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TociliuzumabWiki

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Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (0)


Name (Synonyms) Correlation

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D011014 Pneumonia NIH 0.06

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.06

There is one clinical trial.

Clinical Trials


1 A Phase-II, Open-Label, Randomized, Multicenter Study to Investigate the Pharmacodynamics, Pharmacokinetics, Safety, and Efficacy of 8 mg/kg or 4mg/kg Intravenous Tocilizumab in Patients With Moderate to Severe COVID-19 Pneumonia

This study will assess the pharmacodynamics, pharmacokinetics, safety and efficacy of two different doses of tocilizumab (TCZ) in combination with standard-of-care (SOC) in hospitalized adult participants with moderate to severe COVID-19 pneumonia.

NCT04363736 COVID-19 Pneumonia Drug: Tociliuzumab
MeSH:Pneumonia
HPO:Pneumonia

Primary Outcomes

Measure: Serum Concentration of interleukin-6 (IL-6) Following Administration of 8 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Measure: Serum Concentration of Soluble Interleukin-6 Receptor (sIL-6R) Following Administration of 8 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Measure: Serum Concentration of Ferritin Following Administration of 8 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Measure: Serum Concentration of C-reactive Protein (CRP) Following Administration of 8 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Measure: Serum Concentration of IL-6 Following Administration of 4 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Measure: Serum Concentration of sIL-6R Following Administration of 4 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Measure: Serum Concentration of Ferritin Following Administration of 4 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Measure: Serum Concentration of CRP Following Administration of 4 mg/kg IV TCZ

Time: At pre-defined intervals from first TCZ administration to Day 28

Secondary Outcomes

Measure: Pecentage of Participants with Adverse Events

Time: Up to Day 28

Measure: Severe Acute Respiratory Syndrome Corona Virus 2 (SARS-CoV-2) (COVID-19) Viral Load Over Time

Time: Up to Day 28

Measure: Time to Real-Time Polymerase Chain Reaction (RT-PCR) Virus Negativity

Time: Up to Day 28

Measure: Proportion of Participants with any Post-Treatment Infection

Time: Up to Day 28


Related HPO nodes (Using clinical trials)