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OpenTrials
Completed

NCT Number: NCT05164133

A Study Evaluating Tocilizumab in Pediatric Patients Hospitalized With COVID-19

This is a single-arm, open-label study to assess the pharmacokinetics, pharmacodynamics, safety, and exploratory efficacy of tocilizumab (TCZ) for the treatment of pediatric patients from birth to less than 18 years old hospitalized with COVID-19 and who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation.

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Key information

Age range

Up to 17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Santa Casa de Misericordia de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hospitalized with COVID-19 confirmed per a positive PCR of any specimen (e.g., respiratory, blood, urine, stool, or other bodily fluid) and evidenced by chest x-ray or CT scan
  • Receiving systemic corticosteroids at baseline
  • Oxygen saturation < 93% on room air, or requiring supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO) to maintain oxygen saturation > 92% at screening and baseline

Exclusion criteria

  • Gestational age < 37 weeks
  • Known severe allergic reactions to TCZ or other monoclonal antibodies
  • Active tuberculosis infection
  • Uncontrolled active bacterial, fungal, viral, or other infection (besides COVID-19)
  • Diagnosis or suspected diagnosis of multisystem inflammatory syndrome in children (MIS-C)
  • In the opinion of the investigator, progression to death is imminent and inevitable within the next 48 hours, irrespective of the provision of treatments
  • Have received oral anti-rejection or immunomodulatory drugs (including TCZ) within the past 3 months prior to enrollment
  • Treatment with an investigational drug within 5 drug-elimination half-lives or 30 days, whichever is longer, of enrollment (except for anti-SARS-CoV-2 antibodies or directly-acting antivirals)
  • Participating in another interventional drug clinical trial (except for anti-SARS-CoV-2 antibodies or directly-acting antivirals)

Treatment and study plan

Tocilizumab

Drug

Participants will receive intravenous (IV) tocilizumab

Primary outcomes

  1. Serum concentration of TCZ

    Time frame: Through Day 28

  2. Maximum serum concentration (Cmax) of TCZ

    Time frame: Through Day 28

  3. Area under the curve from Days 0-28 (AUC days 0-28) of TCZ

    Time frame: Days 0-28

  4. Serum concentration on Day 28 (C day 28) of TCZ

    Time frame: Day 28

  5. Clearance (CL) of TCZ

    Time frame: Through Day 28

  6. Volume of distribution of TCZ

    Time frame: Through Day 28

Secondary outcomes

  1. Duration of 90% saturation of sIL-6R

    Time frame: Through Day 28

  2. Concentration of IL-6

    Time frame: Through Day 60

  3. Concentration of sIL-6R

    Time frame: Through Day 60

  4. Concentration of C-reactive protein (CRP)

    Time frame: Through Day 60

  5. Percentage of participants with adverse events

    Time frame: Up to 60 days

  6. Percentage of participants with severe adverse events

    Time frame: Up to 60 days

Sponsors and collaborators

Lead sponsor

Hoffmann-La Roche

Industry

Registry information

Official study title

A Phase Ib, Single-Arm, Open-Label Study Evaluating the Pharmacokinetics, Pharmacodynamics, and Safety of Tocilizumab in Pediatric Patients Hospitalized With COVID-19

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Dec 20, 2021
Registry last updated
Apr 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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