Tocilizumab
DrugParticipants will receive intravenous (IV) tocilizumab
NCT Number: NCT05164133
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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Notify MeUp to 17 year
All sexes
Interventional
Phase 1
Santa Casa de Misericordia de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive intravenous (IV) tocilizumab
Time frame: Through Day 28
Time frame: Through Day 28
Time frame: Days 0-28
Time frame: Day 28
Time frame: Through Day 28
Time frame: Through Day 28
Time frame: Through Day 28
Time frame: Through Day 60
Time frame: Through Day 60
Time frame: Through Day 60
Time frame: Up to 60 days
Time frame: Up to 60 days
Hoffmann-La Roche
Industry
A Phase Ib, Single-Arm, Open-Label Study Evaluating the Pharmacokinetics, Pharmacodynamics, and Safety of Tocilizumab in Pediatric Patients Hospitalized With COVID-19
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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