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Comparison · NCT05593770-da8be995

Fostamatinib vs Placebo: 60-day Mortality

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 vs Placebo: 60-day Mortality. Trial comparisons, record NCT05593770-da8be995. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05593770-da8be995

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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 10.07690.01370.333wilson
Risk in group 20.1670.0470.448wilson
Risk difference, group 1 minus group 2-0.0897-0.3780.193newcombe hybrid score
Risk ratio, group 1 over group 20.4620.04774.46log
Odds ratio, group 1 over group 20.4170.03285.3log
Number needed to treat, for one fewer participant with the outcome on Fostamatinib than on Placebo11.1from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Fostamatinib
An investigational oral spleen tyrosine kinase inhibitor.~Fostamatinib: Fostamatinib100-150mg orally twice daily for 14 days or 28 doses. Study medication will be continued as an outpatient if the patient is discharged prior to completing 28 doses.
113OG000
Group 2Placebo
Orange film-coated, plain, bioconvex tablets for fostamatinib.~For the purposes of interim and final analyses, the route and frequency of placebo will be ignored, and all placebo participants will be pooled together as a single group. In comparing an active drug versus placebo, only those placebo participants that were eligible for the active drug will be included.~Placebo: Orange film-coated, plain bioconvex tablets orally twice daily for 14 days or 28 doses for fostamatinib. Study medication will be continued as an outpatient if the patient is discharged prior to completing 28 doses.
212OG001

Outcome

Type
SECONDARY
Title
60-day Mortality
Description
Number of patients who have died at Day 60
Time frame
Day 60
Population
Participants who lacked outcome data were not included in the analysis. Ineligible participants or those who didn't receive the treatment were excluded.

Source ClinicalTrials.gov

Trial

Title
International Sites: Novel Experimental COVID-19 Therapies Affecting Host Response
NCT number
NCT05593770
Phases
PHASE2, PHASE3
Conditions
COVID-19, SARS-CoV2 Infection, Coronavirus Infection
Interventions
Fostamatinib, Placebo
Lead sponsor
NEAT ID Foundation
Results first posted
2024-11-05

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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