symptoms of COVID-19 to development of acute respiratory distress syndrome (ARDS) has been reported as short as 9 days. No effective prophylactic or post-exposure therapy is currently available. According to data from the Danish Health Authority (www.sst.dk/corona), as of March 21st, 2020, there were 1326 patients infected with the disease in Denmark, more than 250 are admitted to a hospital, and >50 of them have required intensive care. Nearly 350.000 cases and 15.000 deaths have been reported globally. These numbers are likely to markedly increase during the coming weeks, challenging the capacity of health systems worldwide.

In patients infected with SARS-CoV-2, it has been described that disease severity and outcomes are related to the characteristics of the immune response. Interleukin (IL)-6 and other components of the inflammatory cascade contribute to host defense against infections. However, exaggerated synthesis of IL-6 can lead to an acute severe systemic inflammatory response known as 'cytokine storm'. In the pathogenesis of SARS-CoV-2 pneumonia, a study found that a cytokine storm involving a considerable release of proinflammatory cytokines occurred, including IL-6, IL-12, and tumor necrosis factor α (TNF-α). Studies on the Middle East respiratory syndrome caused by another coronavirus (MERS-CoV), indicate that cytokine genes of IL-6, IL-1β, and IL-8 can be markedly upregulated. Similarly, patients with SARS-CoV-2 pneumonia admitted to an intensive care unit had higher plasma levels of cytokines including IL-6, IL-2, IL-7, IL-10, granulocyte-colony stimulating factor (G-CSF), interferon-γ-inducible protein (IP10), monocyte chemoattractant protein (MCP1), macrophage inflammatory protein 1 alpha (MIP1A), and TNF-α. These findings indicate that the magnitude and characteristics of the cytokine response is related to the severity and prognosis of patients with SARS-CoV-2 pneumonia.

It has been suggested that IL-6 blockade may constitute a novel therapeutic strategy for other types of cytokine storm, such as the systemic inflammatory response syndrome including sepsis, macrophage activation syndrome and hemophagocytic lymphohistiocytosis. Remarkable beneficial effects of IL-6 blockade therapy using a IL-6 receptor inhibitor has been described in patients with severe SARS-CoV-2 pneumonia in a retrospective case series from China.

Currently, there are two available drugs based on human monoclonal antibodies against IL-6 receptor, tocilizumab (RoActemra, Roche) and sarilumab (Kevzara, Sanofi). IL-6 receptor inhibitors are currently licensed for several autoimmune disorders and are considered well tolerated and safe in general. The most common side effects reported are upper respiratory tract infections, headache, hypertension, and abnormal liver function tests. The most serious side effects are serious infections, complications of diverticulitis, and hypersensitivity reactions.

it is hypothesized that IL-6 might play a key role in the cytokine storm associated with serious adverse outcomes in patients infected with SARS-CoV-2 pneumonia, and that blockade of IL-6 would be suitable therapeutic target for these patients. The study will investigate the effect of different types of IL-6 inhibition versus no adjuvant treatment compared to standard of care in patients with severe SARS-CoV-2 pneumonia.

Primary objective: To compare the effect of either one of three IL-6 inhibitor administrations, relative to the standard of care, on time to independence from supplementary oxygen therapy, measured in days from baseline to day 28, in patients with severe SARS-CoV-2 pneumonia.

02

Conditions studied

  • Corona Virus Disease

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03

In context

Virus Diseases

914 studies on the registry are indexed under Virus Diseases; 110 are open to participants now.

This study's enrollment of 20 is below the median of 102 across 604 interventional studies indexed under Virus Diseases.

Browse Virus Diseases studies →

Lead sponsor

Marius Henriksen is the lead sponsor of 18 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • SARS-CoV-2 infection confirmed by real time-PCR and
  • Positive imaging: consolidation, ground glass opacities, or bilateral pulmonary infiltration either by CT-scan or chest x-ray; and
  • Need of oxygen therapy to maintain SO2>94% OR FiO2/PaO2 > 20 and at least two of the following laboratory measures:
  • CRP level >70 mg/L
  • CRP level >= 40 mg/L and doubled within 48 hours (without other confirmed infectious or non-infectious course),
  • Lactatdehydrogenase > 250 U/L,
  • thrombocytopenia \< 120.000 x 10E9/L,
  • lymphocyte count \< 0.6 x 10E9/L,
  • D-dimer > 1 ug/mL,
  • serum ferritin > 300 ug/mL

