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Comparison · NCT04579393-2f0d8dc6

Fostamatinib With Standard of Care for Treatment of COVID-19 vs Placebo With Standard of Care for Treatment of COVID-19: Number of Participants With at Least 1 Serious Adverse Event

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Fostamatinib With Standard of Care for Treatment of COVID-19 vs Placebo With Standard of Care for Treatment of COVID-19: Number of Participants With at Least 1 Serious Adverse Event. Trial comparisons, record NCT04579393-2f0d8dc6. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04579393-2f0d8dc6

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.10.03460.256wilson
Risk in group 20.2070.09850.384wilson
Risk difference, group 1 minus group 2-0.107-0.2960.0833newcombe hybrid score
Risk ratio, group 1 over group 20.4830.1331.75log
Odds ratio, group 1 over group 20.4260.09571.9log
Number needed to treat, for one fewer participant with the outcome on Fostamatinib With Standard of Care for Treatment of COVID-19 than on Placebo With Standard of Care for Treatment of COVID-199.35from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Fostamatinib With Standard of Care for Treatment of COVID-19Fostamatinib, will be administered orally at a dose of 150 mg twice daily for 14 days or 28 doses.330OG000
Group 2Placebo With Standard of Care for Treatment of COVID-19Placebo tablets to match fostamatinib 150 mg will be provided and administered orally at a dose of 150 mg twice daily for 14 days or 28 doses.629OG001

Outcome

Type
PRIMARY
Title
Number of Participants With at Least 1 Serious Adverse Event
Description
Number of participants with at least 1 serious adverse event by day 29 using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. CTCAE is a list of common adverse event (AE) terms. Each AE term is defined and accompanied by a grading scale (1 to 5) that indicates the severity of the AE. Grading ranges from Grade 1 which is mild to Grade 5 which is death.
Time frame
Day 29
Population
Intention-to-treat analysis

Source ClinicalTrials.gov

Trial

Title
Fostamatinib for Hospitalized Adults With COVID-19
NCT number
NCT04579393
Phases
PHASE2
Conditions
Coronavirus Disease 2019
Interventions
Placebo, fostamatinib
Lead sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Results first posted
2022-03-02

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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