Subcutaneous Sarilumab vs Placebo in Hospitalized Patients With Respiratory Distress Caused by COVID 19

NCT ID: NCT07196306

Last Updated: 2025-09-29

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-05-07
• Study Completion Date: 2020-10-15

Brief Summary

Studying the efficacy of IL-6 inhibition utilizing single or double dose subcutaneous administration of Sarilumab in patients with severe respiratory distress caused by COVID19 regarding improvement in oxygen demands and other clinical outcomes.

Detailed Description

At the time of writing this protocol, there does not exist any strategy to treat acute respiratory distress syndrome associated with COVID-19. Due to the overwhelming health crisis facing a large portion of the population, and due to lack of standardization or clinical approach to management of severe respiratory failure short of standard of care with oxygenation and supportive measures, we elected to embark on this study to evaluate the role of IL-6 stimulating the immune system and the effect of inhibiting signal propagation on clinical outcome.

For this study, Sarilumab, an FDA approved IL-6 receptor antagonist, currently used for severe rheumatoid arthritis, has been selected. The dose and administration of therapy used for the study conforms to the current FDA recommendation for the primary use of Sarilumab.

Conditions

COVID; COVID-19; Corona Virus Infection

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Sarilumab

200 mg in 1.14 mL Subcutaneous x 1 or 2 dose(s)

Group Type: EXPERIMENTAL

Sarilumab 200 MG/1.14 ML Subcutaneous Solution

Intervention Type: DRUG

At the time of enrollment, the intervention arm subjects are administered single or double dose of study drug while the placebo arm subjects are administered the placebo drug (normal saline). Subjects will be assigned to the intervention or placebo arm in random order.

Placebo

Normal saline 0.9% 1.14 mL Subcutaneous x 1 or 2 dose(s)

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Normal saline 0.9% 1.14 mL Subcutaneous x 1 or 2 dose(s)

Interventions

Sarilumab 200 MG/1.14 ML Subcutaneous Solution

At the time of enrollment, the intervention arm subjects are administered single or double dose of study drug while the placebo arm subjects are administered the placebo drug (normal saline). Subjects will be assigned to the intervention or placebo arm in random order.

Intervention Type: DRUG

Placebo

Normal saline 0.9% 1.14 mL Subcutaneous x 1 or 2 dose(s)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Confirmed COVID-19 via centralized RT-PCR testing for SARS-CoV2 infection performed at BayCare Health System Laboratory or associated and accredited laboratory.

2. Subjects must be hospitalized.

3. Document fever of 100.4 F or more during hospitalization and prior to enrollment.

4. Evidence of abnormal chest imaging chest x-ray or CT.

5. Moderate to severe respiratory distress requiring oxygen supplementation as defined by criteria listed below.

"Oxygen saturation (Sao2) of 92% or less on room air or a ratio of the partial pressure of oxygen (Pao2) to the fraction of inspired oxygen (Fio2) of less than 200 mm Hg, on ventilator settings that include PEEP ≥5 cm H2O".

6. Subjects may have active co-infection with other respiratory pathogens.

7. Males and non-pregnant females at least 18 years of age.

Exclusion Criteria

1. The subject or Legally Authorized Representative is unable to provide consent in person or by phone.

2. The subject is participating in any other clinical trial for treatment of COVID 19 or any other treatment related clinical trial for a concurrent disease. No plans for additional COVID trials.

3. The subject does not meet criteria for moderate to severe respiratory distress.

4. The presence of any of the following lab abnormalities. ANC <2000/mm3, Platelet count <50,000/mm3, ALT/AST >6x ULN

5. Prior utilization of any IL-6 inhibitors or receptor antagonists at any time in patient's life, JAK inhibitors, DMARDS(Except Hydroxychloroquine), long term, chronic steroid use (more than 6 months) or mTOR inhibitors.

6. The subject has history of organ or bone marrow transplant.

7. History of active or incompletely treated Tuberculosis (TB).

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

BayCare Health System

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Danielle Mauck, BA

Role: STUDY_DIRECTOR

BayCare Health System

Locations

Morton Plant Hospital

Clearwater, Florida, United States

St. Anthony's Hospital

St. Petersburg, Florida, United States

St. Joseph's Hospital

Tampa, Florida, United States

Countries

United States

Other Identifiers

1

Identifier Type: -

Identifier Source: org_study_id