Exclusion criteria

Exclusion Criteria:

  • pregnancy suspected or confirmed,
  • severe heart failure,
  • suspected or confirmed bacterial infection,
  • current solid or hematological malignancy,
  • neutropenia,
  • ALAT elevation more than three times the laboratory upper limit,
  • ASA class 5 (after COVID19 admission) or higher at inclusion (prior admission),
  • severe chronic obstructive pulmonary disease or heart failure (NYHA class II or higher),
  • pregnant or lactating women,
  • current treatment with conventional synthetic disease-modifying antirheumatic drugs (DMARDs)/immunosuppressive agents including IL-6 inhibitors, or with Janus kinase inhibitors (JAKi) in the past 30 days or plans to receive during the study period,
  • current use of chronic oral corticosteroids in a dose higher than prednisone 10 mg or equivalent per day,
  • previous or active tuberculosis (TB),
  • HIV infection regardless of immunological status, hepatitis,
  • evidence of recent (30 days) invasive bacterial or fungal infections,
  • patients who have received immunosuppressive antibody therapy within the past 5 months, including intravenous immunoglobulin or plans to receive during the study period,
  • IV drug abuse,
  • history of inflammatory bowel disease,
  • diverticulitis,
  • ulcer,
  • perforated gastrointestinal tract,
  • participation in any clinical research study evaluating an investigational product (IP) or therapy within 3 months and less than five half-lives of IP prior inclusion to the study,
  • any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the patient by their participation in the study,
  • inability to give informed consent.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Roactemra iv

    Single dose treatment with 400 mg tocilizumab intravensously

    Drug: RoActemra iv · Other: Standard medical care

  • Experimental
    Roactemra sc

    Single dose treatment with 2 x 162 mg tocilizumab subcutaneously

    Drug: RoActemra sc · Other: Standard medical care

  • Experimental
    Kevzara sc

    Single dose treatment with 1 x 200 mg sarilumab subcutaneously

    Drug: Kevzara sc · Other: Standard medical care

  • Active comparator
    Standard care

    Management as usual

    Other: Standard medical care

Interventions

  • DrugRoActemra iv

    single dose treatment with tocilizumab 400 mg intravenously

    Also known as: tocilizumab 400 mg

  • DrugRoActemra sc

    single dose treatment with tocilizumab 2 x 162 mg subcutaneously

    Also known as: tocilizumab 2 x 162 mg

  • DrugKevzara sc

    single dose treatment with sarilumab 1 x 200 mg subcutaneously

    Also known as: sarilumab 1 x 200 mg

  • OtherStandard medical care

    management as usual

06

What researchers measure

Primary outcomes

  1. Time to independence from supplementary oxygen therapy

    Time frame: days from enrolment up 28 days

Secondary outcomes

  1. Number of deaths

    Time frame: 28 days from enrolment

  2. Days out of hospital and alive

    Time frame: 28 days from enrolment

  3. Ventilator free days alive and out of hospital

    Time frame: 28 days from enrolment

  4. C-reactive protein (CRP) level

    Measured from standard blood test

    Time frame: baseline

  5. C-reactive protein (CRP) level

    Measured from standard blood test

    Time frame: peak during hospitalisation, up to 28 days

  6. C-reactive protein (CRP) level

    Measured from standard blood test

    Time frame: 14 days

  7. C-reactive protein (CRP) level

    Measured from standard blood test

    Time frame: 28 days

  8. Number of participants with serious adverse events

    Measured as occurrence of any serious adverse events

    Time frame: During treatment, up to 28 days

07

Study locations

2 sites
  • Bispebjerg-Frederiksberg Hospital
    Copenhagen, 2000, Denmark
  • Hillerød Hospital
    Hillerød, Denmark
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 9, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04322773
Lead sponsor
Marius Henriksen
Responsible party
Marius Henriksen (Professor, Frederiksberg University Hospital) — Sponsor-investigator
First posted
Mar 26, 2020
Start date
Apr 5, 2020
Primary completion
Oct 8, 2020
Completion
Oct 8, 2020
Last update
Oct 9, 2020

Study contacts

Lars Erik Kristensen, PhD
principal investigator · The Parker Institute

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Oct 2020. You cannot join it, but the record below documents what was studied.

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