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Comparison · NCT04160468-deaths

Exebacase + SoCA vs SoCA Alone: deaths from any cause

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. Exebacase + SoCA vs SoCA Alone: deaths from any cause. Trial comparisons, record NCT04160468-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04160468-deaths

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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 10.1640.1150.228wilson
Risk in group 20.1650.1010.258wilson
Risk difference, group 1 minus group 2-0.00107-0.1060.0894newcombe hybrid score
Risk ratio, group 1 over group 20.9940.5511.79log
Odds ratio, group 1 over group 20.9920.492.01log
Number needed to treat, for one fewer death from any cause on Exebacase + SoCA than on SoCA Alone935from 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 1Exebacase + SoCAParticipants received a single IV infusion of exebacase in addition to standard-of-care antibiotics (SoCA) selected by the investigator.27165EG000
Group 2SoCA AloneParticipants received a single IV infusion of placebo in addition to standard-of-care antibiotics (SoCA) selected by the investigator.1485EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Through the Day 60 visit

Source ClinicalTrials.gov

Trial

Title
Direct Lysis of Staph Aureus Resistant Pathogen Trial of Exebacase
NCT number
NCT04160468
Phases
PHASE3
Conditions
Staphylococcus Aureus Bacteremia, Staphylococcus Aureus Endocarditis
Interventions
Exebacase, Placebo
Lead sponsor
ContraFect
Results first posted
2023-10-18

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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