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Comparison · NCT04817332-00c708bf

Brensocatib vs Placebo: Improvement of One Category From Admission Using 7-point Ordinal Scale.

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. Brensocatib vs Placebo: Improvement of One Category From Admission Using 7-point Ordinal Scale. Trial comparisons, record NCT04817332-00c708bf. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04817332-00c708bf

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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 10.8370.7780.883wilson
Risk in group 20.8690.8170.908wilson
Risk difference, group 1 minus group 2-0.0323-0.1030.0368newcombe hybrid score
Risk ratio, group 1 over group 20.9630.8871.04log
Odds ratio, group 1 over group 20.7720.4441.34log
Number needed to treat, for one fewer participant with the outcome on Brensocatib than on Placebo30.9from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1BrensocatibBrensocatib oral tablet, 25mg once per day for 28 days~Brensocatib: Selective, competitive, and reversible inhibitor of DPP1159190OG000
Group 2PlaceboPlacebo oral tablet, 25mg once per day for 28 days~Placebo: Matched placebo186214OG001

Outcome

Type
SECONDARY
Title
Improvement of One Category From Admission Using 7-point Ordinal Scale.
Description
Evaluation of the clinical efficacy of Brensocatib relative to standard care: 7-point ordinal scale, minimum value 1, maximum value 7. Higher values indicate a worse outcome:~1. Not hospitalised, no limitations on activities~2. Not hospitalised, limitations on activities~3. Hospitalised, not requiring supplemental oxygen~4. Hospitalised, requiring supplemental oxygen~5. Hospitalised, on non-invasive ventilation or high flow oxygen devices~6. Hospitalised, on invasive mechanical ventilation or Extracorporeal membrane oxygenation (ECMO)~7. Death
Time frame
Day 29
Population
ITT. Days to improvement was derived as~1. days from randomization to date of first follow-up day where there was an improvement in CSTAT~2. those who died before improvement were censored at date of death.~3. those who withdrew or were loss to follow-up before improvement, if their day 29 status was unknown, they were censored at the date of loss to follow-up/withdrawal~4. other participants were censored at day 29 from randomisation in study time if there were no improvement.

Source ClinicalTrials.gov

Trial

Title
STOP-COVID19: Superiority Trial Of Protease Inhibition in COVID-19
NCT number
NCT04817332
Phases
PHASE3
Conditions
Covid19
Interventions
Brensocatib, Placebo
Lead sponsor
University of Dundee
Results first posted
2023-08-22

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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