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
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.
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 →Marius Henriksen is the lead sponsor of 18 studies on the registry; 3 are open to participants now.
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Exclusion Criteria:
Single dose treatment with 400 mg tocilizumab intravensously
Drug: RoActemra iv · Other: Standard medical care
Single dose treatment with 2 x 162 mg tocilizumab subcutaneously
Drug: RoActemra sc · Other: Standard medical care
Single dose treatment with 1 x 200 mg sarilumab subcutaneously
Drug: Kevzara sc · Other: Standard medical care
Management as usual
Other: Standard medical care
single dose treatment with tocilizumab 400 mg intravenously
Also known as: tocilizumab 400 mg
single dose treatment with tocilizumab 2 x 162 mg subcutaneously
Also known as: tocilizumab 2 x 162 mg
single dose treatment with sarilumab 1 x 200 mg subcutaneously
Also known as: sarilumab 1 x 200 mg
management as usual
Time to independence from supplementary oxygen therapy
Time frame: days from enrolment up 28 days
Number of deaths
Time frame: 28 days from enrolment
Days out of hospital and alive
Time frame: 28 days from enrolment
Ventilator free days alive and out of hospital
Time frame: 28 days from enrolment
C-reactive protein (CRP) level
Measured from standard blood test
Time frame: baseline
C-reactive protein (CRP) level
Measured from standard blood test
Time frame: peak during hospitalisation, up to 28 days
C-reactive protein (CRP) level
Measured from standard blood test
Time frame: 14 days
C-reactive protein (CRP) level
Measured from standard blood test
Time frame: 28 days
Number of participants with serious adverse events
Measured as occurrence of any serious adverse events
Time frame: During treatment, up to 28 days
Plan to share: Yes
Supporting information: Study protocol, Sap, Icf, Csr, Analytic code
No publications or documents are linked to this record.
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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Marius Henriksen