Official Title
Tocilizumab: A Therapeutic Cache Against the Treatment of Severe Cases of COVID-19
Brief Summary

The most accepted description of severe COVID-19 disease is development and over production of pro-inflammatory cytokines. Autopsy studies have been done on COVID-19 patients proved that severe disease is resulted due to deviant host-immune response and cytokine storm. Elevated inflammatory biomarkers like C-Reactive protein (CRP) and pro-inflammatory cytokines shown to be higher in severe disease of COVID-19. Several studies on severe COVID-19 have revealed raised levels of plasma cytokines like IL-6, IL-2, IL-10, Gamma interferon (INF), Tumor necrosis factor Alpha TNF. The Cytokines release syndrome (CRS) is a hyperinflammatory deadly syndrome characterized by release of uncontrolled immune system activation which is responsible for multi-organ failure. It has the main role in ARDS due to SARS-CoV-2 virus which binds to alveolar epithelium and resulting in IL-6 release that is responsible for increase alveolar-epithelium permeability. In many studies it has been observed that IL-6 have played a main role in CRS induction. Previous experiences from hyperinflammatory and cytokine storm syndromes recommends that early involvement of inhibiting CRS is essential to prevent lethal tissue damage and poor clinical outcome. In this scenario the judgement of clinical specialist who are suggesting that evidence of CRS can be cured with glucocorticoids, I/V immunoglobulin and anti-cytokine therapy cannot be ignored.

Detailed Description

This is intervention single-center study, that will be done at Lahore General Hospital in
which 95 beds are allocated for COVID-19 patients including ICUs and HDUs. Ethical approval
will be obtained from research ethical committee of Lahore General hospital, Lahore. Informed
consent will be obtained from all patients who will agree to publish their data in this
research. Patient's privacy and obey will be protected with the Helsinki Declaration.

Unknown status
SARS-CoV Infection

Drug: Tocilizumab

4-8mg/kg with 400mg maximum dose of Tocilizumab will be given in 60 minutes I/V infusion, and dose will be repeated after 12-24 hours according to clinical as well as laboratory parameters.
Customized decision for Tocilizumab usage will be made by attending infectious diseases physician, comfort with Tocilizumab usage, bacterial co-infection and duration of Ventilation.
Other Name: ACTEMRA®

Eligibility Criteria

Inclusion Criteria:

- All patients of all ages, males and non-pregnant females who will be diagnosed
COVID-19 positive by RT-PCR.

- Patients having classical radiological lesions of COVID-19 on X-ray chest or HRCT
chest.

- Patient >55 years of age Or Age <55 with comorbid condition who will be unable to
maintain O2 sat > 93% with 5-7 liter of oxygen.

- Or Patient < 55 with no comorbid conditions, who will be unable to maintain O2 sat >
93% with 7-10 liter of oxygen.

- Respiratory rate > 30-35/ min and >50% of radiological involvement of lung with
typical lesions.

- Along with > 50% deranged ≥ 2 biochemical markers CRP > 50 mg/l, LDH > 1000U/L,
D.Dimer > 1mg/l or 1000 ng/ml, Serum Ferritin > 1000 ng/ml or mcg/l will be included
in clinical trial.

Exclusion Criteria:

- Patient who will not require supplemental oxygen during hospital stay.

- Patients on Invasive mechanical ventilation (IMV).

- Patients with respiratory rate < 30/mins and whose laboratory findings will not be
deranged > 50%.

- Patients with improving radiological findings will be excluded.

- Patients suffering from Active TB

- Herpes zoster

- Multiple sclerosis,

- Allergic to tocilizumab

- Presences of chronic renal failure > 4 stage, GFR < 30ml/min/1.73m2.

- ALT/AST > 5 times than normal values.

- Presences of neutropenia < 500/mm3.

- Platelets count less than 50 ×103 /µl.

- Complicated diverticulitis/ intestinal perforation.

- Immune-suppressive anti- rejection therapy.

- Pregnant women.

- Previous MI/ IHD, IV heart failure.

- Psychiatric patients.

Eligibility Gender
All
Eligibility Age
Minimum: 15 Years ~ Maximum: 80 Years
Countries
Pakistan
Locations

Lahore General Hospital
Lahore, Punjab, Pakistan

Investigator: Muhammad Irfan malik
Contact: 03334367220
drmirfanmalik@hotmail.com

Contacts

Muhammad Irfan Malik
03334367220
drmirfanmalik@hotmail.com

Sardar Al-Fareed Zafar, Study Director
Post-Graduate Medical Institute, Lahore General Hospital, Lahore Pakistan

Lahore General Hospital
NCT Number
Keywords
Covid-19
IL-6 Inhibitor
MeSH Terms
COVID-19
Severe Acute Respiratory Syndrome